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What changed in Scienture Holdings, Inc.'s 10-K2023 vs 2024

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Paragraph-level year-over-year comparison of Scienture Holdings, Inc.'s 2023 and 2024 10-K annual filings, covering the Business, Risk Factors, Legal Proceedings, Cybersecurity, MD&A and Market Risk sections. Every new, removed and edited paragraph is highlighted side-by-side so you can see exactly what management changed in the 2024 report.

+1063 added396 removedSource: 10-K (2025-03-26) vs 10-K (2024-04-22)

Top changes in Scienture Holdings, Inc.'s 2024 10-K

1063 paragraphs added · 396 removed · 46 edited across 8 sections

Item 1. Business

Business — how the company describes what it does

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Item 1. Business ”, above, our business is highly regulated in the United States, at both the federal and state level, and in foreign countries. If we fail to comply with regulatory requirements, or if allegations are made that we fail to comply, our results of operations and financial condition could be adversely affected.
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ITEM 1. BUSINESS INTRODUCTION This information included in this Annual Report should be read in conjunction with the consolidated financial statements and related notes in “Item 8. Financial Statements and Supplemental Data” of this Annual Report. Our logo and some of our trademarks and tradenames are used in this Annual Report.
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To lawfully operate our businesses, we are required to obtain, and hold permits, product registrations, licenses and other regulatory approvals from, and to comply with operating and security standards of, numerous governmental bodies..
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This Annual Report may also include trademarks, tradenames and service marks that are the property of others. Solely for convenience, trademarks, tradenames and service marks referred to in this Annual Report may appear without the ®, ™ and SM symbols.
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Failure to maintain or renew necessary permits, product registrations, licenses or approvals, or to comply with required standards, could have an adverse effect on our results of operations and financial condition. We are also required to comply with various state pricing gouging laws. Products that we source and distribute must also comply with regulatory requirements.
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References to our trademarks, tradenames and service marks are not intended to indicate in any way that we will not assert to the fullest extent under applicable law our rights or the rights of the applicable licensors if any, nor that respective owners to other intellectual property rights will not assert, to the fullest extent under applicable law, their rights thereto.
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Noncompliance or concerns over noncompliance may result in suspension of our ability to distribute or import products, product bans, recalls or seizures, or criminal or civil sanctions, which, in turn, could result in product liability claims and lawsuits, including class actions.
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We do not intend the use or display of other companies’ trademarks and trade names to imply a relationship with, or endorsement or sponsorship of us by, any other companies.
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Many of our competitors are better established and have resources significantly greater than we have, which may make it difficult to fend off competition. We expect to compete with large ADR distributors (such as McKesson, Cardinal Health and AmerisourceBergen), in addition to other pharmaceutical distributors, buying groups, software products, and various start-up drug companies.
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The market data and certain other statistical information used throughout this Annual Report are based on independent industry publications, reports by market research firms or other independent sources that we believe to be reliable sources.
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Many of these companies have substantially greater financial and manufacturer-backed resources, longer operating histories, greater name recognition and more established relationships in the industry than us. In addition, a number of these competitors may combine or form strategic partnerships.
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Industry publications and third-party research, surveys and studies generally indicate that their information has been obtained from sources believed to be reliable, although they do not guarantee the accuracy or completeness of such information.
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As a result, our competitors may establish a more favorable footing in the pharmaceutical industry with respect to pricing or other factors.
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We are responsible for all of the disclosures contained in this Annual Report , and we believe these industry publications and third-party research, surveys and studies are reliable.
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Our failure to compete successfully with any of these companies would have a material adverse effect on our business and the trading price of our common stock. 23 The three distributors listed above have a strong control over our industry, as they have contracts with approximately 24,000 independent, retail pharmacies that limit the participants’ ability to purchase pharmaceuticals outside of those primary distributors.
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While we are not aware of any misstatements regarding any third-party information presented in this Annual Report, their estimates, in particular, as they relate to projections, involve numerous assumptions, are subject to risks and uncertainties, and are subject to change based on various factors, including those discussed under the section entitled “Risk Factors” of this Annual Report.
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Additional restrictive elements exist within the pharmaceutical channels of distribution. For example, a number of the inventory management systems, either developed by the distributors or third-party vendors, have been developed to require compliance to these restrictive purchasing agreements.
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These and other factors could cause our future performance to differ materially from our assumptions and estimates. Some market and other data included herein, as well as the data of competitors as they relate to us, are also based on our good faith estimates. Our fiscal year ends on December 31st.
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Management anticipates that other existing and prospective competitors will adopt technologies or business plans similar to ours or seek other means to develop operations competitive with ours, particularly if our development of large-scale production progresses as scheduled. We will need to expand our member base or our profit margins to attain profitability.
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Interim results are presented on a quarterly basis for the quarters ended March 31st, June 30th, and September 30th, the first quarter, second quarter and third quarter, respectively, with the quarter ending December 31st being referenced herein as our fourth quarter.
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Currently, we are aware of the competitiveness of the group of suppliers that participate within our industry and intend to price products accordingly. However, price is not the only factor that influences where retail pharmacies will obtain their product. Quality fulfillment services are also important, and retail pharmacies have historically received quality fulfillment services from the three major ADR distributors.
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“Fiscal 2024” means the Fiscal year ended December 31, 2024, whereas “Fiscal 2023” means the year ended December 31, 2023. Unless the context requires otherwise, references to the “Company,” “we,” “us,” and “our” refer specifically to Scienture Holdings, Inc., formerly known as TRxADE HEALTH, INC., and its consolidated subsidiaries.
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In order to be more competitive, we must improve our customer service and fulfillment efforts, because the independent retail pharmacy has for years considered this element of the fulfillment process as important as price.
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In addition, unless the context otherwise requires and for the purposes of this Annual Report only: ● “Exchange Act” refers to the Securities Exchange Act of 1934, as amended; ● “SEC” refers to the United States Securities and Exchange Commission; and ● “Securities Act” refers to the Securities Act of 1933, as amended.
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Other factors influencing the pharmacies purchasing behavior in the future will be changes brought upon by the ACA, which regulates some aspects of pharmaceutical spending and pricing. Management believes that we should benefit substantially from our pricing and product knowledge that is offered by our platform.
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Available Information We file annual, quarterly, and current reports, proxy statements and other information with the SEC.
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Profitability may be further increased as a result of lower cost of goods, should the Company build stronger relationships with manufacturers and other larger buying groups that serve wholesalers and distributors. On a larger scale, those margins are expected to drop depending upon the breadth of products provided in the market and the sale turn rates required.
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Our SEC filings are available to the public over the Internet at the SEC’s website at http://www.sec.gov and are available for download, free of charge, soon after such reports are filed with or furnished to the SEC, on the “Investors” page of our website at www.scientureholdings.com.
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We are currently undertaking a significant effort to increase our membership base through attendance at annual conferences and other strategies. We intend to expand our e-mail marketing strategy based on our competitive price advantages and unique distribution services. There are inherent risks associated with our operations within the Pharmaceutical Distribution Market.
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Copies of documents filed by us with the SEC are also available from us without charge, upon oral or written request to our Secretary, who can be contacted at the address and telephone number set forth on the cover page of this Annual Report. Our website addresses are www.scientureholdings.com, www.scienture.com, www.trxadehealth.com and www.rxintegra.com.
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There are inherent risks involved with doing business within the pharmaceutical distribution market, including: ● Improperly manufactured products may prove dangerous to the end consumer. ● Products may become adulterated by improper warehousing methods or modes of shipment. ● Counterfeit products or products with fake pedigree papers. ● Unlicensed or unlawful participants in the distribution channel. ● Risk with default and the assumption of credit loss. ● Regulatory risks. ● Risk related to the loss of supply, or the loss of a number of suppliers, or in the delay of obtaining the supply of drugs.
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Information on our websites is not incorporated by reference into this Annual Report.
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Although all of our end-user agreements require our customers to indemnify us and for any and all liabilities resulting from our participation in the pharmaceutical distribution industry, we cannot assure you that the parties required to provide such indemnification will have the financial resources to do so.
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The information on, or that may be accessed through, our websites not incorporated by reference into this Annual Report and should not be considered a part of this Annual Report. 5 Table of Contents Current Business – Scienture LLC Overview Scienture LLC was originally incorporated in Delaware and commenced operations in 2019.
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Additionally, although we have evaluated appropriate state statutes and federal laws pertaining to pharmaceutical distribution in an effort to diminish our risks, the Board of Pharmacy for each state is responsible for interpreting their state laws, and their interpretations may not comport with our analysis.
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In connection with our acquisition in July 2024, Scienture LLC became a wholly owned subsidiary of the Company. Scienture’s principal executive offices are located in Commack, New York. Scienture LLC is a specialty pharmaceutical company focused on developing and commercializing products for the treatment of CNS and CVS diseases.
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It is also possible that any third-party logistics arrangements may disrupt service, create a loss of income, or other unforeseen disruptions should the service provider experience any legal, financial or other difficulties of their own. We do not have a traditional credit facility with a financial institution, which may adversely impact our operations.
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Scienture LLC is developing a broad range of novel product candidates including new potential treatments for hypertension, migraine, pain and thrombosis and other related disorders. Scienture LLC’s Strategy Scienture LLC’s mission is to improve the lives of patients suffering from CNS and CVS diseases.
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We do not have a traditional credit facility with a financial institution, such as a working line of credit. The absence of such a facility could adversely impact our operations, as it may constrain our ability to have available the working capital for equipment purchases or other operational requirements.
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Scienture LLC’s vision is to be a leader in the industry by developing and commercializing new medicines for the treatment of CNS and CVS diseases. Key elements of Scienture LLC’s strategy to achieve this vision include: ● Advance product candidates through clinical studies and toward commercialization.
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If adequate funds are not otherwise available, we may be required to delay, scale back or eliminate portions of our business development efforts.
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Scienture LLC is in various stages of clinical development for the product candidates in its pipeline, and it intends to move these programs efficiently toward being commercially available to patients, subject to approval by the U.S. Food and Drug Administration (the “FDA”).
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Without credit facilities, we could be forced to cease operations and investors in our securities could lose their entire investment. 24 We offer limited credit to the pharmacies which limits the amount of the orders that they place and may result in us losing business and a reduction in our revenues.
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Scienture LLC has obtained regulatory approval of its first product candidate, SCN-102. 6 Table of Contents ● Drive growth and profitability.
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We currently offer a limited amount of credit to our members. Such limited credit reduces the risk that such members do not pay for products; however, it also limits the amount of revenue we generate per member.
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Using dedicated sales and marketing resources in the U.S., which Scienture LLC is in the process of building, Scienture LLC will seek to drive the revenue growth of its product candidates approved for marketing by the FDA. ● Continue to grow pipeline.
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We believe that if we were to increase the amount of credit we provide to members we would generate more revenues, but bear more risk of non-payment. We are currently exploring increasing the amount of credit we provide to members, which may in turn result in an increase in receivables and write-offs.
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Scienture LLC will continue to evaluate and seek to develop additional product candidates that it believes have significant commercial potential through Scienture LLC’s internal research and development efforts. ● Target strategic business development opportunities. Scienture LLC is exploring a broad range of strategic opportunities.
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We are dependent upon our current management, who may have conflicts of interest. We are dependent upon the efforts of our current management. All of our officers and directors have duties and affiliations with other companies.
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This may include in-licensing products and entering into co-promotion and co-development partnerships for Scienture LLC’s product candidates, although no agreements have been reached. Research and Development and Product Portfolio Scienture LLC is committed to the development of innovative product candidates in the CNS and CVS therapeutic areas.
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Even though these companies are not competitors or involved in pharmaceutical distribution, involvement of our officers and directors in other businesses may still present a conflict of interest regarding decisions they make for Trxade or with respect to the amount of time available for Trxade. The loss of any of our officers or directors and, in particular, Mr.
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The process by which Scienture LLC intends to bring its product candidates to market and the anticipated launch dates of its product candidates is depicted in the following table. The progress of Scienture LLC’s products through this process is represented by checkmarks in the table.
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Prashant Patel, our President or Mr. Suren Ajjarapu, our Chief Executive Officer and Chairman of the Company, could have a materially adverse effect upon our business and future prospects. The Company holds, on behalf of and for the benefit of Mr. Suren Ajjarapu, a personal disability insurance policy providing for a $1,500,000 lump sum benefit, payable to Mr.
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Scienture LLC does not have any product candidates approved for sale and has not generated any revenue from product sales. Scienture LLC will not generate revenue from product sales unless and until it successfully obtains regulatory approval for its product candidates.
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Ajjarapu, in the event of Mr. Ajjarapu’s disability. The premiums on such policy will be paid by the Company for so long as Mr. Ajjarapu is employed by the Company. The Company also holds a $4,000,000 key-man life insurance policy on the life of Mr. Suren Ajjarapu, and a $1,500,000 lump sum disability insurance policy on Mr.
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Scienture LLC is engaged in a variety of research and development efforts including development of a pipeline of novel product candidates for the treatment of various disease conditions.
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Ajjarapu, providing for the Company as beneficiary of such policies. While our management team has considerable information technology and entrepreneurial experience, none of our management was involved in pharmaceutical distribution prior to joining the Company and, as such, did not have any technical experience in pharmaceutical distribution prior to joining us. In the event of the loss of Mr.
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Scienture LLC has devoted and will continue to devote significant resources to research and development activities, and expects to incur significant expenses as Scienture LLC continues advancing its product candidates towards FDA approval and expanding product indications for approved products and its intellectual property portfolio.
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Ajjarapu’s services, we will seek to hire and retain a qualified professional. In the event of the loss of his services in connection with his death, upon obtaining funding from the key-man life insurance, management intends to hire qualified and experienced personnel. We may be unable to find a suitable or qualified replacement for Mr.
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Scienture LLC’s expectations regarding its research and development programs are subject to risks, including the risk that Scienture LLC’s financial condition and results of operations for fiscal year 2024 and beyond may be materially and adversely affected by delays and failures in the completion of clinical development of its product candidates, which could increase its costs or delay or limit our ability to generate revenues.
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Ajjarapu and as such our operations and/or prospects may suffer. We rely on third party contracts. We depend on others to provide products and services to us. We do not manufacture pharmaceuticals and we do not sell pharmaceuticals to the end consumer.
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SCN-102 (ARBLI TM - Losartan Oral Suspension) SCN-102 is an oral liquid formulation of losartan potassium in development under the 505(b)(2) pathway, for (i) treatment of hypertension, to lower blood pressure in adults and children greater than 6 years old, (ii) reduction of the risk of stroke in patients with hypertension and left ventricular hypertrophy, and (iii) treatment of diabetic nephropathy with an elevated serum creatinine and proteinuria in patients with type 2 diabetes and a history of hypertension.
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We do not control these wholesalers, suppliers and purchasers, and although our arrangements with them will be terminable or of limited length, a change may be difficult to implement. At this time, we have a working relationship with over 10 manufacturers and other suppliers.
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Currently, there are no FDA-approved liquid formulations of losartan potassium. 7 Table of Contents A Phase I PK study has shown that SCN-102 has close comparability to the immediate-release tablet as depicted in the data below: Summary of Statistical Results for Losartan Potassium Oral Liquid 10 mg/ml (T) versus Losartan Potassium Immediate Release Tablets 100 mg (R) – For Losartan Geometric Means of treatment: Ratio Intra-subject 90% SABE Result – SABE PK Parameter N Test (T) Reference (R) (%) %CV CI of Ratio Bound SWR Log C max (ng/ml) 44 1317.6955 974.6741 135.19 39.6 122.19 – 149.58 0.070 0.3361 LogAUC 0-t (ng.hr/ml) 44 1590.6271 1581.0602 100.61 13.2 97.25 – 104.08 -0.014 0.1576 LogAUC 0-inf (ng.hr/ml) 44 1615.4717 1605.3052 100.63 13.0 97.34 – 104.03 -0.014 0.1549 Summary of Statistical Results for Losartan Potassium Oral Liquid 10 mg/ml (T) versus Losartan Potassium Immediate Release Tablets 100 mg (R) – For Carboxylic Acid Metabolite Geometric Means of treatment: Ratio Intra-subject 90% SABE Result – SABE PK Parameter N Test (T) Reference (R) (%) %CV CI of Ratio Bound SWR Log C max (ng/ml) 44 1160.0978 1056.3253 109.82 25.5 102.91 – 117.20 -0.028 0.2828 LogAUC 0-t (ng.hr/ml) 44 6775.8841 6726.8952 100.73 10.3 98.11 – 103.42 -0.006 0.1099 LogAUC 0-inf (ng.hr/ml) 44 6872.6739 6823.3736 100.72 10.2 98.13 – 103.39 -0.006 0.1071 Specifically, the Phase I PK study showed that SCN-102 was comparable to immediate release tablets based on the following: ● The overall exposure for the Carboxylic Acid metabolite (EXP-3174) meet the confidence interval 80-125% range. ● The overall exposure for Losartan were within the 90% confidence interval. ● The Cmax for Losartan analyte, a pro-drug, for SCN-102 was slightly higher than the immediate release tablets (122.19 - 149.58%).
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Although we believe that those entities are satisfied with their business relationship with Trxade, if our buying group pharmacies and several of our vendors decided no longer to do business with us, that vendor void would materially and adversely affect our competitiveness in the marketplace.
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This is due to the fact that the SCN-102 (oral liquid) and the reference product are two different dosage forms. SCN-102 is an oral liquid formulation and therefore it is expected to have an earlier Cmax than the immediate release tablet.
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We depend on suppliers to make their drugs and other medical products available to us for resale and are subject to risks associated with the availability of these drugs and other medical products.
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Based on the discussion above, we believe that the impact of this Cmax difference will be minimal. ● The data obtained in the study is similar to the PK study data for the immediate release tablet. 8 Table of Contents If approved, SCN-102 would be the first FDA approved oral liquid formulation of losartan on the market.
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We do not directly manufacture any of the products we sell and instead we rely on third parties to manufacture and/or procure such drugs and other medical products for us to resell. Supply chain constraints have, and may in the future have, a negative impact on the availability of drugs and medical products that we sell.
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Scienture LLC submitted an Investigational New Drug (“IND”) application to the FDA in September 2022. Multiple human pharmacokinetics studies were performed, showing close comparability with the oral solid dosage form. In October 2023, Scienture LLC submitted an NDA for losartan potassium oral suspension to the FDA.
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Our supplier relationships could be interrupted, become less favorable to us or be terminated and the supply of these drugs or products could be interrupted or become insufficient.
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In December 2023, the FDA accepted the NDA for review and assigned a Prescription Drug User Fee Act (“PDUFA”) target action date of August 19, 2024.
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Supply interruptions or other disruptions in manufacturing processes could be caused by events beyond our control, including natural disasters, supplier facility shut-downs, defective raw materials, the impact of epidemics or pandemics, such as COVID-19, and actions by U.S. or international governments, including export restrictions or tariffs.
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Despite responding during the FDA’s review to information requests related to chemistry, manufacturing, and controls (“CMC”), pharmacovigilance, clinical, microbiology and labeling, the FDA issued a Complete Response Letter to Scienture LLC focused on the CMC information submitted. Scienture LLC prepared the requested information and resubmitted the NDA to the FDA on September 17, 2024.
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A sustained supply reduction or interruption, and an inability to develop alternative and additional sources for such supply, could result in lost sales, increased cost, damage to our reputation, and may have an adverse effect on our business. 25 We may have difficulties in sourcing or selling products due to a variety of causes.
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In October 2024, the FDA accepted the resubmitted NDA for review and assigned a PDUFA target action date of March 17, 2025.
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We might experience difficulties and delays in sourcing and selling products due to a variety of causes, such as: difficulties in complying with the legal requirements for export or import of pharmaceuticals or supplies; suppliers’ failure to satisfy production demand; manufacturing or supply problems such as inadequate resources; and real or perceived quality issues.
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On March 13, 2025, the FDA approved the SCN-102 NDA to be launched as ARBLI TM (losartan potassium) Oral Suspension, 10mg/mL Scienture LLC anticipates that it will commercially launch and bring to market SCN-102 during the third quarter of 2025. SCN-102 will be the first FDA approved oral liquid formulation of losartan on the market.
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Difficulties in product manufacturing or access to raw materials could result in supplier production shutdowns, product shortages and other supply disruptions. Any of these risks might have a materially adverse impact on our business operations and our financial position or results of operations. Rapid technological change in our industry presents us with significant risks and challenges .
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SCN-104 (Multi-dose Dihydroergotamine Mesylate (“DHE”) injection pen) The SCN-104 injection pen is a disposable, multiple fixed dose, single entity combination product comprised of a small molecule drug, SCN-104, which is administered using a customized injection pen. SCN-104 is a drug product containing DHE as the active ingredient.

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Item 1A. Risk Factors

Risk Factors — what could go wrong, per management

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Biggest changeThe doubt regarding our potential ability to continue as a going concern may adversely affect our ability to obtain new financing on reasonable terms or at all. Additionally, if we are unable to continue as a going concern, our stockholders may lose some or all of their investment in the Company.
Biggest changeThe doubt regarding our potential ability to continue as a going concern may adversely affect our ability to obtain new financing on reasonable terms or at all.
For example: a) We had $725,973 of loss on impairment of goodwill for the fiscal year ended December 31, 2020, in connection with the acquisition of Community Specialty Pharmacy, LLC; b) We designed and invested resources into the “Bonum Health Hub”, a self-enclosed, free standing virtual examination room, which was launched by the Company’s wholly-owned Bonum Health, LLC, in November 2019 and was expected to be operational in April 2020; however, the Company does not anticipate installations moving forward, and took a write off of the hubs purchased at June 30, 2021 in the amount of $143,891, which was included under loss on inventory investments in the statement of operations for the year ended December 31, 2021; c) We also used resources and funding to create a Health Passport application during 2020 and 2021, which was planned to store a user’s health and vaccination status and allow confirmation thereof via a QR code; however, we did not generate any revenue from this product and the product was discontinued at the end of December 2021; d) We had $792,500 of loss on impairment of intangible assets related to our investment in the joint venture SOSRx, LLC formed in February of 2022.
For example: a) We had $725,973 of loss on impairment of goodwill for the fiscal year ended December 31, 2020, in connection with the acquisition of Community Specialty Pharmacy, LLC; b) We designed and invested resources into the “Bonum Health Hub”, a self-enclosed, free standing virtual examination room, which was launched by the Company’s wholly-owned Bonum Health, LLC, in November 2019 and was expected to be operational in April 2020; however, the Company does not anticipate installations moving forward, and took a write off of the hubs purchased at June 30, 2021 in the amount of $143,891, which was included under loss on inventory investments in the statement of operations for the year ended December 31, 2021; 42 Table of Contents c) We also used resources and funding to create a Health Passport application during 2020 and 2021, which was planned to store a user’s health and vaccination status and allow confirmation thereof via a QR code; however, we did not generate any revenue from this product and the product was discontinued at the end of December 2021; d) We had $792,500 of loss on impairment of intangible assets related to our investment in the joint venture SOSRx, LLC formed in February of 2022.
These matters, when considered in the aggregate, raise substantial doubt about the Company’s ability to continue as a going concern for a reasonable period of time, which is defined as within one year after the date that our condensed financial statements are issued.
These matters, when considered in the aggregate, raise substantial doubt about our ability to continue as a going concern for a reasonable period of time, which is defined as within one year after the date that our condensed financial statements are issued.
The inventory was written down and was recorded as loss on inventory investment in the statement of operations during the year ended December 31, 2022; and d) During the year ended December 31, 2023 we acquired Superlatus through a merger transaction, however, due to various complications with the post-closing integration we elected to divest Superlatus in March 2024.
The inventory was written down and was recorded as loss on inventory investment in the statement of operations during the year ended December 31, 2022; and d) During the year ended December 31, 2023 we acquired Superlatus through a merger transaction, however, due to various complications with the post-closing integration we elected to divest Superlatus in March 2024 for $1.
You should carefully consider these risk factors before you decide to invest in our common stock. The reader should not consider this list to be a complete statement of all risks and uncertainties.
You should carefully consider these risk factors before you decide to invest in our common stock and should not consider this list to be a complete statement of all risks and uncertainties.
ITEM 1A. RISK FACTORS Summary Risk Factors Our business is subject to numerous risks and uncertainties, many of which are beyond our control, including those highlighted in the section titled “Risk Factors” immediately following this summary.
ITEM 1A. RISK FACTORS Summary Risk Factors Our business is subject to numerous risks and uncertainties, many of which are beyond our control, including those highlighted in the section titled Risk Factors immediately following this summary.
The financial statements incorporated by reference herein do not contain any adjustments to reflect the possible future effects on the classification of assets or the amounts and classification of liabilities that might result from the outcome of this uncertainty.
The financial herein do not contain any adjustments to reflect the possible future effects on the classification of assets or the amounts and classification of liabilities that might result from the outcome of this uncertainty.
We have invested and expect to continue to invest in new businesses, products, services, and technologies.
Our acquisitions and investments in new businesses and new products, services, and technologies is inherently risky, and could disrupt our ongoing businesses. We have invested and expect to continue to invest in new businesses, products, services, and technologies.
If we are unable to access additional capital moving forward, it may hurt our ability to grow and to generate future revenues, our financial position, and liquidity.
If we are unable to access additional capital moving forward, it may hurt our ability to grow and to generate future revenues, our financial position, and liquidity. Furthermore, we could be forced to delay, limit, reduce or terminate product development programs, future commercialization efforts or other operations.
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These risks include, among others, the following: ● We are currently unprofitable, have generated net losses, and we may incur losses in the future; ● We may need additional financing in the future, which may not be available on favorable terms, if at all; ● We may not be able to manage our future growth; ● Risks relating to implementing our acquisition strategies, and the risk that acquisitions will likely be dilutive to our stockholders and we may not realize the anticipated benefits of certain strategic transactions that we pursue or effect; ● Many of our competitors are better established and have resources significantly greater than ours; ● We face risks associated with our operations within the pharmaceutical distribution market; ● We are dependent on our current management; ● We rely on third party contracts, which may not be renewed or may be terminated; ● We may in the future face difficulties in sourcing products and inventory due to a variety of causes; ● We have in the past, and may in the future, not be able to sell our inventory, at or above the price we acquired such inventory for, have in the past, and may in the future, be forced to write-down inventory and certain of our other assets which may have a material adverse effect on our balance sheet; ● We have in the past, and may in the future, not receive products or receive refunds for deposited amounts and have experienced losses in connection with such deposits; ● We may be subject to claims that we violated intellectual property rights of others, which are extremely costly to defend and could require us to pay significant damages and limit our ability to operate; ● Our business and operations depend on the proper functioning of information systems, critical facilities and distribution networks and a disruption, cyber-attack, failure or destruction of such networks, systems, or technologies may disrupt our business or result in liability; ● There may be losses or unauthorized access to or releases of confidential information, including personally identifiable information, that could subject the Company to significant reputational, financial, legal and operational consequences; ● We face numerous risks, including risks associated with legal challenges, relationships with third parties and affiliated professionals, competition for services; new technologies, failure to develop widespread brand awareness and regulatory risks from the Office of Inspector General, U.S.
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These risks include, among others, the following: Risks Related to Our Business ● We operate a clinical-stage biopharmaceutical company with a limited operating history, which may make it difficult to evaluate its current business and predict its future success and viability. ● Our executive officers lack experience with the clinical development of therapeutic products for FDA marketing approval. ● We need additional capital which may not be available when needed or on commercially acceptable terms, thereby casting substantial doubt on our ability to continue as a going concern.
Removed
Department of Health and Human Services (OIG) and the United States Department of Justice (DOJ) and state regulators around pharmaceutical distribution now and in the future. ● Our certificate of incorporation limits the liability of our officers and directors and provides for indemnification rights, mandatory forum selection provisions and limits the ability of stockholders to call special meetings of stockholders; ● We incur significant costs to ensure compliance with U.S. and NASDAQ Capital Market reporting and corporate governance requirements; ● At various times we have not been in compliance with NASDAQ’s continued listing requirements, and may not be able to maintain the listing of our common stock on the NASDAQ Capital Market; ● Regulatory changes that affect our distribution channels could harm our business; ● Healthcare fraud laws are often vague and uncertain, exposing us to potential liability; ● New and expanded laws or regulations could have a material adverse effect on our business operations, cash flows or future prospects; ● The public health crisis involving the abuse of prescription opioid pain medication could have a material negative effect on our business operations and timely reporting to new state regulations. ● Consolidation in the U.S. healthcare industry may negatively impact our results of operations; ● We have identified material weaknesses in our internal control over financial reporting and controls and procedures; ● There may not be sufficient liquidity in the market for our securities in order for investors to sell their shares.
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Raising additional capital may cause dilution to our stockholders, restrict our operations or require us to relinquish rights to our product candidates.
Removed
The market price of our common stock may continue to be volatile; ● Stockholders may experience dilution to future equity sales, the exercise or conversion of outstanding convertible securities or future transactions; ● Our results of operations are subject to rising inflation, rising interest rates, governmental responses thereto and possible recessions caused thereby; ● Our Chief Executive Officer and President are our two largest stockholders and, as a result, they can exert significant control over us and have actual or potential interests that may differ from yours; ● Cyber security attacks and website problems; ● There is substantial doubt regarding our ability to continue as a going concern; and ● Claims, litigation, government investigations, and other proceedings that may adversely affect our business and results of operations. 17 Risk Factors You should be aware that there are substantial risks for an investment in our common stock.
Added
To the extent outstanding loan conversion rights associated with our existing indebtedness are exercised, there will be dilution to our stockholders. ● Indebtedness and liabilities could limit the cash flow available for our operations, including under Scienture LLC’s outstanding secured convertible debt, expose us to risks that could adversely affect our business, financial condition, and results of operations. ● Due to the significant resources required to develop our product pipeline, and depending on our ability to access capital, we must prioritize the development of certain product candidates over others and we may fail to expend our limited resources on product candidates or indications that may have been more profitable or for which there is a greater likelihood of success. ● Our acquisitions and investments in new businesses and new products, services, and technologies is inherently risky, and could disrupt our ongoing businesses. ● Our business is highly dependent on the success of certain product candidates.
Removed
Risks Related to Our Liquidity and Business Operations and Plans Our business, financial condition and results of operations are subject to various risks and uncertainties, including those described below. This section discusses factors that, individually or in aggregate, could cause our actual results to differ materially from expected and historical results.
Added
If we are unable to successfully complete clinical development, obtain regulatory approval for or commercialize one or more of our product candidates, or if we experience delays in doing so, our business will be materially harmed. ● We are dependent upon our current management, who may have conflicts of interest.
Removed
Our business, financial condition or results of operations could be materially adversely affected by any of these risks. It is not possible to predict or identify all such factors. Consequently, the following description of Risk Factors is not a complete discussion of all potential risks or uncertainties applicable to our business.
Added
Our ability to develop product candidates and our future growth depends on attracting, hiring and retaining key personnel and recruiting additional qualified personnel. ● We may seek to collaborate with third parties and may not be able to implement these collaborations on commercially acceptable terms, if at all.
Removed
We were recently unprofitable, we have recently generated net losses, and we may incur losses in the future. Revenues generated from our consolidated operations for the years ended December 31, 2023 and 2022 were $8,272,214 and $10,250,168, respectively.
Added
The success of certain of our product candidates may depend in significant part on the success of such collaborations. ● Our third-party manufacturing partners may be unable to increase the scale of production or product yield of our product candidates, resulting in increased manufacturing costs and delays in commercialization of our products.
Removed
We incurred a net loss of $13,720,546 for during the year ended December 31, 2023, compared to a net loss of $2,403,442 for the year ended December 31, 2022. We may incur other losses in the foreseeable future due to the significant costs associated with our business operations, including costs associated with maintaining industry regulatory and licensure compliance.
Added
Furthermore, changes in methods of manufacturing our product candidates could result in additional costs or delays. ● Our growth depends in part on the success of our strategic relationships with third parties.
Removed
We also incur significant compliance costs associated with maintaining SEC regulatory and financial reporting requirements; as well as costs to maintain minimum listing requirements of Nasdaq. We cannot assure you that our operations will annually generate sufficient revenues to fund our continuing operations or to fully implement our business plan, and thereafter sustain profitability in any future period.
Added
Some of these third parties may be located outside of the United States. ● Changes in methods of product candidate manufacturing or formulation may result in additional costs or delay. ● We may be subject to lawsuits. ● The successful development of Scienture LLC’s pharmaceutical products involves a lengthy and expensive process and is highly uncertain.
Removed
The likelihood of our success must be considered in light of the problems, expenses, difficulties, complications and delays frequently encountered in connection with the start and growth of a business, the implementation and execution of our business plan, and the regulatory environment affecting the distribution of pharmaceuticals in which we operate.
Added
Risks Related to Our Legal and Regulatory Requirements ● We are subject, directly or indirectly, to federal and state healthcare, fraud, abuse false claims, and other laws and regulations as well as health data privacy and security laws and regulations, contractual obligations and self-regulatory schemes.
Removed
We need additional capital which may not be available on commercially acceptable terms, if at all, which creates substantial doubt about our ability to continue as a going concern. Our historical financial statements have been prepared under the assumption that we will continue as a going concern. As of December 31, 2023, the Company had an accumulated deficit of $33,245,940.
Added
If we are unable to comply, or have not fully complied, with such laws, we could face investigations and substantial penalties. Furthermore, it may be difficult and costly for us to comply with the extensive government regulations to which our business is subject. ● We may be unable to obtain regulatory approval for our product candidates under applicable regulatory requirements.
Removed
We have limited financial resources, as of December 31, 2023, we had a working capital deficit of approximately $8,803,000 and a cash balance of approximately $152,000. We will need to raise additional capital or secure debt funding to support on-going operations.
Added
The denial or delay of any such approval would delay commercialization of our product candidates and adversely impact our business and results of operations. ● Even if we obtain regulatory approval for any of our product candidates, we will be subject to ongoing regulatory requirements, which may result in significant additional expenses.
Removed
The sources of this capital are expected to be the sale of equity and debt, which may not be available on favorable terms, if at all, and may, if sold, cause significant dilution to existing stockholders.
Added
Additionally, our product candidates, if approved, could be subject to labeling and other restrictions, and we may be subject to penalties if we fail to comply with regulatory requirements or experience unanticipated problems with our product candidates. 36 Table of Contents ● We intend to use certain regulatory pathways to seek regulatory approval of several of our product candidates.
Removed
Additional financing may not be available to us when needed or, if available, it may not be obtained on commercially reasonable terms.
Added
If the FDA concludes that our marketing applications no longer qualify for these regulatory pathways, then our applications may not be accepted by the FDA for review and approval of our products may be delayed. ● We may seek priority review designation for our product candidates.
Removed
If we are not able to obtain the necessary additional financing on a timely or commercially reasonable basis, we will be forced to delay or scale down some or all of our development activities (or perhaps even cease the operation of our business).
Added
We might not receive such designation, and even if we do, such designation may not lead to faster regulatory review or approval. ● We may seek orphan drug designation from the FDA for our product candidates.
Removed
Our access to additional capital may be negatively affected by future recessions, downturns in the economy or the markets as a whole, or inflation. 18 If we do not obtain additional financing, our business, prospects, financial condition and results of operations will be adversely affected.
Added
We may be unable to obtain such designation or, if obtained, to maintain the benefits associated with orphan drug status, including the potential for non-patent market exclusivity. ● If regulatory authorities approve generic versions of our products, or do not grant our products a sufficient period of market exclusivity before approving a generic version, our ability to generate revenue may be adversely affected. ● Even if we obtain FDA approval for a product candidate in the United States, we may never obtain approval for or successfully commercialize that candidate outside of the United States, which would limit our ability to realize a product’s full market potential. ● Even if we are able to commercialize any of our product candidates, the third-party payor coverage and reimbursement status of newly-approved products are uncertain.
Removed
Management anticipates that we will require additional working capital in the future to pursue continued development of products, services, and marketing operations. We cannot accurately predict the timing and amount of such capital requirements. Additional financing may not be available to us when needed or, if available, it may not be obtained on commercially reasonable terms.
Added
Failure to obtain or maintain adequate coverage and reimbursement for our product candidates could limit our ability to market those products and decrease our ability to generate revenue. ● We are developing a drug-device combination product, which may result in additional regulatory risks. ● Our third party collaborators and service providers are, or may become, subject to a variety of stringent and evolving privacy and data security laws, regulations, and rules, contractual obligations, industry standards, policies and other obligations related to privacy and data security.
Removed
If we are not able to obtain the necessary additional financing on a timely or commercially reasonable basis, we will be forced to delay or scale down some or all of our development activities (or perhaps even cease the operation of our business).
Added
Any actual or perceived failure to comply with such obligations could expose us to significant fines or other penalties and otherwise harm our business and operations. ● The FDA and other regulatory agencies actively enforce the laws and regulations prohibiting the promotion of off-label uses. ● Healthcare legislative reform measures may have a negative impact on our business and results of operations. ● Inadequate funding for the FDA and other government agencies, including from government shutdowns, or other disruptions to these agencies’ operations, could hinder such agencies’ ability to hire and retain key leadership and other personnel, prevent new products and services from being developed or commercialized in a timely manner or otherwise prevent those agencies from performing normal business functions on which the operation of our business may rely.
Removed
Our access to additional capital may be negatively affected by future recessions, downturns in the economy or the markets as a whole, or inflation. We have no commitments for any additional financing, and such commitments may not be obtained on favorable terms, if at all.
Added
Risks Related to Our Technology and Intellectual Property ● We may not be able to protect our intellectual property and trade secret rights throughout the world. If our efforts to protect our intellectual property rights are inadequate, we may not be able to compete effectively in our market. ● We depend on in-licensed intellectual property.
Removed
Any additional equity financing will be dilutive to our stockholders, and debt financing, if available, may involve restrictive covenants with respect to dividends, raising future capital, and other financial and operational matters.
Added
If we fail to comply with our obligations under intellectual property licenses with third parties, we could lose license rights that are important to our business. ● If we or our licensors are unable to obtain and maintain patent protection for our product candidates, or if the scope of the patent protection obtained is not sufficiently broad, our competitors could develop and commercialize products similar or identical to our product candidates, and our ability to successfully commercialize our product candidates may be adversely affected.
Removed
If we are unable to obtain additional financing as needed, we may be required to reduce the scope of our operations or our anticipated expansion, which could have a material adverse effect on us.
Added
Furthermore, we do not intend to seek patent protection for one of our products, SCN-106. ● Obtaining and maintaining patent protection depends on compliance with various procedural, document submission, fee payment and other requirements imposed by governmental patent agencies.
Removed
We have attempted to expand, and may further explore, the expansion of our business beyond our legacy healthcare and pharmacy focused business model, and those efforts may not prove successful. We expect to attempt to broaden our current assets and operations through additional business combinations and acquisition transactions.
Added
Our patent protection could be reduced or eliminated for non-compliance with these requirements. ● Issued patents covering our product candidates could be found invalid or unenforceable if challenged in court or the USPTO. ● Changes to patent law in the United States and in foreign jurisdictions could diminish the value of our patents in general, thereby impairing our ability to protect our product candidates. ● If we do not obtain patent term extension for our current product candidates, our business may be materially harmed. ● We may become involved in lawsuits to protect or enforce our intellectual property rights, which could be distracting, expensive, time consuming, and unsuccessful. 37 Table of Contents ● We may be subject to claims challenging the inventorship or ownership of our intellectual property or asserting that we violated intellectual property rights of others, the outcome of which would be uncertain.
Removed
Certain of these transactions may involve companies involved in industries that are outside and different from our legacy operations, which focused on the healthcare and pharmaceutical industries. For example, during the year ended December 31, 2023 we acquired Superlatus a diversified food technology company.
Added
These claims could be extremely costly to defend, could require us to pay significant damages and limit our ability to operate, and could distract our personnel from normal responsibilities. ● European patents and patent applications could be challenged in the recently created Unified Patent Court for the European Union. ● Our use, or the use by our third party collaborators and service providers, of new and evolving technologies, such as artificial intelligence (“AI”) and machine learning (“ML”), may result in spending additional resources and present new risks and challenges that can impact our business, including by posing security and other risks to our sensitive data.
Removed
These transactions, if successful, may result in a change of the Company’s focus, a change in the composition of its management, and otherwise result in the Company entering new businesses in which it does not have substantial prior experience.
Added
As a result, we may be exposed to reputational harm, other adverse consequences, and liability. ● If our trademarks and trade names are not adequately protected then we may not be able to build name recognition in our markets of interest and our business may be adversely affected.
Removed
As a result, these transactions may not prove successful or may result potential negative effects that prevent us from realizing the benefits of such transaction and, in turn, have a material adverse impact on our stock price, financial condition, results of operations and liquidity.
Added
Risks Related to Our Common Stock ● We may not be able to comply with Nasdaq’s continued listing standards. ● Our common stock has in the past been a “penny stock” under SEC rules, and may be subject to the “penny stock” rules in the future.
Removed
It is likely that any efforts we may make to acquire a business will result in substantial additional dilution to our stockholders. Our existing resources will likely be insufficient to support business operations for a significant period of time.
Added
It may be more difficult to resell securities classified as “penny stock.” ● The exercise of outstanding warrants, options and other securities that are exercisable into shares of our common stock will be dilutive to our existing stockholders. ● We have not historically paid or declared any dividends on our common stock and do not expect to pay or declare cash dividends in the future on a regular basis, if at all. ● Our common stock price is likely to be highly volatile because of several factors, including a limited public float. ● There may not be sufficient liquidity in the market for our securities in order for investors to sell their shares.
Removed
Furthermore, with any business combination or acquisition in which we engage, we will likely issue shares of our common stock rather than paying cash for the business.
Added
The market price of our common stock may continue to be volatile. ● Stockholders may be diluted significantly through our efforts to obtain financing and satisfy obligations through the issuance of additional shares of our common stock. Risk Factors You should be aware that there are substantial risks for an investment in our common stock.
Removed
Moreover, if we raise capital for any operations in the future or issue stock for a business combination or acquisition, such action will require the issuance of equity or debt securities which will likely result in substantial dilution to our existing stockholders.
Added
Risks Related to Our Business We operate a clinical-stage biopharmaceutical company with a limited operating history, which may make it difficult to evaluate its current business and predict its future success and viability. We hold a clinical-stage biopharmaceutical company with a limited operating history.
Removed
Although we will attempt to minimize the dilutive impact of any future business acquisition or capital-raising activities, we cannot offer any assurance that we will be able to do so. 19 Our acquisitions and investments in new businesses and new products, services, and technologies is inherently risky, and could disrupt our ongoing businesses.
Added
Scienture LLC was formed in 2019 and its operations to date have been limited to organizing and staffing its company, business planning, raising capital, identifying and developing its product candidates for the treatment of central nervous system (“CNS”) and cardiovascular (“CVS”) diseases, securing intellectual property rights, and planning and undertaking preclinical studies and clinical trials.
Removed
Failure to adequately manage our planned aggressive growth strategy may harm our business or increase our risk of failure. For the foreseeable future, we intend to pursue an aggressive growth strategy for the expansion of our operations through increased product development and marketing (or acquisitions of business operations and assets outside of our legacy operations).
Added
Scienture LLC has not yet demonstrated an ability to generate revenues, obtain regulatory approvals, manufacture any product on a commercial scale or arrange for a third party to do so on its behalf or conduct sales and marketing activities necessary for successful product commercialization.
Removed
Our ability to rapidly expand our operations will depend upon many factors, including our ability to work in a regulated environment, market value-added products effectively to independent pharmacies, establish and maintain strategic relationships with suppliers, and obtain adequate capital resources on acceptable terms.
Added
Scienture LLC’s limited operating history as a company makes any assessment of its future success and viability subject to significant uncertainty. Scienture LLC will encounter risks and difficulties frequently experienced by early-stage biopharmaceutical companies in rapidly evolving fields, and Scienture LLC has not yet demonstrated an ability to successfully overcome such risks and difficulties.
Removed
Any restrictions on our ability to expand may have a materially adverse effect on our business, results of operations, and financial condition. Accordingly, we may be unable to achieve our targets for sales growth, and our operations may not be successful or achieve anticipated operating results.
Added
If Scienture LLC does not address these risks and difficulties successfully, its business will suffer. 38 Table of Contents The success of our business depends primarily upon its ability to identify, develop, and commercialize product candidates, including our existing product candidates: SCN-102, SCN-104, SCN-106, and SCN-107.
Removed
Additionally, our growth may place a significant strain on our managerial, administrative, operational, and financial resources and our infrastructure. Our future success will depend, in part, upon the ability of our senior management to manage growth effectively.
Added
We only have one product candidate, SCN-102, for which it has conducted pivotal clinical studies to date, and we will be required to similarly perform pivotal clinical studies for the other products in its pipeline in order to obtain regulatory approval for these earlier stage candidates.
Removed
This will require us to, among other things: ● implement additional management information systems; ● further develop our operating, administrative, legal, financial, and accounting systems and controls; ● hire additional personnel; ● develop additional levels of management within our company; ● locate additional office space; ● maintain close coordination among our engineering, operations, legal, finance, sales and marketing, and client service and support organizations; and ● manage our expanding international operations. 20 As a result, we may lack the resources to deploy our services on a timely and cost-effective basis.
Added
Our business depends heavily on its ability to obtain FDA approval for SCN-102 and successfully launch this product candidate and do the same for the other products in its pipeline. We do not know whether it will be able to develop any products of commercial value.
Removed
Failure to accomplish any of these requirements could impair our ability to deliver services in a timely fashion or attract and retain new customers. Future business combinations and acquisition transactions, if any, as well as recently closed business combinations and acquisition transactions, may not succeed in generating the intended benefits and may adversely affect our business.
Added
We do not have any products approved for commercial sale and have not generated any revenue from product sales to date. We will continue to incur significant research and development and other expenses related to its preclinical and clinical development and ongoing operations. As a result, we are not profitable and has incurred losses in each period since its inception.
Removed
Part of our growth strategy is to evaluate strategic acquisitions or relationships from time to time. The inability of our management to successfully integrate acquired businesses, assets or technologies, and any related diversion of management’s attention, could have a material adverse effect on our business, operating results and financial condition.
Added
Net losses and negative cash flows have had, and likely will continue to have, an adverse effect on our financial condition. We expect to continue to incur significant losses for the foreseeable future, and we expect these losses to increase as we continue our research and development of, and seek regulatory approvals for, our product candidates.
Removed
Business combinations and other acquisition transactions may have a direct adverse effect on our financial condition, results of operations, liquidity or stock price.

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Item 1C. Cybersecurity

Cybersecurity — threats and controls disclosure

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Biggest changeDuring the year ended December 31, 2023, we did not identify any cybersecurity threats that have materially affected or are reasonably likely to materially affect our business strategy, results of operations, or financial condition.
Biggest changeAs of the date of this Annual Report on Form 10-K, we have no t experienced any significant cybersecurity attacks and, to date, the risks from cybersecurity threats have not materially affected, or are reasonably likely to materially affect, our business strategy, results of operations, or financial condition.
Removed
ITEM 1C. CYBERSECURITY The Company has not adopted any formal cybersecurity risk management program or formal processes for assessing, identifying, and managing material risks from cybersecurity threats. The full board of directors has oversight responsibility for the Company’s overall risk management, including cybersecurity risk, and has not delegated oversight authority for cybersecurity risks to any committee.
Added
ITEM 1C. CYBERSECURITY We maintain a cyber-risk management program which is intended to assist in assessing, identifying, and managing material risks from cybersecurity threats to our data and information systems. This program is to ensure that cybersecurity considerations are included in decision-making processes throughout the Company.
Added
Our approach consists of, among other things, cybersecurity threat and vulnerability prevention, detection, mitigation and remediation of potential cybersecurity risks. We employ cybersecurity intrusion detection systems and continuous monitoring, in order to help defend against unauthorized access. We also employ identity-based access controls and identity authentication requirements.
Added
Access to the Company’s data is monitored and controlled according to access control policies. Data protection and privacy practices, including data loss prevention, help to safeguard sensitive information.
Added
We have also outsourced significant elements of our information technology infrastructure; as a result, we manage independent vendor relationships with third parties who are responsible for maintaining significant elements of our information technology systems and infrastructure.
Added
Our Board of Directors is responsible for oversight of our cyber-risk management program and management’s role is to assist the Board of Directors in identifying and considering material cybersecurity risks, ensure implementation of management and employee level cybersecurity practices and training and provide the Board of Directors with regular reports regarding any cybersecurity attacks or vulnerabilities.
Added
For more information regarding the risks the Company faces from cybersecurity threats, see “Item 1A. Risk Factors––Risks Related to Our Business and Operations––We are increasingly dependent on information technology, and our systems and infrastructure face certain risks, including cybersecurity and data leakage risks.”

Item 2. Properties

Properties — owned and leased real estate

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Biggest changeWe believe our current and future facilities are adequate for our current and near-term needs. Additional space may be required as we expand our activities. We do not currently foresee any significant difficulties in obtaining any required additional facilities. 44
Biggest changeWe do not currently foresee any significant difficulties in obtaining any required additional facilities.
We entered into a lease for Integra Pharma Solutions, LLC at 6308 Benjamin Road, Tampa, Florida 33634 for approximately $43,000 per year ($3,583 per month) under a five-year lease agreement, effective October 17, 2018, occupying approximately 6,300 square feet.
ITEM 2. PROPERTIES We do not own any real property. We entered into a lease for Integra Pharma Solutions, LLC at 6308 Benjamin Road, Tampa, Florida 33634 for approximately $43,000 per year ($3,583 per month) under a five-year lease agreement, effective October 17, 2018, occupying approximately 6,300 square feet.
Removed
ITEM 2. PROPERTIES We do not own any real property. We entered into a lease for our current corporate office space at 2420 Brunello Trace, Lutz, Florida 33558 on November 8, 2021. The lease included a five-year term, beginning January 1, 2022, and ending December 31, 2026. The office space occupies approximately 9,850 square feet.
Added
Scienture LLC entered into a lease at 20 Austin Boulevard, Commack, NY 11725 for approximately $29,621 per year ($2,468 per month) under a 22-month agreement, effective October 1, 2023. We believe our current and future facilities are adequate for our current and near-term needs. Additional space may be required as we expand our activities.
Removed
Pursuant to the lease, the Company is responsible for water/sewer costs ($140 per month) and its proportionate share of the building’s operating expenses, including property taxes. We paid a security deposit of $38,500 in connection with our entry into the agreement, which was surrendered upon termination of the lease in November 2023.
Removed
We entered into a lease for Superlatus Food Service Holding Company, LLC at 20 Sarine Road, Wurtsboro, New York 12790 for approximately $132,000 per year ($11,000 per month) under a three-year lease agreement, effective October 1, 2023. As a result of our divestiture of Superlatus in March 2024 we no longer have obligations related to this lease.

Item 3. Legal Proceedings

Legal Proceedings — active lawsuits and investigations

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Biggest changeFor a description of our material pending legal proceedings, please see “Note 16 Contingencies”. to the Notes to Consolidated Financial Statements included herein under “Item 8. Financial Statements and Supplemental Data.” ITEM 4. MINE SAFETY DISCLOSURES Not applicable. PART II
Biggest changeFor a description of our material pending legal proceedings, please see “Note 15 Contingencies”. to the Notes to Consolidated Financial Statements included herein under “Item 8. Financial Statements and Supplemental Data.”

Item 5. Market for Registrant's Common Equity

Market for Common Equity — stock, dividends, buybacks

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Biggest changeITEM 5. MARKET FOR THE REGISTRANT’S COMMON EQUITY, RELATED STOCKHOLDER MATTERS AND ISSUER PURCHASES OF EQUITY SECURITIES Market for Common Stock Our common stock was approved for listing on The NASDAQ Capital Market under the symbol MEDS ”, on February 13, 2020. Prior to that, it traded on the OTCQB Market under the symbol TRXD ”.
Biggest changeITEM 5. MARKET FOR THE REGISTRANT’S COMMON EQUITY, RELATED STOCKHOLDER MATTERS AND ISSUER PURCHASES OF EQUITY SECURITIES Market for Common Stock Our common stock was approved for listing on Nasdaq on February 13, 2020, under the symbol “MEDS”. On September 24, 2024, in connection with our acquisition of Scienture, Inc. (k/n/a Scienture, LLC), we changed our symbol to “SCNX”.
Dividend Policy Although we paid a special cash dividend in the first quarter of 2024, we have not historically paid or declared any cash dividends on our common stock. Any determination to pay dividends in the future will be at the discretion of our board of directors.
Dividend Policy Although we paid a special cash dividend in the first and third quarters of 2024, we have not historically paid or declared any cash dividends on our common stock. Any determination to pay dividends in the future will be at the discretion of our board of directors.
Accordingly, investors have historically relied on sales of their common stock after price appreciation, which may never occur, as the only way to realize any future gains on their investments.
Accordingly, investors have historically relied on sales of their common stock after price appreciation, which may never occur, as the only way to realize any future gains on their investments. Recent Sales of Unregistered Securities During the year ended December 31, 2024, the Company issued 490,698 shares of common stock for services.
Common Stock and Preferred Stock Outstanding and Holders of Record As of April 22, 2024, we had 1,406,348 shares of common stock outstanding, held by 52 stockholders of record, not including holders who hold their shares in street name, and also shares of Series C Preferred Stock issued or outstanding.
Common Stock and Preferred Stock Outstanding and Holders of Record As of March 26, 2025, we had 12,515,019 shares of common stock outstanding, held by 90 stockholders of record, not including holders who hold their shares in street name as well as 1,575,900 shares of preferred stock issued and outstanding.
At present, there is a limited market for our common stock.
Prior to February 13, 2020, our common stock traded on the OTCQB Market under the symbol “TRXD”. At present, there is a limited market for our common stock.
Removed
Recent Sales of Unregistered Securities There were no sales of unregistered securities during the three months ended December 31, 2023, and from the period from January 1, 2024, to the filing date of this report, that were not previously disclosed in a Quarterly Report on Form 10-Q or in a Current Report on Form 8-K.
Added
The Company relied on the exemption from registration set forth in Section 4(a)(2) of the Securities Act for this issuance. On July 12, 2024, the Company converted 290 shares of Series C Preferred Stock into 52,158 shares of common stock at the election of the holder.
Removed
Issuer Purchases of Equity Securities In May and December of 2021, the Company’s Board of Directors authorized the repurchase of up to $1 million of the currently outstanding shares of the Company’s common stock.
Added
The Company relied on the exemption from registration set forth in Section 4(a)(2) of the Securities Act for this issuance.
Removed
Under the stock repurchase program, shares may be repurchased from time to time in the open market or through negotiated transactions at prevailing market rates, or by other means in accordance with federal securities laws.
Added
On July 25, 2024, as consideration for the acquisition of Scienture LLC, the Company issued to former Scienture, Inc. stockholders an aggregate amount of (i) 291,536 shares of the Company’s common stock and (ii) 6,826,713 shares of the Company’s Series X Non-Voting Convertible Preferred Stock, par value $0.00001 per share (the “Series X Preferred Stock”), each share of which was convertible into one share of common stock.
Removed
Repurchases will be made at management’s discretion at prices management considers to be attractive and in the best interests of both the Company and its stockholders, subject to the availability of stock, general market conditions, the trading price of the stock, alternative uses for capital, and the Company’s financial performance.
Added
On September 20, 2024, all shares of Series X Preferred Stock were converted into a total of 6,826,753 shares of common stock. Such issuances were made in reliance on the exemptions from registration pursuant to Section 4(a)(2) of the Securities Act.
Removed
Any open market purchases will be conducted in accordance with the limitations set forth in Rule 10b-18 of Exchange Act and other applicable legal requirements. Repurchases may also be made under a Rule 10b5-1 plan.
Added
In August 2024, the Company issued a convertible note of $360,000, for which the Company received $314,000 in net proceeds. The Conversion Price is the lesser of i) $8.36 or (ii) 85% of the lowest volume-weighted average prices of the preceding five trading days. The note matures on August 20, 2025.
Removed
There was no time frame or expiration date for the repurchase program, and such program was to remain in place until a maximum of $1.0 million of the Company’s common stock had been repurchased or until such program was suspended or discontinued by the Board of Directors.
Added
In connection with the note, the Company issued 76,923 warrants to purchase common stock. The warrants have an exercise price of $9.36 per share, are immediately exercisable and have a term of 5 years.
Removed
During Fiscal 2023 the Company did not repurchase or any shares of the Company’s common stock under the repurchase program. 45
Added
Such issuances were made in reliance on the exemptions from registration pursuant to Section 4(a)(2) of the Securities Act. 75 Table of Contents Also in August 2024, the Company issued 28,571 shares of common stock pursuant to the exercise of warrants on a cashless basis.
Added
Such issuances were made in reliance on the exemptions from registration pursuant to Section 4(a)(2) of the Securities Act. On November 22, 2024, the Company issued 55,000 shares of common stock pursuant to a Securities Purchase Agreement dated November 22, 2024.
Added
On November 25, 2024, the Company issued 70,000 shares of common stock pursuant to purchase agreement dated November 25, 2024. Such issuances were made in reliance on the exemptions from registration pursuant to Section 4(a)(2) of the Securities Act.
Added
In each case, the issuance did not involve a public offering and was made without general solicitation or general advertising, and the recipient of the shares was an accredited investor. Purchases of Equity Securities by the Issuer and Affiliated Purchasers The Company did not repurchase any shares of common stock during the year ended December 31, 2024.

Item 7. Management's Discussion & Analysis

Management's Discussion & Analysis (MD&A) — revenue / margin commentary

27 edited+49 added77 removed3 unchanged
Biggest changeLiquidity Cash, current assets, current liabilities, short term debt and working capital at the end of each period were as follows: December 31, 2023 December 31, 2022 Cash $ 151,908 $ 1,094,894 Current assets (excluding cash) 2,601,154 998,229 Current liabilities (excluding short term debt) 5,026,355 1,980,124 Short term debt 6,530,000 166,667 Working deficit (8,803,293 ) (53,668 ) Our principal sources of liquidity during the years ended December 31, 2023 and 2022 have been cash provided by operations (internal source).
Biggest changeLiquidity Cash, current assets, current liabilities, short term debt and working capital at the end of each period were as follows: December 31, Percent 2024 2023 Change Change Cash $ 308,096 $ 314 $ 307,782 98020 % Current assets (excluding cash) $ 5,997,381 $ 2,752,749 $ 3,244,632 118 % Current liabilities $ 7,906,893 $ 11,556,355 $ (3,649,462 ) -32 % Working capital $ (1,601,416 ) $ (8,803,292 ) $ 7,201,876 -82 % Our principal sources of liquidity have historically been cash provided by operations, sales of business assets and operations from time to time, sales of equity, and borrowings under various debt arrangements.
Critical Accounting Policies and Estimates Our discussion and analysis of our financial condition and results of operations are based upon our consolidated financial statements, which have been prepared in accordance with accounting principles generally accepted in the United States of America.
Critical Accounting Policies Our discussion and analysis of our financial condition and results of operations are based upon our consolidated financial statements, which have been prepared in accordance with accounting principles generally accepted in the United States of America.
The preparation of these financial statements requires us to make estimates and judgments that affect the reported amounts of assets and liabilities and disclosure of contingent assets and liabilities at the date of the financial statements and the reported amounts of net sales and expenses for each period.
The preparation of these financial statements requires us to make estimates and judgments that affect the reported amounts of assets and liabilities and disclosure of contingent assets and liabilities at the date of the financial statements and the reported amount of net sales and expenses for each period.
As a consequence, actual results may differ materially from those in the forward-looking statements. See “Item 1A. Risk Factors” of this report for the discussion of risk factors. For all periods presented, the consolidated statements of income and consolidated balance sheet data have been adjusted for the reclassification of discontinued operations information, unless otherwise noted.
As a consequence, actual results may differ materially from those in the forward-looking statements. See Item 1A. Risk Factors of this Annual Report for the discussion of risk factors. For all periods presented, the consolidated statements of income and consolidated balance sheet data have been adjusted for the reclassification of discontinued operations information, unless otherwise noted.
Our plan for the next twelve months is to continue using the same marketing and management strategies to promote our Integra Pharma Solutions assets and operations, exploring strategic transactions involving our corporate assets, while also seeking to expand our operations organically or through acquisitions, as funding and opportunities arise.
Our plan for the next twelve months is to continue using the same marketing and management strategies to promote our IPS assets and operations, exploring strategic transactions involving our corporate assets, while also seeking to expand our and Scienture LLC operations organically or through acquisitions, as funding and opportunities arise.
This discussion contains forward-looking statements based on the views and beliefs of our management, as well as assumptions and estimates made by our management. See “Cautionary Statement Regarding Forward-Looking Information” above. These statements by their nature are subject to risks and uncertainties and are influenced by various factors.
This discussion contains forward-looking statements based on the views and beliefs of our management, as well as assumptions and estimates made by our management. See the section entitled Cautionary Statement Regarding Forward-Looking Information above. These statements by their nature are subject to risks and uncertainties and are influenced by various factors.
ITEM 7. MANAGEMENT’S DISCUSSION AND ANALYSIS OF FINANCIAL CONDITION AND RESULTS OF OPERATIONS The following discussion of the Company’s historical performance and financial condition should be read together with the consolidated financial statements and related notes in “Item 8. Financial Statements and Supplemental Data” of this Report.
ITEM 7. MANAGEMENT’S DISCUSSION AND ANALYSIS OF FINANCIAL CONDITION AND RESULTS OF OPERATIONS The following discussion of the Company’s historical performance and financial condition should be read together with the consolidated financial statements and related notes in the section entitled Item 8. Financial Statements and Supplemental Data of this Annual Report.
We expect that our future available capital resources will consist primarily of cash generated from operations, remaining cash balances, proceeds from potential asset divestitures or strategic transactions, borrowings, and any additional funds raised through sales of debt and/or equity.
We expect that our future available capital resources will consist primarily of cash generated from operations, remaining cash balances, borrowings, and additional funds raised through sales of debt and/or equity securities.
An analysis of our financial results comparing the years ended December 31, 2023, and 2022. Liquidity and Capital Resources . An analysis of changes in our balance sheets and cash flows and discussion of our financial condition. Critical Accounting Policies and Estimates .
An analysis of changes in our consolidated balance sheets and cash flows and discussion of our financial condition. Results of Operations . An analysis of our financial results comparing the years ended December 31, 2024, and 2023. Critical Accounting Policies .
All references to years relate to the calendar year ended December 31 of the particular year. Our Management’s Discussion and Analysis of Financial Condition and Results of Operations (the MD&A ”) is provided in addition to the accompanying consolidated financial statements and notes to assist readers in understanding our results of operations, financial condition, and cash flows.
Summary of The Information Contained in Management’s Discussion and Analysis of Financial Condition and Results of Operations Our Management’s Discussion and Analysis of Financial Condition and Results of Operations (MD&A) is provided in addition to the accompanying consolidated financial statements and notes to assist readers in understanding our results of operations, financial condition, and cash flows.
Accounting policies and estimates that we believe are important to understanding the assumptions and judgments incorporated in our reported financial results and forecasts. Recently Issued Accounting Standards . A summary of recently issued accounting standards affecting the Company, if any.
Accounting estimates that we believe are important to understanding the assumptions and judgments incorporated in our reported financial results and forecasts.
We may require additional funding in the future to expand or complete acquisitions. The sources of this capital are expected to be equity investments and notes payable. Our plan for the next twelve months is to continue development of the information technology used in the Company subsidiaries.
We may require additional funding in the future to implement on our business plan and potentially to expand or complete acquisitions. The sources of this capital are expected to be equity investments and notes payable.
We estimate our operating expenses and working capital requirements for the next 12 months to be approximately as follows: Projected Expenses for 2024 Amount General and administrative (1) $ 4,800,000 Total $ 4,800,000 (1) Includes wages and payroll, legal and accounting, marketing, rent and technology development. We may require additional funding in the future to expand or complete acquisitions.
We may also raise additional funding in the future through the sale of equity. 77 Table of Contents We estimate our operating expenses and working capital requirements for the next 12 months to be approximately as follows: Projected Expenses from January 2025 to December 2025 Amount General and administrative (1) $ 9,800,000 Total $ 9,800,000 (1) Includes estimated wages and payroll, legal and accounting, marketing, rent and research and development.
We will require additional funding, we may seek to raise that through the sale of debt or equity, which may not be available on favorable terms, if at all, and may, if sold, cause significant dilution to existing stockholders.
The sources of this capital are expected to be the sale of equity and debt, which may not be available on favorable terms, if at all, and may, if sold, cause significant dilution to existing stockholders.
Our principal uses of cash have been for operating expenses and research and development of our newer business units. We anticipate these uses will continue to be our principal uses of cash in the future in addition to any necessary business acquisitions. We currently do not have any material unused sources of liquid assets.
Our principal uses of cash have been for operating expenses, technology development, and acquisitions. We anticipate these uses will continue to be our principal sources of, and uses of, cash in the future.
Stock option forfeitures are recognized at the date of employee termination. Effective January 1, 2019, the Company adopted ASU 2018-07 for the accounting of share-based payments granted to non-employees for goods and services.
Stock option forfeitures are recognized at the date of employee termination. Effective January 1, 2019, the Company adopted ASU 2018-07 for the accounting of share-based payments granted to non-employees for goods and services. Off-Balance Sheet Arrangements During the periods presented, we did not have, nor do we currently have, any off-balance sheet arrangements as defined under SEC rules.
Stock-Based Compensation We account for stock-based compensation to employees in accordance with ASC 718, Compensation-Stock Compensation ”.
Stock-Based Compensation The Company accounts for stock-based compensation to employees in accordance with ASC 718, “Compensation-Stock Compensation”.
Recently Issued Accounting Standards For more information on recently issued accounting standards, see Note 2 - Summary of Significant Accounting Policies , to the Notes to Consolidated Financial Statements included herein under Item 8. Financial Statements and Supplemental Data ”.
Recently Issued Accounting Standards For more information on recently issued accounting standards, see “NOTE 1 ORGANIZATION AND BASIS OF PRESENTATION”, to the Notes to Consolidated Financial Statements included herein under “PART I. - ITEM 1. FINANCIAL STATEMENTS”.
(4) The Urgent Company, Inc., our wholly-owned subsidiary, is a retail and distribution provider of prepackaged, prepared foods. Subsequent to December 31, 2023, we divested our interest in The Urgent Company, LLC.
The Urgent Company, Inc., which was a wholly-owned subsidiary, is a retail and distribution provider of prepackaged, prepared foods.
If we are unable to access additional capital moving forward, it may hurt our ability to grow and to generate future revenues. We believe that we have adequate cash to implement our plan to operate a business-to-business web-based marketplace focused on the United States pharmaceutical industry.
If we are unable to access additional capital moving forward, it may hurt our ability to grow and to generate future revenues.
Cash used in investing activities for the year ended December 31, 2023 was $275,717. This compared to $427,845 of cash used in investing activities for the year ended December 31, 2022. In 2023, the net cash used mainly related to net cash exchanged in acquisition and disposals.
Cash provided by investing activities for the year ended December 31, 2024, was $27,552,791 and cash used in investing activities was $275,717 for the year ended December 31, 2023.
Gross profit as a percentage of sales was 31.4% for the year ended December 31, 2023, compared to 53.8% for the year ended December 31, 2022. The reason for the decrease in gross profit as a percentage of sales was a result of increased inventory and cost of sales associated with The Urgent Company.
Gross profit as a percentage of sales was 4.39% for the year ended December 31, 2024, compared to 3.60% for the year ended December 31, 2023. Wages and salary expense increased by $1,484,520 for the year ended December 31, 2024 to $2,111,067 compared to $626,547 for the comparable period in 2023.
Net loss from operations increased $11,317,104 to a net loss of $13,720,546 for the year ended December 31, 2023, compared to a net loss of $2,403,442 for the year ended December 31, 2022.
Net income from discontinued operations increased by $36,670,988 to a net income of $27,310,278 for the year ended December 31, 2024, compared to a net loss from discontinued operations of $9,360,710 for the year ended December 31, 2023.
During the year ended December 31, 2022, the cash was used for an investment in capitalized software for Delivmeds. Cash provided by financing activities for the year ended December 31, 2023 was $1,406,332 and cash used in financing activities for the year ended December 31, 2022, was $35,171.
Cash provided by in financing activities for the year ended December 31, 2024, was ($14,979,770) compared to $1,406,332 of cash provided by financing activities for the year ended December 31, 2023. The change was primarily due to the payment of dividends of $14,858,831 in 2024.
Results of Operations For the Year Ended December 31, 2023, compared to the Year Ended December 31, 2022 The following selected consolidated financial data should be read in conjunction with the consolidated financial statements and the notes to these statements included in “Item 8. Financial Statements and Supplemental Data” of this Report.
In August 2024, the Company received note proceeds of $314,000 and $2,640,000 in net proceeds from convertible debenture in November 2024. Results of Operations The following selected consolidated financial data should be read in conjunction with the unaudited consolidated financial statements and the notes to these statements included above.
The Company takes orders for products, creates invoices for each order and recognizes revenue at the time the Customer receives the product. Customer returns, to date, have not been material. (3) Community Specialty Pharmacy, LLC, our wholly-owned subsidiary, is a licensed retail pharmacy.
IPS takes orders for products, creates invoices for each order and recognizes revenue at the time the product is shipped to the Customer. Customer returns are not material. Step One: Identify the contract with the Customer IPS requires that an application and a credit card for payment be completed by the Customer prior to the first order.
General and administrative expenses (less stock-based compensation expense) increased for the year ended December 31, 2023 to $2,498,123 compared to $1,355,946 for the year ended December 31, 2022. The increase is largely driven by amortization expense related to intangible assets acquired through the Sapientia Technologies acquisition.
The increase is primarily due to increase in amount of legal services during the year ended December 31, 2024 as compared to the same period in 2023. General and administrative expenses (including stock-based compensation expense) increased by $5,369,446 for the year ended December 31, 2024, to $6,706,082 compared to $1,336,637 for the comparable period in 2023.
Removed
MD&A is organized as follows: ● Plan of Operations . Summary of the Company’s plan of operations for the next 12 months. ● Sources of Revenue . Summary of the main sources of Company revenue during the reported periods. ● Results of Operations .
Added
All references to years relate to the calendar year ended December 31 of the particular year.
Removed
Plan of Operations We had a working capital deficit of $8,803,293 as of December 31, 2023, compared to working capital deficit of $53,668 as of December 31, 2022. The decrease in working capital of $8,749,625 is related to decreases in cash and increases in liabilities.
Added
MD&A is organized as follows: ● Company Overview . Discussion of our business and overall analysis of financial and other highlights affecting us, to provide context for the remainder of MD&A. ● Recent Events . Summary of material transactions occurring during year ended December 31, 2024. ● Liquidity and Capital Resources .
Removed
Below are reasons for the decrease in working capital. ● Cash decreased approximately $943,000 from December 31, 2022 to December 31, 2023.
Added
Company Overview On September 20, 2024, the Company filed with the Secretary of State of the State of Delaware an amendment to its Second Amended and Restated Certificate of Incorporation to change the legal name of the Company from “TRxADE HEALTH, Inc.” to “Scienture Holdings, Inc.” The Company owned, as of December 31, 2024, 100% of Softell Inc.
Removed
The reasons for the decrease are as follows: ○ $250,000 repayments of debt, net of new debt issuances; and ○ $733,694 paid for interest expense related to the sale of future accounts receivable. ● Increases in current liabilities of approximately $9,409,564 from December 31, 2022 to December 31, 2023 were driven by the following main factors: ○ $1,554,070 increase in accounts payable balance as of December 31, 2023 compared to the comparable period; ○ $1,138,310 increase in the balance due on the sale of future accounts receivable as of December 31, 2023 compared to the comparable period; ○ $6,363,333 increase in the current portion of notes payable balance; and a ○ $350,000 increase in purchase price payable balance as of December 31, 2023 compared to the comparable period.
Added
(f/k/a Trxade Inc.), Integra Pharma Solutions, LLC and Scienture, LLC (f/k/a Scienture, Inc.). 76 Table of Contents On October 4, 2024, the Company and Softell entered into IPS Assignment Agreement, pursuant to which the Company transferred, and Softell accepted, 100% of the membership interests of IPS. As a result, IPS is now a wholly-owned subsidiary of Softell.
Removed
With our current cash on hand, expected revenues, and based on our current average monthly expenses, we anticipate the need for additional funding in order to continue our operations at their current levels, and to pay the costs associated with being a public company, for the next 12 months.
Added
During the year ended December 31, 2023 and a portion of the quarter ended March 31, 2024, Softell, operated a web-based market platform that enabled commerce among healthcare buyers and sellers of pharmaceuticals, accessories and services. Softell’s current primary operations are conducted through IPS. IPS is a licensed pharmaceutical wholesaler and sells brand, generic and non-drug products to customers.
Removed
As our business continues to grow, customer feedback will be integral in making small adjustments to improve the product and overall customer experience.
Added
IPS’ customers include all healthcare markets including government organizations, hospitals, clinics and independent pharmacies nationwide. Bonum Health, LLC was formed to hold certain telehealth assets acquired in October 2019. The “Bonum Health Hub” was launched in February 2020; however, the Company does not anticipate installations moving forward.
Removed
If we are unable to access additional capital moving forward, it may hurt our ability to grow and to generate future revenues. 46 Sources of Revenue During 2023 we had four main revenue streams: (1) Trxade, Inc., our wholly-owned subsidiary, provides an online web-based buying and selling platform for licensed pharmaceutical wholesalers (“ Suppliers ”) to sell products and services to licensed pharmacies (“ Customers ”).
Added
The Company is in the process of determining a divestment and winddown plan for Softell and IPS. On January 25, 2025, the Company’s Board of Directors approved the preparation of a divestment and winddown plan for the winddown of each of Softell, IPS, Bonum Health, Inc., and Bonum.
Removed
The Company charges Suppliers a transaction fee, a percentage of the purchase price of the prescription drugs and other products sold through its website service. The Company holds no inventory and assumes no responsibility for the shipment or delivery of any products or services from our website.
Added
Scienture LLC is a New York based branded, specialty pharmaceutical research company which is engaged in the research and development of branded pharmaceutical products. The intellectual property application process was initiated in November 2019 and the product development activities commenced in January 2020.
Removed
The Company considers itself an agent for this revenue stream and as such, reports revenue as net. Subsequent to December 31, 2023, we divested substantially all of our assets previously owned and operated by Trxade, Inc. (2) Integra Pharma Solutions, LLC, our wholly-owned subsidiary, is a licensed wholesaler of brand, generic and non-drug products to Customers.
Added
Scienture LLC also plans to foray into commercialization of innovative and branded pharmaceutical products in the US market. Scienture LLC’s assets in development are across therapeutics areas and indications and cater to different market segments. Scienture LLC’s mission is to identify, develop and bring to market innovative technology-based products to address unmet medical needs.
Removed
The Company fills prescriptions for drugs written by a doctor and recognizes revenue at the time the patient confirms delivery of the prescription. Customer returns, to date, have not been material. In August 2023 we sold our entire interest in Community Specialty Pharmacy, LLC.
Added
Its targeted portfolio consists of short term and long-term opportunities with efficient development, regulatory, and go to market strategies.
Removed
For all years presented, the consolidated statements of income and consolidated balance sheet data set forth in this Form 10-K have been adjusted for the reclassification of discontinued operations information, unless otherwise noted.
Added
Acquisitions See ITEM 1 of PART 1 Dispositions See ITEM 1 of PART 1 Recent Events On September 20, 2024, the Company filed with the Secretary of State of the State of Delaware an amendment to its Second Amended and Restated Certificate of Incorporation to change the legal name of the Company from “TRxADE HEALTH, Inc.” to “Scienture Holdings, Inc.” (the “Name Change”).
Removed
Fiscal Year Ended December 31, Percentage 2023 2022 Change Change Revenues $ 8,272,214 $ 10,250,168 (1,977,954 ) (19.3 %) Cost of sales 5,673,957 4,730,897 943,060 19.9 % Gross profit 2,598,257 5,519,271 (2,921,014 ) (52.9 %) Operating expenses: Loss on inventory investment - 875,250 (875,250 ) (100 %) Technology, research & development 1,376,908 993,185 383,723 38.6 % Wages and salary 2,698,178 3,581,089 (882,911 ) (24.7 %) Accounting and legal 1,534,377 829,751 704,626 84.9 % Professional fees 1,466,567 466,735 999,832 214.2 % Other general and administrative (less stock-based compensation expense) 2,498,123 1,355,946 1,142,177 84.2 % Warrants and options expense 287,510 333,284 (45,774 ) (13.7 %) Total operating expenses 9,861,663 8,435,240 1,426,423 16.9 % Change in fair value of warrant liability (148,420 ) 825,544 (973,964 ) (118.0 %) Interest, net (1,194,148 ) (315,217 ) (878,931 ) 278.8 % Goodwill impairment (5,129,115 ) - (5,129,115 ) (100.0 %) Gain on disposal of asset - 2,200 (2,200 ) (100.0 %) Other income 14,543 - 14,543 100.0 % Net loss from operations $ (13,720,546 ) $ (2,403,442 ) $ (11,317,104 ) 470.9 % Loss on discontinued operations (4,123,028 ) (1,506,426 ) (2,616,602 ) 173.7 % Net loss attributable to TRxADE Health, Inc.
Added
Other than the Name Change, there were no changes to the Company’s certificate of incorporation or bylaws. Effective September 23, 2024, the Company’s common stock trades under the ticker symbol “SCNX”. The Name Change resulted in a change to the CUSIP number for the Company’s outstanding shares of common stock offered on the Nasdaq Stock Market LLC.
Removed
(17,843,574 ) (3,472,099 ) (14,371,475 ) 413.9 % Net loss attributable to non-controlling interests - (437,769 ) 437,769 (100.0 %) 47 Operations Our revenues during the years ended December 31, 2023, and 2022 were mainly from the Trxade Inc. platform, Integra Pharma Solutions, and The Urgent Company.
Added
Liquidity Outlook Cash Explanation Cash Requirements Our primary objectives for the year of 2025 are expected to be the continued implementation of the Scienture LLC business plan, and to complete potential strategic transactions of our business-to-consumer subsidiaries, which may include a potential sale, spin-off, fund raising, combination or other strategic transaction, and also include the winding down of such entities.
Removed
Revenues decreased $1,977,954 for fiscal year 2023, compared to the prior year’s revenue of $10,250,168. Trxade, Inc., revenue increased by $852,933 or 16% to $6,200,334, compared to $5,347,401, for the years ended December 31, 2023, and 2022, which is attributable to a 16% increase in sales volume on the platform in 2023.
Added
Going Concern The accompanying consolidated financial statements have been prepared assuming that the Company will continue as a going concern, which contemplates realization of assets and the satisfaction of liabilities in the normal course of business within one year after the date the consolidated financial statements are issued.
Removed
Integra Pharma Solutions’ revenue decreased by $3,390,237, or 71%, which is attributable to decreased sales volume and pricing changes. The Trxade, Inc. platform is a secondary marketplace for pharmaceuticals and medical supplies with consistent growth year over year.
Added
In accordance with Financial Accounting Standards Board, or the FASB, Accounting Standards Update No. 2014-15, Presentation of Financial Statements - Going Concern (Subtopic 205-40), our management evaluates whether there are conditions or events, considered in aggregate, that raise substantial doubt about our ability to continue as a going concern within one year after the date that the financial statements are issued.
Removed
Cost of sales was $5,673,957 and gross profit was $2,598,257, for the year ended December 31, 2023, compared to $4,730,897 and $5,519,271, respectively, for the year ended December 31, 2022. The increase in cost of sales is attributed to the inventory costs and inventory write-downs associated with The Urgent Company.
Added
As of December 31, 2024, the Company had an accumulated deficit of $39,038,973 and $308,096 in cash. We will need to raise additional capital or secure debt funding to support on-going operations, and to fund the assets and operations of any businesses or assets we acquire.
Removed
Technology, research and development expenditures increased to $1,376,908 for the year ended December 31, 2023, compared to $993,185 for the year ended December 31, 2022, as the Company continued to develop apps for customers and make improvements to our platform technology.
Added
If we are unable to access additional capital moving forward, it may hurt our ability to grow and to generate future revenues, our financial position, and liquidity. These factors raise substantial doubt about the ability of the Company to continue as a going concern.
Removed
Professional fees increased for the year ended December 31, 2023 by $999,832 to $1,466,567 compared to $466,735 for the year ended December 31, 2022. The increase in professional fees for the year ended December 31, 2023 related to the merger with Superlatus and purchase of The Urgent Company.
Added
Unless Management is able to obtain additional financing, it is unlikely that the Company will be able to meet its funding requirements during the next 12 months. The financial statements do not include any adjustments that might result from the outcome of this uncertainty.
Removed
Total stock-based compensation expense decreased by 13.7% or $45,774 to $287,510 from $333,284 for the year ended December 31, 2023, compared to the prior year’s period. The decrease was due to less common stock issued for services during the year ended December 31, 2023 compared to the year ended December 31, 2022.
Added
Cash Flows The following table summarizes our Consolidated Statements of Cash Flows for the following periods: Year Ended December 31, Percent 2024 2023 Change Change Net cash (used in) provided by operating activities from continuing operations (13,286,163 ) 3,645,257 (16,931,420 ) -464 % Net cash used in operating activities from discontinued operations (979,075 ) (5,870,449 ) 4,891,373 -83 % Operating Activities (14,265,238 ) (2,225,192 ) (12,040,046 ) 541 % Net cash used in investing activities from continuing operations (2,379,024 ) (344,454 ) (2,034,570 ) 591 % Net cash provided by investing activities from discontinued operations 29,931,815 68,737 29,863,078 43445 % Investing Activities 27,552,791 (275,717 ) 27,828,508 -10093 % Net cash (used in) provided by financing activities from continuing operations (12,974,770 ) 1,906,332 (14,881,102 ) -781 % Net cash used in financing activities from discontinued operations (5,000 ) (500,000 ) 495,000 -99 % Financing Activities (12,979,770 ) 1,406,332 (14,386,102 ) -1023 % Net change in cash $ 307,782 $ (1,094,577 ) $ 1,402,358 -128 % 78 Table of Contents Cash used in operating activities for the year ended December 31, 2024, was $14,265,238 compared to $2,225,192 in 2023.
Removed
The Company recognized a loss on inventory investment of $875,520 for the year ended December 31, 2022, in connection with COVID-19 test kits that were purchased and could not be resold due to issues with the FDA. 48 The Company had interest expense, net, of $1,194,148 for the year ended December 31, 2023, compared to interest expense of $315,217 for the year ended December 31, 2022.
Added
The increase in cash used in operations for the year ended December 31, 2024 was mainly due to our net loss and cash used in operating assets and liabilities in 2024 driven by other receivables, partially offset by non-cash charges.
Removed
The increased interest expense is driven by the increases in the contingent funding liability due to additional accounts receivable advances during the year ended December 31, 2023. During the year ended December 31, 2023, the Company recognized a loss from the change in the fair value of warrants of $148,420.
Added
The increase in cash provided by investing activities in 2024 was primarily due to the MMS disposition in the first quarter and cash received in acquisition of Scienture, Inc., partially offset by the investment in securities of $2,500,000.
Removed
During the year ended December 31, 2022, the Company recognized a gain from the change in the fair value of warrants of $825,544. The Company recognized a goodwill impairment loss of $5,129,115 for the year ended December 31, 2023.
Added
Year Ended December 31, 2024, compared to Year Ended December 31, 2023 Year Ended December 31, Percent 2024 2023 Change Change Revenues $ 136,643 1,363,830 (1,227,187 ) -90 % Cost of sales 130,638 1,314,800 (1,184,162 ) -90 % Gross profit 6,005 49,031 (43,026 ) -88 % Operating expenses: Wage and salary expense 2,111,066 626,547 1,484,519 237 % Professional fees 1,458,332 875,136 583,196 67 % Accounting and legal expense 1,807,041 1,506,881 300,160 20 % Technology expense 416,311 100,280 316,031 315 % General and administrative (including stock-based compensation expense) 6,677,580 1,336,637 5,340,943 400 % Research and development 2,236,690 - 2,236,690 100 % Total operating expenses 14,707,020 4,445,482 10,261,538 231 % Change in fair value of warrant liability (182,982 ) (148,420 ) (34,562 ) 23 % Change in fair value of derivative liability 180,383 - 180,383 100 % Investment impairment (2,500,000 ) - (2,500,000 ) -100 % Interest income 135,337 4,198 131,139 3124 % Loss on disposal of asset (374,968 ) (2,798,968 ) 2,424,000 -87 % Interest expense (1,335,631 ) (1,143,223 ) (192,408 ) 17 % Net loss from continuing operations (18,778,876 ) (8,482,864 ) (10,296,011 ) 121 % Benefit / (provision) for income taxes 534,396 - 534,396 100 % Net loss from continuing operations, net of tax (18,244,480 ) (8,482,864 ) (9,761,615 ) 87 % Income (loss) from discontinued operations, net of tax 27,310,278 (9,360,710 ) 36,670,988 -392 % Net income/(loss) $ 9,065,798 $ (17,843,574 ) $ 26,909,372 -151 % 79 Table of Contents There were $136,643 in revenues for the year ended December 31, 2024.
Removed
The goodwill resulted from the acquisition of Superlatus and was subsequently determined to be impaired based on the facts and circumstances surrounding the sale of Superlatus on March 5, 2024.
Added
Revenues decreased by $1,227,187, compared to the same period ended December 31, 2023 primarily because of the disposition of the assets and operations of Softell completed in February 2024 which resulted in the Company having fewer revenue generating operations when compared to the comparable period in 2023.
Removed
The increase in net loss is mainly due to the write-down of inventory due to spoilage, increases in spending related to the merger transaction with Superlatus and purchase of TUC and goodwill impairment charges.
Added
For the year ended December 31, 2024, cost of goods sold and gross profit were $130,638 and $6,005, and $1,314,800 and $49,031, all respectively for the same period in 2023.
Removed
Net loss from discontinued operations increased $2,616,602 to a net loss of $4,123,028 for the year ended December 31, 2023, compared to a net loss from discontinued operations of $1,506,426 for the year ended December 31, 2022. Liquidity and Capital Resources Cash and Cash Equivalents Cash and cash equivalents were $151,908 as of December 31, 2023.
Added
Cost of goods sold decreased by $1,184,162, compared to the same period ended December 31, 2023 primarily because of the disposition of the assets and operations of Softell completed in February 2024 which resulted in the Company having fewer cost of goods sold.
Removed
During the year ended December 31, 2023, sales of future receivables provided a principal source of liquidity. During the year ended December 31, 2022, equity capital and borrowings under various debt arrangements (external source) and a stock placement deal of 920,000 shares.
Added
The increase is primarily due to an increase in salary of the COO and CEO of IPS, as well as the increased personnel as a result of the Scienture Merger in July 2024, as compared to the same period in 2023. Professional fees increased by $583,196 to $1,458,332 compared to $875,136 for the comparable period in 2023.
Removed
Cash decreased by $942,986 and other current assets increased by $1,602,925. The decrease in cash was primarily due to interest expense associated with the sale of future receivables and net repayments of debt as well as the professional fees and accounting and legal expenses associated with the merger with Superlatus and the acquisition of The Urgent Company.

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Item 7A. Quantitative and Qualitative Disclosures About Market Risk

Market Risk — interest-rate, FX, commodity exposure

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Biggest changeITEM 7A. QUANTITATIVE AND QUALITATIVE DISCLOSURES ABOUT MARKET RISK Pursuant to Item 305(e) of Regulation S-K 229.305(e)), the Company is not required to provide the information required by this Item as it is a smaller reporting company, as defined by Rule 229.10(f)(1). 53
Biggest changeITEM 7A. QUANTITATIVE AND QUALITATIVE DISCLOSURES ABOUT MARKET RISK Pursuant to Item 305(e) of Regulation S-K 229.305(e)), the Company is not required to provide the information required by this Item as it is a smaller reporting company, as defined by Rule 229.10(f)(1). 82 Table of Contents ITEM 8.
Added
FINANCIAL STATEMENTS AND SUPPLEMENTAL DATA Scienture Holdings, Inc. formerly TRxADE HEALTH, INC.
Added
FORM 10-K For the Year Ended December 31, 2024 TABLE OF CONTENTS REPORT OF INDEPENDENT REGISTERED PUBLIC ACCOUNTING FIRM PCAOB ID: 6866 84 CONSOLIDATED BALANCE SHEETS 85 CONSOLIDATED STATEMENTS OF OPERATIONS 86 CONSOLIDATED STATEMENTS OF STOCKHOLDERS’ EQUITY 87 CONSOLIDATED STATEMENTS OF CASH FLOWS 88 NOTES TO CONSOLIDATED FINANCIAL STATEMENTS 89 83 Table of Contents PART II: FINANCIAL INFORMATION

Other SCNX 10-K year-over-year comparisons