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Revenue climbs but YD Bio (Nasdaq: YDES) posts $8.3M 2025 net loss

Filing Impact
(Neutral)
Filing Sentiment
(Neutral)
Form Type
6-K

Rhea-AI Filing Summary

YD Bio Limited reported full-year 2025 net revenue of $596,817, up 17% from 2024, driven mainly by higher pharmaceutical sales, including Keytruda and new product launches. Gross profit rose to $167,410, but the sales mix shifted toward lower-margin drugs and peripherals, pressuring margins.

Total operating expenses surged to $5.4 million from $1.6 million, reflecting higher professional fees, a $1.1 million increase in research and development tied to licensed patents and know‑how, and a $1.3 million rise in staff costs as the business expanded.

Net loss widened sharply to $8.3 million from $1.4 million, mainly due to a $3.2 million adverse change in fair value of warrant liabilities and higher operating costs. Cash and cash equivalents increased to $6.0 million from $3.1 million, supported by a $13.9 million equity raise. The company ended 2025 with warrant liabilities of $14.99 million and a shareholders’ equity deficit of $2.86 million.

Positive

  • Revenue growth and stronger liquidity: Net revenue rose 17% year over year to $596,817, led by higher pharmaceutical sales and new products, while cash and cash equivalents increased to $6.0 million from $3.1 million, supported by a $13.9 million equity raise.

Negative

  • Sharp increase in losses and equity deficit: Net loss widened to $8.3 million from $1.4 million, total operating expenses more than tripled to $5.4 million, warrant liabilities reached $14.99 million, and shareholders’ equity swung to a $2.86 million deficit.
  • Margin pressure from sales mix shift: A move from higher-margin medical products toward lower-margin drugs and medical peripherals caused cost of revenue to grow faster than revenue, limiting gross profit improvement despite higher sales.

Insights

Revenue grew, but higher spending and warrant revaluation drove a much larger loss and equity deficit.

YD Bio delivered 17% revenue growth to $596,817, helped by higher pharmaceutical volumes, especially Keytruda, and new launches. However, the product mix shifted toward lower-margin drugs and peripherals, so gross profit grew more slowly to $167,410.

Operating expenses climbed to $5.4 million, over triple the prior year, driven by consulting and expansion costs, a $1.1 million increase in R&D for licensed patents and know-how, and a $1.3 million rise in staff costs. These choices reflect an investment phase but significantly increase the cost base.

Net loss expanded to $8.3 million, with a $3.2 million negative change in fair value of warrant liabilities adding to the operating shortfall. The balance sheet now shows $6.0 million in cash but a shareholders’ equity deficit of about $2.86 million, largely due to the new $14.99 million warrant liability. Overall, the filing shows stronger liquidity but materially higher losses and leverage to warrant valuation.

Net revenue 2025 $596,817 Year ended December 31, 2025
Net revenue growth 17% 2025 vs 2024
Net loss 2025 $8,311,316 Year ended December 31, 2025
Total operating expenses $5,439,131 Year ended December 31, 2025
Cash and cash equivalents $6,007,615 As of December 31, 2025
Warrant liabilities $14,991,482 As of December 31, 2025
Shareholders’ equity (deficit) -$2,855,663 As of December 31, 2025
Basic and diluted EPS ($0.12) Year ended December 31, 2025
private investment in public equity (PIPE) financial
"alongside a $13.2 million private investment in public equity (PIPE) financing"
A private investment in public equity (PIPE) is when a publicly traded company sells new shares or instruments that can become shares directly to a small group of private investors instead of through the open market. Think of it like a company taking a private loan from a few investors rather than holding a big public sale; it raises cash fast but can dilute existing owners and signal either financial need or strong backing by informed investors.
Drug Master Files (DMFs) regulatory
"filing Drug Master Files (DMFs) with the U.S. Food and Drug Administration"
Drug master files (DMFs) are confidential submissions to health regulators that contain detailed technical information about how a drug ingredient or component is made, tested and controlled, allowing a manufacturer to share safety and quality data without exposing proprietary trade secrets. For investors, DMFs are a signal that a company’s supply chain and manufacturing practices are documented and inspectable, which can help speed approvals, reduce regulatory risk and protect product continuity—think of them as locked blueprints that reassure regulators and partners that a product can be produced reliably.
Investigational New Drug (IND) regulatory
"This paves the way for us to submit Investigational New Drug (IND) applications to the FDA"
An investigational new drug (IND) is a drug or biologic that is being tested but has not yet been approved for general use; it is the application and formal status that allows a company to begin human clinical trials under regulator oversight. Investors care because an IND marks the transition from lab work to human testing — like getting a permit to run real-world experiments — which creates important milestones, costs, timelines and regulatory risk that drive a development-stage company's value.
Breakthrough Device regulatory
"toward an FDA Q-Submission to discuss potential Breakthrough Device eligibility"
'Breakthrough device' is a regulatory designation for a medical device judged to offer a substantial improvement in diagnosing or treating a serious or life‑threatening condition, granting it priority review and more intensive interaction with regulators to accelerate approval. For investors, it matters because the label can shorten time to market and reduce regulatory uncertainty—like putting a product into the fast lane—potentially raising commercial value and lowering development risk.
LDT-first strategy medical
"operates DNA methylation–based oncology testing programs in the United States under an LDT-first strategy"
warrant liabilities financial
"Change in fair value of warrant liabilities | | | (3,168,091 | )"
Warrant liabilities are the financial obligations a company records when it grants warrants—special rights allowing someone to buy shares at a set price in the future. If the warrants are expected to be exercised, they are treated as a liability because the company might need to deliver shares or cash later. This matters to investors because it affects the company’s reported financial health and the potential dilution of existing shares.

 

 

UNITED STATES

SECURITIES AND EXCHANGE COMMISSION

WASHINGTON, D.C. 20549

 

 

 

FORM 6-K

 

 

 

REPORT OF FOREIGN PRIVATE ISSUER

PURSUANT TO RULE 13a-16 OR 15d-16

OF THE SECURITIES EXCHANGE ACT OF 1934

 

For the Month of April 2026

 

Commission File Number: 001-42810

 

 

 

YD Bio Limited

 

 

 

12F., No. 3, Xingnan St.,

Nangang Dist.,

Taipei City 115001, Taiwan

(Address of principal executive offices)

 

 

 

Indicate by check mark whether the registrant files or will file annual reports under cover of Form 20-F or Form 40-F.

 

Form 20-F ☒     Form 40-F ☐

 

 

 

 

 

Issuance of Press Release

 

On April 30, 2026, YD Bio Limited (the “Company”) issued a press release announcing the Company’s financial results for the year ended December 31, 2025. A copy of the press release is furnished as Exhibit 99.1 to this Report on Form 6-K (this “Report”) and is incorporated herein by reference.

 

The information contained in this Report is hereby incorporated by reference into the Company’s Registration Statement on Form S-8 (File No. 333-292554) to be a part thereof, to the extent not superseded by documents or reports subsequently filed or furnished. This Report, including Exhibit 99.1, shall not otherwise be deemed “filed” for purposes of Section 18 of the Securities Exchange Act of 1934 or otherwise subject to the liabilities of that section, nor shall it be deemed incorporated by reference into any other filing under the Securities Act of 1933 or the Securities Exchange Act of 1934, except as expressly set forth by specific reference in such filing.

 

Forward Looking Statements

 

Matters discussed in this Report may constitute forward-looking statements. Forward-looking statements include statements concerning plans, objectives, goals, strategies, future events or performance, and underlying assumptions and other statements, other than statements of historical facts. The words “aim”, “believe”, “may”, “intends”, “expect”, “outlook”, “pending”, “will” and similar expressions identify forward-looking statements. The forward-looking statements in this Report are based upon various assumptions. Although we believe that these assumptions were reasonable when made, because these assumptions are inherently subject to significant uncertainties and contingencies which are difficult or impossible to predict and are beyond our control, we cannot assure you that we will achieve or accomplish these expectations. Except as required by law, the Company disclaims any duty to update these forward-looking statements.

 

EXHIBIT INDEX

 

The following exhibits are being filed herewith:

 

Exhibit No.   Description
99.1   Press Release, dated April 30, 2026

 

1

 

 

SIGNATURES

 

Pursuant to the requirements of the Securities Exchange Act of 1934, the registrant has duly caused this report to be signed on its behalf by the undersigned, thereunto duly authorized.

 

April 30, 2026

 

  YD BIO LIMITED
   
  By: /s/ Edmund Hen
  Name:  Edmund Hen
  Title: Chief Financial Officer

 

 

 

 

Exhibit 99.1

 

YD Bio Limited Reports Full Year 2025 Financial Results

 

TAIPEI, Taiwan, April 30, 2026 (GLOBE NEWSWIRE) -- YD Bio Limited (“YD Bio” or the “Company”) (Nasdaq: YDES), a biotechnology company advancing DNA methylation-based cancer detection technology and ophthalmologic innovations, today announced its financial results for the full year ended December 31, 2025.

 

Management Commentary

 

“2025 was a highly transformative and foundational year for YD Bio, characterized by the successful capitalization of our long-term strategic vision. The successful completion of our business combination with Breeze Holdings Acquisition Corp. in August 2025, alongside a $13.2 million private investment in public equity (PIPE) financing, helped to significantly strengthen our balance sheet. Furthermore, we achieved a 17% increase in net revenue, driven predominantly by expanded pharmaceutical sales volumes and strategic new product launches,” said Dr. Ethan Shen, Chairman and CEO of YD Bio. “We ended the year well-capitalized with approximately $6.0 million in cash and cash equivalents, which we believe positions us to securely meet our operating obligations in 2026 and aggressively pursue our clinical milestones.”

 

“During the past year, we consciously increased our research and development expenditures by approximately $1.1 million to secure essential licensed patents and technological know-how, and we restructured our sales mix to rapidly scale our commercial footprint. These foundational investments in our clinical service infrastructure and diagnostics platform are designed to support robust growth across multiple regulated healthcare segments.”

 

“Looking ahead, our strategic focus for 2026 is to aggressively advance our proprietary assets from validation toward expanded regulatory and commercial execution. We have already achieved certain milestones in our therapeutics pipeline by completing comprehensive Chemistry, Manufacturing, and Controls (CMC) development and filing Drug Master Files (DMFs) with the U.S. Food and Drug Administration (FDA) for our Limbal Stem Cell (LSC) platform and derived exosome products. This paves the way for us to submit Investigational New Drug (IND) applications to the FDA for both Dry Eye Disease and Age-Related Macular Degeneration in 2026. Concurrently, we are advancing our OkaiDx™ Pancreatic Cancer Early Detection Program toward an FDA Q-Submission to discuss potential Breakthrough Device eligibility and building upon our EG Telehealth Platform, which was recently launched in March 2026 to support diagnostic service delivery across the United States.”

 

“Finally, our vision to become an integrated, multi-vertical healthcare platform is being aggressively pursued through strategic M&A activity. For example, the previously announced merger with EG BioMed aims to seamlessly integrate DNA methylation-driven artificial intelligence platforms into our oncology programs,” said Dr. Shen.

 

 

 

YD Bio’s Full Year 2025 Financial Results

 

Through the Company’s combined diagnostics platform, clinical service infrastructure, and healthcare commercialization capabilities, YD Bio seeks to develop a scalable operating model designed to support growth across multiple regulated healthcare segments. The following table presents selected summarized financial information taken from YD Bio’s consolidated statements of operations for the year ended December 31, 2025 and 2024.

 

In thousands USD, except percentage data, differences due to rounding   For the years ended December 31,  
    2025     2024     Variance %  
Net Revenue   $ 597       510       17 %
Cost of Revenue     (429 )     (355 )     21 %
Gross Profit     168       155       8 %
General and Administrative Expenses     3,663       1,125       226 %
Selling and Marketing Expenses     171       2       8,450 %
Research and Development Expenses     1,602       491       226 %
Impairment of expected credit loss     3       (1 )     400 %
Total Operating Expenses     5,439       1,617       236 %
Loss from Operations     (5,271 )     (1,462 )     261 %
Net Loss     (8,310 )     (1,412 )     489 %

 

Net Revenue

 

Net revenue increased by $86,457 or 17% to $596,817 for the year ended December 31, 2025, compared to $510,360 for the year ended December 31, 2024. The top 5 individual products by revenue accounted for 41% of the total revenue during the period. The increase in revenue was primarily due to higher sales volumes and a shift in product mix toward lower-priced products, as reflected in the decrease in average selling price. Pharmaceutical sales, particularly Keytruda, which increased by approximately $48,598 driven by higher purchase volumes from key customers, along with new product launches, were the primary growth drivers. This growth was partially offset by decreased medical product sales, primarily due to the discontinuation of certain products and reduced orders for PVA eye cleansing tablets as a key customer adjusted its procurement strategy based on end-market feedback. Overall, the revenue change reflects a structural shift from higher-priced medical products toward pharmaceuticals and other lower-priced offerings.

 

Top five individual products by revenue for the year ended December 31, 2025:

 

Product

  Revenue 
Keytruda Injection (Drugs)  $133,138 
HQ Revitalizing and Renewing Tencel Mask (Beauty Products)   36,749 
Exolens Hioxifilcon (Contact lenses)   35,000 
Mounjaro Pen (Drugs)   22,025 
12-Lead Electrocardiograph (Medical and related products)   20,416 
Subtotal  $247,328 

 

Top five individual products by revenue for the year ended December 31, 2024:

 

Product

  Revenue 
PVA Eye Cleansing Wipes (Medical and related products)  $97,512 
Keytruda injection (Drugs)   84,540 
Immune Defense Proteins (Nutritional products)   33,613 
Fluorescence Cell Counter and Viability Analyzer (Medical and related products)   23,177 
Faslodex solution for injection (Drugs)   21,127 
Subtotal  $259,969 

 

2

 

 

Cost of Revenue

 

Cost of revenue increased by $74,403 or 21% to $429,407 for the year ended December 31, 2025, compared to $355,004 for the year ended December 31, 2024. The cost of revenue consists primarily of purchase costs of products for resales. The increase in cost of revenue was higher than the increase of net revenue, which was primarily due to the change in sales mix to the products sold with a lower margin during the year. Specifically, the sales mix shifted from higher-margin medical products to drugs and medical peripherals with relatively lower margins, resulting in a decrease in overall gross margin. This impact was partially offset by lower procurement costs for certain products.

 

Gross Profit

 

Gross profit increased by $12,054 or 8% to $167,410 for the year ended December 31, 2025, compared to $155,356 for the year ended December 31, 2024. The year-to-year changes were primarily due to higher sales volumes and a shift in product mix toward lower-priced products.

 

Operating Expenses

 

For the year ended December 31, 2025, the Company’s total operating expenses were approximately $5.4 million, reflecting an increase of $3.8 million compared to $1.6 million for the year ended December 31, 2024. The increase was mainly caused by the increase in professional and consultancy service fees related to the Company’s expansion and restructuring costs of $1.1 million, the increase in research and development expenses by $1.1 million related to two licensed patents and know-how, and by the $1.3 million increase in staff costs from the expansion of the Company’s business.

 

Net Loss

 

As a result of the foregoing, net loss for the year ended December 31, 2025 was $8.3 million compared to $1.4 million for the year ended December 31, 2024. The increase in net loss was mainly caused by the increase of change in fair value of warrant liabilities by $3.2 million, professional and consultancy service fees related to the Company expansion and restructuring by $1.1 million, research and development expenses by $1.1 million related to two licensed patents and know-how, and by the $1.3 million increase in staff costs from the expansion of the Company’s business.

 

Cash and Cash Equivalents

 

As of December 31, 2025, YD Bio’s cash was $6.0 million compared to $3.1 million as of December 31, 2024. This increase was primarily due to an equity raise of $13.9 million, offset by deferred offering cost of approximately $3.2 million, professional and consultancy services fees related to the Company expansion and restructuring of $1.5 million, research and development expenses of $1.1 million, payment for purchase of medical products and contact lenses of $1.9 million and prepayment for the purchase of office space and parking facilities of $1.5 million.

 

YD Bio Major Developments and 2026 Outlook

 

Therapeutics and Limbal Stem Cell Platform

 

Completed comprehensive Chemistry, Manufacturing, and Controls development for the Limbal Stem Cell platform and its derived exosome products.

 

Filed Drug Master Files with the FDA for both Limbal Stem Cells and derived exosomes.

 

Planning to establish a clinical-grade Limbal Stem Cell bank and submit an Investigational New Drug application for Dry Eye Disease in 2026.

 

Expecting to complete preclinical, efficacy, and toxicity studies for Age-Related Macular Degeneration, followed by an Investigational New Drug submission in 2026.

 

3

 

 

Diagnostics and Telehealth

 

Operating the online EG Telehealth Platform offering CLIA- and CAP-certified laboratory services across 44 U.S. states, Washington D.C., and Guam.

 

Advancing the OkaiDx™ Pancreatic Cancer Early Detection Program through a clinical validation pathway aligned with the FDA.

 

Aiming to complete patient enrollment, data cleaning, quality control, and preliminary statistical analysis for the OkaiDx™ program in 2026.

 

Planning a Q-Submission to the FDA to discuss potential Breakthrough Device eligibility for the pancreatic cancer program.

 

Strategic Expansions and Acquisitions

 

Announced a non-binding Memorandum of Understanding on January 6, 2026, to merge with EG BioMed.

 

Announced a binding Letter of Intent on January 20, 2026, to acquire Safe Save Medical Cell Sciences & Technology Co., Ltd.

 

Announced a Master Strategic Alliance Agreement by and between YD Bio USA, Inc. and YC Biotech Co., Ltd. On February 25, 2026.

 

About YD Bio Limited

 

YD Bio is a U.S.-anchored public biotechnology company building an integrated healthcare platform across regulated diagnostics, clinical services, and commercial healthcare markets. The Company operates DNA methylation–based oncology testing programs in the United States under an LDT-first strategy and provides compliant life science distribution and clinical trial supply chain services to pharmaceutical and biotechnology partners. In addition, the Company maintains regulated ocular health commercialization operations and a consumer health distribution platform in Asia. Through strategic partnerships and scalable execution capabilities, the Company aims to advance biomedical innovation with real-world clinical and commercial impact. For more information, visit ir.ydesgroup.com and follow the Company on Facebook, X, Threads, Instagram and LinkedIn.

 

Forward-Looking Statements

 

This press release contains forward-looking statements, including, among others, statements about the Company’s strategy, ongoing transactions, and expected commercialization and regulatory timelines. Forward-looking statements are based on current expectations, estimates, forecasts, and projections and are not guarantees of future performance. Investors can identify these forward-looking statements by words or phrases such as “aim,” “target,” “approximates,” “believes,” “designed to,” “hopes,” “expects,” “anticipates,” “estimates,” “projects,” “intends,” “plans,” “will,” “would,” “should,” “could,” “may” or other similar expressions. Actual results may differ materially due to a variety of factors, including regulatory decisions and feedback, the ability to consummate certain transactions and achieve their anticipated benefits, and other risks and uncertainties described in YD Bio’s filings with the U.S. Securities and Exchange Commission (the “SEC”). The Company undertakes no obligation to update any forward-looking statements, except as required by law. The Company cautions investors that actual results may differ materially from the anticipated results and encourages investors to review other factors that may affect its future results in the Company’s Annual Report on Form 20-F, registration statement and other filings with the SEC.

 

For investor and media inquiries, please contact:

 

YD Bio Limited
Investor Relations
Email: investor@ydesgroup.com

 

WFS Investor Relations Inc.
Email: services@wfsir.com
Phone: +1 628 283 9214

 

4

 

 

YD BIO LIMITED
CONSOLIDATED BALANCE SHEETS

 

   As of
December 31,
2025
   As of
December 31,
2024
 
   US$   US$ 
ASSETS        
CURRENT ASSETS        
Cash and cash equivalents   6,007,615    3,132,298 
Accounts receivable, net   167,477    86,582 
Other receivables from an affiliate, net   291,540    16,927 
Inventories   1,879,542    37,335 
Prepaid expenses and other current assets   1,324,016    194,740 
TOTAL CURRENT ASSETS   9,670,190    3,467,882 
           
Operating lease right-of-use assets, net   8,470    23,698 
Property, plant and equipment, net   59,340    64,379 
Intangible assets   2,609,739    2,680,035 
Deferred offering costs   -    628,232 
Prepaid expenses, non-current   1,431,658    - 
TOTAL ASSETS   13,779,397    6,864,226 
           
LIABILITIES          
CURRENT LIABILITIES          
Due to affiliates   785,665    37,253 
Operating lease liabilities, current   6,764    16,581 
Accounts payable   413,290    26,866 
Accrued expenses and other liabilities   437,859    182,360 
TOTAL CURRENT LIABILITIES   1,643,578    263,060 
           
Deferred tax liabilities       1,463 
Operating lease liabilities, non-current       5,684 
Accrued expenses and other liabilities, non-current       3,773 
Warrant Liabilities   14,991,482     
TOTAL LIABILITIES   16,635,060    273,980 
           
Commitments and contingencies          
           
SHAREHOLDERS’ EQUITY (DEFICIT)          
Common shares ($0.0001 par value, 500,000,000 shares authorized; 70,789,261 and 64,730,411 issued and outstanding as of December 31, 2025 and 2024, respectively)*   7,079    6,473 
Additional paid-in capital*   7,161,681    8,465,744 
Accumulated deficits   (10,238,359)   (1,927,043)
Accumulated other comprehensive income   213,936    45,072 
Total shareholders’ equity (deficit)   (2,855,663)   6,590,246 
TOTAL LIABILITIES AND SHAREHOLDERS’ EQUITY (DEFICIT)   13,779,397    6,864,226 

 

5

 

 

YD BIO LIMITED
CONSOLIDATED STATEMENTS OF OPERATIONS
AND COMPREHENSIVE INCOME/(LOSS)

 

   Years ended December 31, 
   2025   2024   2023 
   US$   US$   US$ 
Revenue   596,817    510,360    350,131 
Cost of revenue   (429,407)   (355,004)   (196,686)
Gross profit   167,410    155,356    153,445 
                
Operating expenses               
General and administrative expenses   3,663,141    1,124,469    153,069 
Selling and marketing expenses   170,523    1,957    7,492 
Research and development expenses   1,602,064    491,353     
Impairment (Recovery) of expected credit loss   3,403    (493)   2,731 
Total operating expenses   5,439,131    1,617,286    163,292 
                
Loss from operations   (5,271,721)   (1,461,930)   (9,847)
                
Other income (expense)               
Other income, net   46,803    64,415    29,351 
Interest income   80,162    11,808    290 
Interest expenses       (772)   (2,144)
Change in fair value of warrant liabilities   (3,168,091)        
Total other income (expense), net   (3,041,126)   75,451    27,497 
                
(Loss) Income before income tax   (8,312,847)   (1,386,479)   17,650 
Income tax   1,531    (25,080)   (4,090)
Net (loss) income   (8,311,316)   (1,411,559)   13,560 
                
Other comprehensive (loss) income, net of tax:               
Change in foreign currency translation adjustments   168,864    (2,139)   99 
Other Comprehensive (loss) income   (8,142,452)   (1,413,698)   13,659 
                
Basic and diluted net (loss) income per share   (0.12)   (0.02)   0.0002 
Basic and diluted weighted average number of shares outstanding   66,719,177    64,730,411    64,730,411 

 

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FAQ

How did YD Bio (YDES) perform financially in 2025?

YD Bio reported 2025 net revenue of $596,817, a 17% increase over 2024. Gross profit reached $167,410, but higher operating expenses and warrant revaluation led to a net loss of $8,311,316, significantly larger than the prior year’s $1,411,559 loss.

What drove YD Bio’s revenue growth in 2025?

Revenue growth was mainly driven by higher pharmaceutical sales volumes and new product launches. Keytruda sales increased by about $48,598 due to higher purchases from key customers, while overall revenue mix shifted toward lower-priced pharmaceutical and related products versus higher-priced medical items.

Why did YD Bio’s net loss increase in 2025?

Net loss rose to $8.3 million primarily because total operating expenses climbed to $5.4 million and the change in fair value of warrant liabilities added $3.17 million in expense. Higher professional fees, staff costs, and R&D spending also contributed to the larger loss.

How much did YD Bio spend on research and development in 2025?

YD Bio’s research and development expenses were $1,602,064 in 2025, up from $491,353 in 2024. The increase of about $1.1 million was mainly related to securing two licensed patents and associated technological know-how to support its therapeutics and diagnostics platforms.

What is YD Bio’s cash position and capital structure after 2025?

As of December 31, 2025, YD Bio held $6,007,615 in cash and cash equivalents, up from $3,132,298. However, warrant liabilities totaled $14,991,482, and accumulated deficits reached $10,238,359, resulting in a shareholders’ equity deficit of $2,855,663 instead of prior positive equity.

How did operating expenses change for YD Bio in 2025?

Total operating expenses rose to $5,439,131 in 2025 from $1,617,286 in 2024. General and administrative expenses increased to $3,663,141, selling and marketing to $170,523, and research and development to $1,602,064, reflecting expansion, higher professional fees, and investment in licensed patents.

Filing Exhibits & Attachments

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