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Q1 2026: 20/20 BioLabs (AIDX) revenue declines as cash rises on $5M raise

Filing Impact
(Moderate)
Filing Sentiment
(Neutral)
Form Type
8-K

Rhea-AI Filing Summary

20/20 BioLabs reported first quarter 2026 results showing lower revenue and a wider loss but a much stronger cash position. Revenue for the three months ended March 31, 2026 was $353,375, down from $553,820 a year earlier, with gross margin at 17.8%.

Net loss widened to $2,174,836 from $764,577, reflecting higher sales, general and administrative costs tied to becoming a Nasdaq-listed public company, non-cash losses on convertible notes, and warrant remeasurement. Cash and cash equivalents increased to $4,219,099 from $1,025,987 at year-end, helped by a $5,000,000 Series E preferred stock private placement and new convertible notes.

The company highlighted state-funded firefighter cancer screening programs expected to drive revenue growth beginning in Q2 2026, a distribution agreement with Evexia Diagnostics, a CKD-focused license with ROKIT Healthcare, and the commercial launch of its OneTest™ for Longevity chronic disease risk test.

Positive

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Insights

Q1 shows revenue softness and higher losses, offset by stronger cash from new financing.

20/20 BioLabs generated Q1 2026 revenue of $353,375, down from $553,820, as firefighter program timing and seasonal patterns affected orders. Gross margin compressed to 17.8%, reflecting lower volume and product mix, while operating expenses rose to $1,506,240 as the company scaled public-company infrastructure.

Net loss increased to $2,174,836, driven by higher operating costs and non-cash items including a $322,359 loss on issuance of a convertible note and $148,766 from warrant revaluation. However, cash improved to $4,219,099 by March 31, 2026 after a $5,000,000 Series E preferred round and new convertible notes.

Management points to state-funded firefighter cancer screening programs, additional customer agreements, and the commercial launch of OneTest™ for Longevity as drivers for an expected revenue rebound in Q2 2026. Future filings will clarify how quickly these contracts and programs translate into higher revenue and margin performance.

Item 2.02 Results of Operations and Financial Condition Financial
Disclosure of earnings results, typically an earnings press release or preliminary financials.
Item 9.01 Financial Statements and Exhibits Exhibits
Financial statements, pro forma financial information, and exhibit attachments filed with this report.
Q1 2026 revenue $353,375 Three months ended March 31, 2026
Q1 2025 revenue $553,820 Prior-year quarter comparison
Q1 2026 net loss $2,174,836 Three months ended March 31, 2026
Cash and cash equivalents $4,219,099 As of March 31, 2026
Year-end 2025 cash $1,025,987 As of December 31, 2025
Series E private placement $5,000,000 Gross proceeds in February 2026
Total operating expenses $1,506,240 Three months ended March 31, 2026
Deferred revenue current $450,667 As of March 31, 2026
Multi-cancer early detection (MCED) medical
"OneTest™ for Cancer is a multi-cancer early detection (MCED) blood test"
A multi-cancer early detection (MCED) test is a single medical test, often a blood test, designed to screen for signs of many different cancers at once rather than targeting one type. Investors care because successful MCEDs could reshape healthcare by catching disease earlier, expanding screening markets, cutting long-term treatment costs, and creating large commercial and regulatory opportunities similar to how a single smartphone can replace many separate devices.
Series E convertible preferred stock financial
"Series E convertible preferred stock, $0.01 par value; 45,000 authorized; 5,000 and 0 shares issued"
Series E convertible preferred stock is a class of investment shares issued in a later-stage financing round that behave like a hybrid between a safety-first claim and an option to become ordinary shares. Think of it as a VIP ticket that gives owners priority on payments and protections if things go wrong, but can be swapped for regular shares later—important to investors because it affects payout priority, potential dilution of ownership, voting power, and the company’s implied valuation.
warrant liabilities financial
"a $0.1 million non-cash loss on the change in fair value of warrant liabilities"
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.
Nasdaq Capital Market market
"marked by our direct listing on the Nasdaq Capital Market"
The Nasdaq Capital Market is a platform where smaller, emerging companies can list their shares for trading by investors. It provides these companies with access to funding and visibility, helping them grow, much like a local marketplace where new vendors can introduce their products to potential customers. For investors, it offers opportunities to discover early-stage companies with growth potential.
Clinical Laboratory Improvement Amendments (CLIA) regulatory
"CAP accredited, Clinical Laboratory Improvement Amendments (CLIA) licensed laboratory in Gaithersburg, MD"
Clinical Laboratory Improvement Amendments (CLIA) are U.S. federal rules that set minimum quality and safety standards for medical laboratories that test human samples, covering test accuracy, staff qualifications, equipment, recordkeeping and routine inspections. For investors, CLIA acts like a regulatory "health inspection" for labs: certification is often required to legally run and sell clinical tests, so it directly affects a lab’s ability to generate revenue, enter markets and avoid regulatory risk.
Revenue $353,375
Gross profit $62,884
Net loss $2,174,836
Gross margin 17.8%
Cash and cash equivalents $4,219,099
Guidance

Management stated that, based on its current pipeline and expected fulfillment of state-funded firefighter screening orders, it expects revenue to rebound during the second quarter of 2026.

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UNITED STATES

SECURITIES AND EXCHANGE COMMISSION

Washington, D.C. 20549

 

FORM 8-K

CURRENT REPORT

 

Pursuant to Section 13 OR 15(d) of The Securities Exchange Act of 1934

 

Date of Report (Date of earliest event reported): May 20, 2026

 

20/20 BIOLABS, INC.
(Exact name of registrant as specified in its charter)

 

Delaware   001-43128   57-2272107
(State or other jurisdiction
of incorporation)
  (Commission File Number)   (IRS Employer
Identification No.)

 

15810 Gaither Road, Suite 235, Gaithersburg, MD   20877
(Address of principal executive offices)   (Zip Code)

 

240-453-6339
(Registrant’s telephone number, including area code)

 

 
(Former name or former address, if changed since last report)

 

Check the appropriate box below if the Form 8-K filing is intended to simultaneously satisfy the filing obligation of the registrant under any of the following provisions:

 

Written communications pursuant to Rule 425 under the Securities Act (17 CFR 230.425)

 

Soliciting material pursuant to Rule 14a-12 under the Exchange Act (17 CFR 240.14a-12)

 

Pre-commencement communications pursuant to Rule 14d-2(b) under the Exchange Act (17 CFR 240.14d-2(b))

 

Pre-commencement communications pursuant to Rule 13e-4(c) under the Exchange Act (17 CFR 240.13e-4(c))

 

Securities registered pursuant to Section 12(b) of the Act:

 

Title of each class   Trading Symbol(s)   Name of each exchange on which registered
Common Stock, par value $0.01   AIDX   The Nasdaq Stock Market LLC

 

Indicate by check mark whether the registrant is an emerging growth company as defined in Rule 405 of the Securities Act of 1933 or Rule 12b-2 of the Securities Exchange Act of 1934.

Emerging Growth Company

 

If an emerging growth company, indicate by check mark if the registrant has elected not to use the extended transition period for complying with any new or revised financial accounting standards provided pursuant to Section 13(a) of the Exchange Act.

 

 

 

 

Item 2.02 Results of Operations and Financial Condition.

 

On May 20, 2026, 20/20 Biolabs, Inc. (the “Company”) issued a press release regarding its financial results for the quarter ended March 31, 2026. A copy of the press release is furnished as Exhibit 99.1 to this report.

 

The information furnished with this Item 2.02, including Exhibit 99.1, shall not be deemed “filed” for purposes of Section 18 of the Securities Exchange Act of 1934, as amended, or otherwise subject to the liabilities of that section, nor shall it be deemed incorporated by reference into any other filing under Securities Exchange Act of 1934, as amended, or the Securities Act of 1933, as amended, except as expressly set forth by specific reference in such a filing.

 

Item 9.01 Financial Statements and Exhibits.

 

(d) Exhibits

 

Exhibit No.   Description of Exhibit
99.1   Press Release issued on May 20, 2026
104   Cover Page Interactive Data File (embedded within the Inline XBRL document)

 

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 hereunto duly authorized.

 

Date: May 20, 2026 20/20 BIOLABS, INC.  
   
  /s/ Jonathan Cohen
  Name: Jonathan Cohen
  Title: Chief Executive Officer

 

 

2 

 

Exhibit 99.1

 

 

20/20 BioLabs Reports First Quarter 2026 Financial Results and Recent Operational Progress

 

State-Funded Firefighter Cancer Screening Programs Expected to Drive Meaningful Revenue Growth Beginning in Q2 2026

 

$5.0 Million Private Placement Strengthens Cash Position to $4.2 Million as of March 31, 2026

 

Recent Strategic Wins Include Evexia Diagnostics Distribution Agreement, ROKIT Healthcare CKD License, and Commercial Launch of OneTest™ for Longevity

 

Gaithersburg, MD - May 20, 2026 - 20/20 BioLabs, Inc. (Nasdaq: AIDX) (“20/20” or the “Company”), an early market entrant in AI powered laboratory-based blood tests for the early detection and prevention of cancers and chronic diseases, reported its financial and operational results for the first quarter ended March 31, 2026.

 

First Quarter & Subsequent 2026 Operational Highlights

 

Revenue of $0.4 million for Q1 2026, as compared to $0.6 million for Q1 2025. The decline was primarily due to the timing of orders from several larger customers in Q1 2026 that have ordered, or are expected to order, in Q2 or Q3 of 2026.

 

Q2 revenue is expected to benefit from Maryland fire departments seeking the Company’s OneTest™ Multi-Cancer Early Detection (“MCED”) blood test through Maryland’s state-funded firefighter cancer screening grant program.

 

Deferred revenue increased to approximately $0.5 million as of March 31, 2026, compared to $0.4 million as of December 31, 2025, providing additional visibility into upcoming revenue recognition.

 

Cash and cash equivalents totaled $4.2 million as of March 31, 2026, compared to $1.0 million as of December 31, 2025, reflecting net proceeds from the Company’s recent capital raises.

 

Subsequent to quarter-end, the Company received notice that a second state firefighter cancer screening program comparable in size to the Maryland program intends to use the Company’s MCED test. If completed as expected, the program is anticipated to contribute meaningfully to revenue in future periods. Additional details are expected to be announced in the near term.

 

Commenced trading on the Nasdaq Capital Market under the ticker symbol “AIDX” on February 19, 2026, marking 20/20’s transition to a publicly listed company.

 

Completed a $5.0 million private placement on February 19, 2026, under a preferred purchase agreement pursuant to which up to $40.0 million in capital may be raised in multiple tranches, subject to 20/20 meeting certain conditions.

 

 

 

 

Entered into an exclusive U.S. license agreement with ROKIT Healthcare to integrate advanced chronic kidney disease (“CKD”) prediction technology into the Company’s Longevity Test Program.

 

Launched OneTest™ for Longevity, a chronic disease risk assessment and management solution built with IBM¹ watsonx.ai capabilities, expanding the Company’s product portfolio beyond multi-cancer detection.

 

Provided an update on the Company’s patented protein tumor marker based, machine learning derived MCED methodology in support of recent studies suggesting the expected value of this approach for earlier-stage detection compared to stand-alone circulating tumor DNA based MCEDs.

 

Subsequent to quarter-end, on April 7, 2026, 20/20 was selected by Evexia Diagnostics to offer OneTest™ for Cancer through Evexia’s national network of over 40,000 healthcare practitioners.

 

The Medicare Multi-Cancer Early Detection Screening Act was signed into law on February 3, 2026, creating a pathway for Medicare reimbursement for MCEDs by 2028.

 

¹IBM is acting as an information technology provider only. IBM does not purport to be engaged in the practice of medicine or any other professional clinical or licensed activity. IBM’s offerings are not designed or intended to constitute protocols for delivering medical care; a substitute for professional medical advice, diagnosis, treatment or judgment; a drug, drug-adjunct technology, or drug development tool subject to quality system requirements; or medical device as defined under the laws of any jurisdiction.

 

Management Commentary

 

Chief Executive Officer Jonathan Cohen commented, “The first quarter of 2026 was a transformational period for 20/20, marked by our direct listing on the Nasdaq Capital Market, a $5.0 million private placement under a facility that may provide up to $35 million of additional capital, and important commercial and clinical milestones across both of our OneTest™ product families.”

 

“We are also executing a clear strategy to broaden distribution and product reach. In April, we were selected by Evexia Diagnostics to offer OneTest™ for Cancer through Evexia’s national network of healthcare practitioners. In the first quarter, we launched OneTest™ for Longevity, our chronic disease risk assessment solution built with IBM¹ watsonx.ai capabilities. We are now in discussions with ROKIT Healthcare of Korea about extending the Longevity test platform across East Asia under our recently announced license agreement integrating their CKD prediction technology.”

 

“With the Medicare Multi-Cancer Early Detection Screening Act now signed into law, we believe a clear federal pathway is emerging for MCED reimbursement beginning in 2028. We plan to seek Medicare coverage for OneTest™ for Cancer, supported in part by outcome data from having screened over 25,000 firefighters to date. We believe Medicare coverage would significantly expand access to OneTest™ for Cancer and substantially increase the Company’s addressable market in the United States. Our improved capital position, expanding product portfolio, and growing list of public- and private-sector customers position 20/20 for what we expect to be a year of significant revenue growth and operational progress,” concluded Cohen.

 

Chief Financial Alan Bergman added, “While first quarter revenue of $0.4 million was down year-over-year, the decrease was driven almost entirely by the timing and seasonal ordering patterns of a number of our larger legacy customers, as well as the release of funds from the State of Maryland to its fire departments. Commercial interest in and ordering of our MCED test continues to increase, and we closed more customer agreements in Q1 2026 than in the prior-year period. Subsequent to quarter-end, we also received notice that a second state firefighter cancer screening program comparable in size to the Maryland program intends to use our MCED test, which we expect to contribute to revenue in future periods. Based on our current pipeline and expected fulfillment of state-funded firefighter screening orders, we expect revenue to rebound during the second quarter and remain encouraged by the level of demand we are seeing across our core OneTest programs.”

 

2

 

 

First Quarter 2026 Financial Results

 

Total revenue for the three months ended March 31, 2026 was $0.4 million, compared to $0.6 million in the prior year period.

 

Total cost of revenue for the three months ended March 31, 2026 was $0.3 million, compared to $0.4 million in the prior year period.

 

Gross profit for the three months ended March 31, 2026 was $0.1 million, compared to $0.2 million in the prior year period. Gross margin was 17.8% in Q1 2026, compared to 29.9% in the prior year period, reflecting a shift in product mix and lower absorption of fixed laboratory costs at the lower revenue base.

 

Total operating expenses for the three months ended March 31, 2026 were $1.5 million, compared to $0.9 million in the prior year period. The increase was primarily attributable to higher sales, and general and administrative expenses associated with the Company’s transition to a Nasdaq-listed public company. Research and development expenses were $0.2 million in Q1 2026, compared to $0.1 million in the prior year period.

 

Total other expense, net was $0.7 million for the three months ended March 31, 2026, compared to other income, net, of less than $0.1 million in the prior year period. Total other expense, net, in the current quarter principally reflected a $0.3 million non-cash loss on issuance of convertible notes, $0.3 million of interest expense, and a $0.1 million non-cash loss on the change in fair value of warrant liabilities.

 

Net loss for the three months ended March 31, 2026 was $2.2 million, compared to $0.8 million in the prior year period.

 

Cash and cash equivalents totaled $4.2 million as of March 31, 2026, compared to $1.0 million as of December 31, 2025. The increase in cash reflected $5.0 million in gross proceeds from the Company’s February 2026 private placement of Series E convertible preferred stock, along with proceeds from the issuance of convertible promissory notes, partially offset by cash used in operating activities and offering costs.

 

About 20/20 BioLabs

 

20/20 BioLabs, Inc. (Nasdaq: AIDX) develops and commercializes AI-powered, laboratory-based blood tests for the early detection and prevention of cancers and chronic diseases. The Company offers two families of lab tests under the OneTest brand. OneTest™ for Cancer is a multi-cancer early detection (MCED) blood test, and OneTest for Longevity™ measures inflammatory biomarkers and is now commercially available. OneTest’s affordable, accurate, accessible tests can be conveniently utilized at home using new, upper-arm capillary collection devices that avoid painful needles. Tests are run in the Company’s College of American Pathologists (CAP) accredited, Clinical Laboratory Improvement Amendments (CLIA) licensed laboratory in Gaithersburg, MD.

 

For more information visit https://2020biolabs.com.

 

3

 

 

Forward-Looking Statements

 

Certain statements in this release are “forward-looking statements” within the meaning of Section 27A of the Securities Act of 1933, as amended, and Section 21E of the Securities Exchange Act of 1934, as amended. These forward-looking statements involve known and unknown risks and uncertainties and are based on the Company’s current expectations and projections about future events that it believes may affect its financial condition, results of operations, business strategy, and financial needs. Forward-looking statements can be identified by words such as “may,” “could,” “will,” “should,” “would,” “expect,” “plan,” “intend,” “anticipate,” “believe,” “estimate,” “predict,” “potential,” “project,” “continue,” or the negative of these terms or other comparable expressions. Actual results may differ materially from those expressed or implied by such forward-looking statements. A number of factors could cause actual results to differ materially from those contained in these forward-looking statements, including, but not limited to, the risks described in the Company’s filings with the U.S. Securities and Exchange Commission (the “SEC”), available on the SEC’s website at www.sec.gov, including the Company’s most recent Annual Report on Form 10-K, as well as in our other reports filed or furnished from time to time with the SEC. The Company undertakes no obligation to publicly update or revise any forward-looking statements to reflect events or circumstances that occur after the date of this release or to reflect the occurrence of unanticipated events, except as required by applicable law. Although the Company believes the expectations expressed in these forward-looking statements are reasonable, it cannot guarantee future results, and investors are cautioned that actual outcomes may differ materially from those anticipated.

 

Investor Relations

 

Chris Tyson

MZ Group

Direct: 949-491-8235

AIDX@mzgroup.us

 

4

 

 

20/20 BIOLABS, INC.

CONDENSED BALANCE SHEETS

(UNAUDITED)

 

   March 31,
2026
   December 31,
2025
 
         
Assets        
Current assets:        
Cash and cash equivalents  $4,219,099   $1,025,987 
Accounts receivable, net   201,481    199,954 
Inventory   104,523    116,217 
Prepaid expenses and other current assets   175,174    128,975 
Total current assets   4,700,277    1,471,133 
License agreement, net   265,518    271,143 
Property and equipment, net   45,187    56,677 
Intangible asset, net   206,801    202,264 
Right-of-use assets, net   562,507    605,289 
Deferred financing costs   -    1,507,794 
Other assets   23,057    23,057 
Total assets  $5,803,347   $4,137,357 
           
Liabilities and Stockholders’ equity          
Current liabilities:          
Accounts payable  $980,486   $868,545 
Accrued liabilities   598,335    785,784 
Accrued dividends — Series E convertible preferred stock   54,192    - 
Deferred revenue   450,667    414,871 
Derivative liability – current   -    143,382 
Convertible note   306,716    74,611 
Operating lease liability – current   189,649    175,948 
Total current liabilities   2,580,045    2,463,141 
           
Long-term liabilities:          
Convertible notes payable, net   -    619,355 
Deferred revenue – long-term   37,055    41,816 
Derivative liabilities – long-term   -    543,545 
Operating lease liability – long term   429,122    488,725 
Total long-term liabilities   466,177    1,693,441 
           
Total liabilities   3,046,222    4,156,582 
           
Commitments and contingencies (Note 9)        - 
           
Contingently redeemable convertible preferred stock:          
Series E convertible preferred stock, $0.01 par value; 45,000 authorized; 5,000 and 0 shares issued and outstanding as of March 31, 2026 and December 31, 2025, respectively; liquidation preference of $5,494,500   204,239    - 
           
Stockholders’ equity (deficit):          
Series D preferred stock, $0.01 par value; 936,329 authorized; 0 and 101,565 shares issued and outstanding as of March 31, 2026 and December 31, 2025, respectively   -    1,016 
Series C preferred stock, $0.01 par value; 3,340,909 authorized; 0 and 1,204,040 shares issued and outstanding as of March 31, 2026 and December 31, 2025, respectively   -    12,040 
Series B preferred stock, $0.01 par value; 3,569,405 authorized; 0 and 1,471,487 shares issued and outstanding as of March 31, 2026 and December 31, 2025, respectively   -    14,715 
Series A-2 preferred stock, $0.01 par value; 800,000 authorized; 0 and 442,402 shares issued and outstanding as of March 31, 2026 and December 31, 2025, respectively   -    4,424 
Series A-1 preferred stock, $0.01 par value; 978,000 authorized; 0 and 651,465 shares issued and outstanding as of March 31, 2026 and December 31, 2025, respectively   -    6,515 
Series A preferred stock, $0.01 par value; 1,303,000 authorized; 0 and 846,368 shares issued and outstanding as of March 31, 2026 and December 31, 2025, respectively   -    8,464 
Common stock, $0.01 par value; 50,000,000 authorized; 10,442,960 and 5,442,249 shares issued and outstanding as of March 31, 2026 and December 31, 2025, respectively   104,430    54,422 
Additional paid-in capital   37,870,511    33,126,398 
Accumulated deficit   (35,422,055)   (33,247,219)
Total stockholders’ (deficit) equity   2,552,886    (19,225)
Total liabilities, contingently redeemable preferred stock and stockholders’ equity  $5,803,347   $4,137,357 

5

 

 

20/20 BIOLABS, INC.

CONDENSED STATEMENTS OF OPERATIONS

(UNAUDITED)

 

   Three Months Ended March 31, 
   2026   2025 
Revenues  $353,375   $553,820 
Cost of revenues   290,491    388,025 
Gross profit   62,884    165,795 
           
Operating expenses:          
Sales, general and administrative   1,352,758    801,144 
Research and development   153,482    136,831 
Total operating expenses   1,506,240    937,975 
           
Operating loss   (1,443,356)   (772,180)
           
Other (expense) income:          
Interest expense   (267,008)   (740)
Interest income   6,653    8,458 
Loss on change in fair value of warrant liability   (148,766)   - 
Loss on issuance of convertible note   (322,359)   - 
Other expense, net   -    (115)
Total other (expense) income   (731,480)   7,603 
           
Provision for income taxes   -    - 
           
Net loss   (2,174,836)   (764,577)
Dividend on preferred stock   54,192    - 
Net loss attributable to common stockholders  $(2,120,644)  $(764,577)
           
Basic and diluted net loss per common share  $(0.28)  $(0.16)
Weighted-average common shares outstanding, basic and diluted   7,657,229    4,823,125 

 

6

 

 

20/20 BIOLABS, INC.

CONDENSED STATEMENTS OF CASH FLOWS

(UNAUDITED)

 

   Three Months Ended March 31, 
   2026   2025 
CASH FLOWS FROM OPERATING ACTIVITIES:        
Net loss  $(2,174,836)  $(764,577)
Adjustments to reconcile net loss to net cash used in operating activities:          
Depreciation and amortization   12,306    17,825 
Stock based compensation   128,440    129,650 
Amortization of license fees   5,625    5,625 
Amortization of right-of-use assets, net of liabilities   (3,120)   (1,838)
Amortization of debt discount   240,370    - 
Issuance of shares for services   100,000    - 
Change in fair value of derivative liability   148,766    - 
Loss on issuance of convertible note   322,359    - 
Changes in operating assets and liabilities:          
Accounts receivable   (1,527)   5,610 
Inventory   11,694    (20,866)
Prepaid expenses and other assets   (46,199)   (64,259)
Accounts payable   111,941    111,092 
Accrued liabilities   (202,448)   129,413 
Interest payable   26,634    740 
Deferred revenue   31,035    (36,708)
Net cash used in operating activities   (1,288,960)   (488,293)
           
CASH FLOWS FROM INVESTING ACTIVITIES:          
Purchases of intangible assets, including patents   (5,354)   - 
Net cash used in investing activities   (5,354)   - 
           
CASH FLOWS FROM FINANCING ACTIVITIES:          
Proceeds from issuance of convertible notes payable   250,000    70,000 
Proceeds from issuance of Series D preferred stock   -    192,338 
Proceeds from issuance of Series E preferred stock   5,000,000    - 
Offering costs   (762,574)   - 
Net cash provided by financing activities   4,487,426    262,338 
           
Increase (decrease) in cash and cash equivalents   3,193,112    (225,955)
Cash and cash equivalents, beginning of year   1,025,987    1,784,009 
Cash and cash equivalents, end of year  $4,219,099   $1,558,054 
           
Supplemental disclosures of cash flow information:          
Cash paid for interest  $-   $- 
Cash paid for income taxes  $-   $- 
           
Non-cash disclosures of cash flow information:          
Conversion of preferred stock to common stock  $47,174   $- 
Deferred offering costs – issuance of common stock and warrants as offering costs  $3,654,057   $- 
Accrued dividends on Series E preferred stock  $54,192   $- 
Derivative liabilities recognized as debt discounts  $541,199   $- 
Derivative liabilities reclassified to equity  $1,361,306   $- 
Conversion of convertible notes payable and accrued interest to common stock  $834,812   $- 

 

 

7

 

FAQ

How did 20/20 BioLabs (AIDX) perform financially in Q1 2026?

20/20 BioLabs reported Q1 2026 revenue of $353,375 and a net loss of $2,174,836. Revenue declined from $553,820 a year earlier, while higher operating costs and non-cash financing-related charges widened losses as the company scaled its public-company operations.

What is 20/20 BioLabs’ cash position as of March 31, 2026?

As of March 31, 2026, 20/20 BioLabs held $4,219,099 in cash and cash equivalents. This increased from $1,025,987 at December 31, 2025, primarily due to a $5,000,000 Series E preferred stock private placement and proceeds from convertible promissory notes.

How did 20/20 BioLabs’ revenue and margins change year over year?

Q1 2026 revenue was $353,375, down from $553,820 in Q1 2025, and gross profit was $62,884. Gross margin decreased to 17.8% from 29.9%, mainly because of product mix changes and lower absorption of fixed laboratory costs at a reduced revenue base.

What financing activities did 20/20 BioLabs (AIDX) complete in early 2026?

20/20 BioLabs completed a $5,000,000 private placement of Series E convertible preferred stock and raised $250,000 from convertible notes. These activities, partially offset by $762,574 of offering costs, significantly strengthened its balance sheet and funded operations in Q1 2026.

What operational milestones did 20/20 BioLabs highlight for Q1 2026?

The company cited state-funded firefighter cancer screening programs, a new distribution agreement with Evexia Diagnostics, a CKD technology license with ROKIT Healthcare, and the commercial launch of OneTest™ for Longevity as key milestones supporting future revenue growth.

How is 20/20 BioLabs using state-funded firefighter cancer screening programs?

20/20 BioLabs has screened over 25,000 firefighters with its OneTest™ for Cancer multi-cancer early detection test. Management expects state-funded firefighter cancer screening programs, including a second state program, to contribute to revenue growth beginning in the second quarter of 2026.

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