bioAffinity Technologies (Nasdaq: BIAF) posts Q2 2026 revenue rise and 216% test surge
Rhea-AI Filing Summary
bioAffinity Technologies, Inc. reported net revenue of $1,510,579 for the quarter ended June 30, 2026, up 19% from $1,269,483 a year earlier, primarily from higher sales of its CyPath Lung diagnostic test. Net loss was $3,366,082 versus $4,060,787 in the prior-year quarter.
CyPath Lung test volume rose 216% year over year in Q2, and related testing revenue for the first six months of 2026 grew 159% to approximately $835,000, with 1,097 test reports delivered versus 390 a year earlier. Operating expenses increased to $4,845,443, reflecting higher clinical development and commercialization costs. Cash and cash equivalents were $2,429,719 as of June 30, 2026, after a June public offering that generated about $3.2 million in gross proceeds. The company advanced a longitudinal clinical trial for CyPath Lung and expanded its pipeline in asthma, COPD, and skin cancer therapeutics.
Positive
- CyPath Lung adoption accelerating: Q2 2026 test volume increased 216% year over year, with first-half CyPath Lung testing revenue up 159% to approximately $835,000, indicating rapid growth in clinical use of the company’s flagship diagnostic.
- Revenue growth and narrower loss: Q2 2026 net revenue rose 19% to $1,510,579 while net loss decreased to $3,366,082 from $4,060,787, showing improved top line and reduced quarterly losses.
Negative
- Declining cash balance and listing risk: Cash and cash equivalents fell to $2,429,719 at June 30, 2026 from $6,449,782 at December 31, 2025, and the company notes receipt of a Nasdaq delisting determination notice, which it intends to appeal.
Filing Explained
Enrollment has begun at 11 sites, while common shares outstanding rose to 6,783,061 from 4,498,675, potentially reducing unchanged holders’ ownership percentages.
This Form 8-K furnishes bioAffinity Technologies’ second-quarter 2026 results and business updates through an attached press release; the disclosed program state is that its longitudinal CyPath Lung trial has begun patient enrollment at 11 clinical sites.
Its June 30 balance sheet reports 6,783,061 common shares issued and outstanding, versus 4,498,675 on December 31, 2025; if an existing holder’s share count did not change, that larger total can reduce the holder’s percentage ownership.
The trial milestone is commencement, not completion: enrollment is reported at 11 sites, including nine VA and military medical centers, and the study is designed to evaluate clinical performance.
The filing-specific item to track is further enrollment or clinical-performance reporting for that longitudinal trial.
8-K Event Classification
Key Figures
Key Terms
longitudinal clinical trial medical
Laboratory Developed Test regulatory
negative predictive value medical
flow cytometry technical
siRNAs medical
Clinical Laboratory Improvement Amendments regulatory
Earnings Snapshot
AI-generated analysis. How Rhea-AI works. Not financial advice.
FAQ
How did bioAffinity Technologies (BIAF) perform financially in Q2 2026?
What growth did bioAffinity Technologies (BIAF) see for its CyPath Lung test?
What is bioAffinity Technologies’ (BIAF) cash position as of June 30, 2026?
How accurate is the CyPath Lung test offered by bioAffinity Technologies (BIAF)?
What pipeline developments did bioAffinity Technologies (BIAF) highlight for Q2 2026?
Is there any Nasdaq listing risk disclosed by bioAffinity Technologies (BIAF)?
UNITED STATES
SECURITIES AND EXCHANGE COMMISSION
Washington, D.C. 20549
FORM
CURRENT REPORT
Pursuant to Section 13 or 15(d) of the Securities Exchange Act of 1934
Date
of Report (Date of earliest event reported):
(Exact name of registrant as specified in its charter)
| (State
or other jurisdiction of incorporation) |
(Commission
File Number) |
(I.R.S.
Employer Identification Number) |
(Address of principal executive offices and Registrant’s telephone number, including area code)
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 (see General Instruction A.2. below):
| 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)) |
Indicate by check mark whether the registrant is an emerging growth company as defined in Rule 405 of the Securities Act of 1933 (§230.405 of this chapter) or Rule 12b-2 of the Securities Exchange Act of 1934 (§240.12b-2 of this chapter).
Emerging
growth company
| Title of each class | Trading Symbol(s) | Name of each exchange on which registered | ||
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 Operation and Financial Condition.
On August 7, 2026, bioAffinity Technologies, Inc., a Delaware corporation (the “Company”), issued a press release that included financial information for its second quarter ended June 30, 2026. A copy of the press release is attached as Exhibit 99.1 to this Current Report on Form 8-K.
The information in this Item 2.02 and in the press release attached as Exhibit 99.1 to this Current Report on Form 8-K shall not be deemed to be “filed” for purposes of Section 18 of the Securities Exchange Act of 1934, as amended, or otherwise subject to the liabilities of that section or Sections 11 and 12(a)(2) of the Securities Act of 1933, as amended. The information contained in this Item 2.02 and in the press release attached as Exhibit 99.1 to this Current Report on Form 8-K shall not be incorporated by reference into any filing with the U.S. Securities and Exchange Commission made by the Company, whether made before or after the date hereof, regardless of any general incorporation language in such filing.
Item 9.01. Financial Statements and Exhibits.
(d) Exhibits.
The following exhibit is furnished with this Current Report on Form 8-K:
| Exhibit | Description | |
| 99.1 | Press Release issued by bioAffinity Technologies, Inc. dated August 7, 2026 | |
| 104 | Cover Page Interactive Data File (embedded within the Inline XBRL document) |
| -2- |
SIGNATURES
Pursuant to the requirements of the Securities Exchange Act of 1934, as amended, the registrant has duly caused this Current Report on Form 8-K to be signed on its behalf by the undersigned hereunto duly authorized.
| Date: August 7, 2026 | BIOAFFINITY TECHNOLOGIES, INC. (Registrant) | |
| By: | /s/ Maria Zannes | |
| Name: | Maria Zannes | |
| Title: | President and Chief Executive Officer | |
| -3- |
Exhibit 99.1
 |
 |
bioAffinity Technologies Reports Second Quarter 2026 Results and Continued Strong Commercial Momentum for CyPath® Lung
CyPath Lung test volume increased 216% year over year in Q2 2026
Company drives physician adoption of CyPath Lung and advances longitudinal clinical trial
Pipeline expands to include development of precision diagnostics for asthma and COPD and dermally delivered skin cancer therapeutics
SAN ANTONIO, Texas – August 7, 2026 – bioAffinity Technologies, Inc. (Nasdaq: BIAF; BIAFW), a biotechnology company focused on the need for noninvasive, accurate tests for the detection of early-stage lung cancer and other lung diseases and topically delivered therapeutics for squamous and basal cell skin cancers, today reported financial results and business highlights for the quarter ended June 30, 2026.
Q2 2026 Highlights and Recent Events
| ● | CyPath® Lung diagnostic test volume increased 216% during the second quarter of 2026 compared to the second quarter of 2025. | |
| ● | CyPath Lung testing revenue for the first six months of 2026 increased 159% to approximately $835,000, compared with approximately $323,000 for the first six months of 2025. | |
| ● | The Company delivered 1,097 CyPath Lung test reports during the first six months of 2026, compared with 390 during the same period of 2025. | |
| ● | The number of physician offices and clinics ordering CyPath Lung for their patients increased 122% during the second quarter of 2026 compared to the same period in 2025. | |
| ● | Existing clients as of June 30, 2025, increased their CyPath Lung orders by 71% year over year during the first six months of 2026. | |
| ● | The longitudinal clinical trial designed to evaluate the clinical performance of the CyPath Lung test has begun patient enrollment at 11 clinical sites, including nine Department of Veterans Affairs (VA) and military medical centers. Financial support for the trial has been provided by the John P. Murtha Cancer Center Research Program (MCCRP), a research program within the Department of Surgery at the Uniformed Services University of the Health Sciences in Bethesda, Maryland. | |
| ● | Positive preliminary therapeutic data support the development of topical treatments for squamous and basal cell skin cancers, with self-delivering stabilized siRNAs selectively killing melanoma, squamous and basal carcinoma cells while sparing healthy cutaneous cells. |
| -1- |
| ● | bioAffinity presented positive research results advancing its diagnostic platform designed to identify antibody drug receptors in sputum to match patients with the most appropriate biologic therapies, including receptors for dupilumab, a leading therapy for asthma and chronic obstructive pulmonary disease (COPD), and benralizumab, another asthma therapy. | |
| ● | The Company published a comprehensive clinical review and white paper authored by Chief Medical Officer Gordon H. Downie, MD, PhD, that presents a practical clinical framework for incorporating CyPath Lung into pulmonary nodule evaluation and cancer surveillance. | |
| ● | The Company announced a collaboration with Pictor®, Inc., a targeted proteomic platform company, to support development and commercialization of bioAffinity Technologies’ next-generation diagnostic tests designed to provide a more complete picture of lung inflammation in patients with asthma and COPD. | |
| ● | The Society for Advanced Bronchoscopy (SAB) and National Association of Veterans Research Education Foundations (NAVREF) hosted webinars featuring multi-disciplinary panels of physicians who discussed CyPath Lung’s expanding role in the lung nodule care continuum. | |
| ● | bioAffinity received notification of allowance from the Mexican Institute of Industrial Property for a patent application protecting the use of defined antibodies and the porphyrin TCPP to label cell populations in sputum and the use of flow cytometry to determine the presence of lung cancer cells in sputum. | |
| ● | In June 2026, bioAffinity completed a public offering that generated approximately $3.2 million in gross proceeds to support commercialization activities, clinical development, and general corporate purposes. |
Management Commentary
“Our commercial strategy continues to gain significant traction as physicians increasingly recognize the clinical value of CyPath Lung for evaluating patients at high risk for lung cancer and surveilling lung cancer survivors for recurrence,” said Maria Zannes, President and Chief Executive Officer of bioAffinity Technologies. “During the second quarter, CyPath Lung test volume surged 216% year-over-year. This growth reflects accelerating physician adoption and clinical confidence in our technology. As more clinics integrate CyPath Lung into their standard of care workflows, peer-to-peer education is a powerful driving force behind building broader awareness of the test’s ability to provide objective data that complements traditional imaging and supports faster, more informed clinical decisions.”
Ms. Zannes continued, “Alongside our commercial momentum, we achieved critical milestones across our strategic roadmap. In the second quarter, we expanded physician education initiatives, including scientific presentations, webinars, podcasts and real-world clinical case studies. We continued to make progress in our large-scale longitudinal study that includes VA and military medical centers, expanding our outreach to veterans. By leveraging our expertise in flow cytometry and AI and our work with siRNAs, we are building a robust pipeline of precision diagnostics for the large asthma and COPD markets and even larger therapeutic markets for topically delivered drugs that treat squamous and basal cell skin cancers.”
| -2- |
Ms. Zannes concluded, “Looking ahead, our priorities for the second half of 2026 are expanding physician adoption, increasing utilization among existing customers, and introducing CyPath Lung to new healthcare systems and specialty practices, including oncology. The positive results we see from research and development of precision diagnostics and a therapeutic for skin cancers are exciting as we advance our pipeline. We believe this balanced approach positions bioAffinity to create lasting value for patients, healthcare providers and shareholders.”
Second Quarter 2026 Financial Results
Revenue for the quarter ended June 30, 2026, was $1.5 million, a 19% increase from the $1.3 million reported for the same period in 2025. The increase is primarily due to an increase in sales of CyPath Lung.
Operating expenses for the second quarter of 2026 were $4.8 million, compared with $3.8 million in the second quarter of 2025.
| ● | Direct costs and expenses for the second quarter of 2026 were $1.1 million, compared to $1 million in the prior-year period, primarily reflecting higher CyPath Lung test volume. | |
| ● | Research and development expenses increased 16% year-over-year to $362,000, driven by laboratory supply purchases and costs associated with relocating the research and development lab from the University of Texas at San Antonio to the Precision Pathology Laboratory services campus. | |
| ● | Clinical development expenses rose to $476,000 from $129,000 in the second quarter of 2025 due to costs associated with initiating the longitudinal clinical study. | |
| ● | Selling, general and administrative expenses were $2.9 million for the second quarter of 2026, up from $2.2 million in the same period last year. The increase was primarily driven by higher employee compensation, reflecting the addition of sales and administrative personnel to support the expanding commercialization of CyPath Lung. |
Net loss for the quarter ended June 30, 2026, was $3.4 million, compared with a net loss of $4.1 million for the second quarter of 2025.
Cash and cash equivalents as of June 30, 2026, were $2.4 million, compared with $6.4 million as of December 31, 2025.
| -3- |
About CyPath Lung
CyPath Lung by bioAffinity Technologies is a noninvasive test designed to improve the early detection of lung cancer in patients at high risk for the disease. CyPath Lung uses advanced flow cytometry and proprietary artificial intelligence (AI) to identify cell populations in patient sputum that indicate malignancy. CyPath Lung incorporates a fluorescent porphyrin that is preferentially taken up by cancer and cancer-related cells. In a published clinical trial of high-risk patients, CyPath Lung demonstrated 92% sensitivity, 87% specificity, 88% accuracy and 99% negative predictive value (NPV) in detecting lung cancer in patients at high risk for the disease who had small indeterminate lung nodules less than 20 millimeters. The high NPV gives physicians greater confidence that a negative result is truly negative, potentially sparing patients from unnecessary invasive and costly procedures. CyPath Lung is marketed as a Laboratory Developed Test (LDT) and is not intended for use as a sole diagnostic tool and should be considered alongside other clinical findings.
About bioAffinity Technologies, Inc.
bioAffinity Technologies, Inc. addresses the need for noninvasive diagnosis of early-stage cancer and other diseases of the lung and broad-spectrum cancer treatments. The Company’s first product, CyPath Lung, is a noninvasive test that has shown high sensitivity, specificity and accuracy for the detection of early-stage lung cancer. CyPath Lung is marketed as a Laboratory Developed Test (LDT) by Precision Pathology Laboratory Services, a subsidiary of bioAffinity Technologies. LDTs are overseen under the Clinical Laboratory Improvement Amendments (CLIA), which are administered by the Centers for Medicare & Medicaid Services. For more information, visit www.bioaffinitytech.com.
Forward-Looking Statements
Certain statements in this press release constitute “forward-looking statements” within the meaning of the federal securities laws. Words such as “may,” “might,” “will,” “should,” “believe,” “expect,” “anticipate,” “estimate,” “continue,” “predict,” “forecast,” “project,” “plan,” “intend” or similar expressions, or statements regarding intent, belief, or current expectations, are forward-looking statements. These forward-looking statements are subject to various risks and uncertainties, many of which are difficult to predict, that could cause actual results to differ materially from current expectations and assumptions from those set forth or implied by any forward-looking statements. Important factors that could cause actual results to differ materially from current expectations include, among others, the Company’s ability to successfully commercialize CyPath Lung and achieve broader market acceptance, the Company’s ability to obtain adequate financing to fund operations and development activities, risks related to the results of clinical trials and studies, the Company’s ability to obtain and maintain regulatory approvals or clearances, the Company’s ability to protect its intellectual property, competition from other companies developing similar products, changes in applicable laws or regulations, the Company’s limited operating history and history of operating losses, the Company’s receipt of a delisting determination notice from the Nasdaq Stock Market and the risks and uncertainties associated with the Company’s intent to appeal such determination and the outcome of any such appeal, and the other factors discussed in the Company’s Annual Report on Form 10-K for the year ended December 31, 2025, and its subsequent filings with the SEC, including subsequent periodic reports on Forms 10-Q and 8-K. Such forward-looking statements are based on facts and conditions as they exist at the time such statements are made and predictions as to future facts and conditions. While the Company believes these forward-looking statements are reasonable, readers of this press release are cautioned not to place undue reliance on any forward-looking statements. The information in this release is provided only as of the date of this release, and the Company does not undertake any obligation to update any forward-looking statement relating to matters discussed in this press release, except as may be required by applicable securities laws.
Contact
bioAffinity Technologies
Julie Anne Overton
Director of Communications
investors@bioaffinitytech.com
| -4- |
bioAffinity Technologies, Inc.
Condensed Consolidated Balance Sheets
| June 30, 2026 | December 31, 2025 | |||||||
| (unaudited) | ||||||||
| ASSETS | ||||||||
| Current assets: | ||||||||
| Cash and cash equivalents | $ | 2,429,719 | $ | 6,449,782 | ||||
| Accounts and other receivables, net | 894,823 | 541,962 | ||||||
| Inventory | 82,378 | 53,548 | ||||||
| Prepaid expenses and other current assets | 458,360 | 519,916 | ||||||
| Total current assets | 3,865,280 | 7,565,208 | ||||||
| Non-current assets: | ||||||||
| Property and equipment, net | 313,708 | 265,593 | ||||||
| Operating lease right-of-use asset, net | 769,270 | 334,289 | ||||||
| Finance lease right-of-use asset, net | 562,187 | 661,575 | ||||||
| Goodwill | 1,404,486 | 1,404,486 | ||||||
| Intangible assets, net | 687,639 | 716,806 | ||||||
| Other assets | 16,709 | 12,815 | ||||||
| Total assets | $ | 7,619,279 | $ | 10,960,772 | ||||
| LIABILITIES AND STOCKHOLDERS’ EQUITY | ||||||||
| Current liabilities: | ||||||||
| Accounts payable | $ | 969,845 | $ | 761,901 | ||||
| Accrued expenses | 1,414,492 | 1,717,989 | ||||||
| Unearned revenue | 31,140 | 42,405 | ||||||
| Operating lease liability, current portion | 163,276 | 139,220 | ||||||
| Finance lease liability, current portion | 79,592 | 139,490 | ||||||
| Notes payable, current portion | 22,561 | 105,161 | ||||||
| Total current liabilities | 2,680,906 | 2,906,166 | ||||||
| Non-current liabilities: | ||||||||
| Operating lease liability, net of current portion | 637,643 | 202,878 | ||||||
| Finance lease liability, net of current portion | 495,468 | 532,759 | ||||||
| Notes payable, net of current portion | 36,465 | 41,313 | ||||||
| Total liabilities | 3,850,482 | 3,683,116 | ||||||
| Commitments and contingencies | ||||||||
| Stockholders’ equity: | ||||||||
| Preferred Stock, par value $0.001 per share; 20,000,000 shares authorized; 450 shares and 700 shares issued and outstanding at June 30, 2026, and December 31, 2025, respectively | 1 | 1 | ||||||
| Common Stock, par value $0.007 per share; 350,000,000 shares authorized; 6,783,061 and 4,498,675 issued and outstanding at June 30, 2026, and December 31, 2025, respectively | 47,454 | 31,461 | ||||||
| Additional paid-in capital | 79,272,098 | 75,800,258 | ||||||
| Accumulated deficit | (75,550,756 | ) | (68,554,064 | ) | ||||
| Total stockholders’ equity | 3,768,797 | 7,277,656 | ||||||
| Total liabilities and stockholders’ equity | $ | 7,619,279 | $ | 10,960,772 | ||||
| -5- |
bioAffinity Technologies, Inc.
Unaudited Condensed Consolidated Statements of Operations
| Three Months Ended June 30, | Six Months Ended June 30, | |||||||||||||||
| 2026 | 2025 | 2026 | 2025 | |||||||||||||
| Net revenue | $ | 1,510,579 | $ | 1,269,483 | $ | 2,862,106 | $ | 3,123,080 | ||||||||
| Operating expenses: | ||||||||||||||||
| Direct costs and expenses | 1,087,837 | 1,016,602 | 2,016,473 | 2,384,462 | ||||||||||||
| Research and development | 361,575 | 311,372 | 711,282 | 678,758 | ||||||||||||
| Clinical development | 475,885 | 129,279 | 809,925 | 267,632 | ||||||||||||
| Selling, general and administrative | 2,858,590 | 2,214,561 | 6,100,192 | 4,667,110 | ||||||||||||
| Depreciation and amortization | 61,556 | 113,229 | 176,074 | 267,817 | ||||||||||||
| Total operating expenses | 4,845,443 | 3,785,043 | 9,813,946 | 8,265,779 | ||||||||||||
| Loss from operations | (3,334,864 | ) | (2,515,560 | ) | (6,951,840 | ) | (5,142,699 | ) | ||||||||
| Other income (expense): | ||||||||||||||||
| Interest income | 3,358 | 2,025 | 13,384 | 2,567 | ||||||||||||
| Interest expense | (11,688 | ) | (10,460 | ) | (26,410 | ) | (25,945 | ) | ||||||||
| Other income | 4,738 | 38,053 | 3,372 | 38,055 | ||||||||||||
| Other expense | (27,626 | ) | (483,043 | ) | (35,198 | ) | (492,685 | ) | ||||||||
| Change in fair value of warrants issued | — | (1,062,818 | ) | — | (1,062,818 | ) | ||||||||||
| Total other income (expense), net | (31,218 | ) | (1,516,243 | ) | (44,852 | ) | (1,540,826 | ) | ||||||||
| Net loss before provision for income tax expense | (3,366,082 | ) | (4,031,803 | ) | (6,996,692 | ) | (6,683,525 | ) | ||||||||
| Income tax expense | — | 28,984 | — | 37,679 | ||||||||||||
| Net loss | $ | (3,366,082 | ) | $ | (4,060,787 | ) | $ | (6,996,692 | ) | $ | (6,721,204 | ) | ||||
| Net loss per common share, basic and diluted | $ | (0.64 | ) | $ | (5.07 | ) | $ | (1.44 | ) | $ | (10.01 | ) | ||||
| Weighted average common shares outstanding | 5,226,753 | 800,637 | 4,860,753 | 671,529 | ||||||||||||
| -6- |