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bioAffinity granted Hong Kong lung cancer patent

bioAffinity Technologies secures a Hong Kong patent that extends CyPath Lung’s intellectual property coverage across key Asian and global markets.

(High)
(Neutral)
Form Type
8-K

Rhea-AI Filing Summary

bioAffinity Technologies, Inc. (BIAF) reports that the Hong Kong Intellectual Property Department has granted a patent for its proprietary technology used to predict the likelihood of lung cancer by applying flow cytometry and fluorescent markers to characterize cell populations in sputum. Hong Kong Patent No. HK40048460, titled “System and Method for Determining Lung Health”, covers the use of defined antibodies and the porphyrin TCPP to label sputum cell populations and detect lung cancer cells via flow cytometry. This patent builds on a 2025 patent granted in China and contributes to a broader patent estate that includes multiple patents and pending applications in the United States, Australia, Canada, China, the European Union, Japan, Mexico and Singapore, supporting the CyPath® Lung diagnostic and other pipeline tests. The company highlights CyPath Lung’s noninvasive use in high-risk patients with small indeterminate lung nodules and cites published clinical trial results showing 92% sensitivity, 87% specificity, 88% accuracy and 99% negative predictive value in detecting lung cancer.

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Filing Explained

The filing limits the cited CyPath Lung results to the lung-cancer detection setting: it says they have not been separately validated for post-treatment surveillance, and describes the test as a Laboratory Developed Test that is not intended to be used as the sole diagnostic tool.

Item 8.01 Other Events Other
Voluntary disclosure of events the company deems important to shareholders but not covered by other items.
Item 9.01 Financial Statements and Exhibits Exhibits
Financial statements, pro forma financial information, or exhibit attachments filed with this report.
Estimated new lung cancer cases in Asia 1.6 million cases annually Company-cited estimate of annual lung cancer incidence across Asia
CyPath Lung sensitivity 92% Published clinical trial in high-risk patients with small indeterminate nodules
CyPath Lung specificity 87% Published clinical trial performance for early lung cancer detection
CyPath Lung accuracy 88% Published clinical trial in high-risk patients
CyPath Lung negative predictive value 99% Published clinical trial performance in detection setting
Hong Kong Patent Number HK40048460 Patent titled “System and Method for Determining Lung Health” granted in Hong Kong
Lung nodule size in trial Less than 20 millimeters Size of small indeterminate lung nodules in the CyPath Lung clinical trial
flow cytometry medical
"predicting the likelihood of lung cancer using flow cytometry and fluorescent markers"
A laboratory method that uses lasers and sensors to count and analyze individual cells or tiny particles as they flow past a detector, like a high‑speed supermarket scanner that reads barcodes on each item. Investors care because flow cytometry is widely used in drug development, diagnostics and manufacturing quality control; demand for the instruments, reagents and services can signal progress in clinical programs, recurring revenue streams and adoption of new therapies or tests.
negative predictive value financial
"demonstrated 92% sensitivity, 87% specificity, 88% accuracy and 99% negative predictive value"
Negative predictive value is a measure of how reliable a negative result is in confirming that a person or situation is truly free of a problem or condition. For investors, it indicates the likelihood that a negative signal or indicator truly means there is no risk or issue present, helping them assess how much trust to place in avoiding potential problems based on current information.
Laboratory Developed Test regulatory
"CyPath Lung is marketed as a Laboratory Developed Test (LDT)"
A laboratory developed test is a medical diagnostic created, validated and performed within a single clinical laboratory rather than sold as a boxed product to other labs or clinics. For investors, LDTs can offer faster product rollout and niche revenue streams like a custom service, but they also carry regulatory and reimbursement uncertainty and competitive risk—think of them as a handmade tool that can be quickly offered to customers but may face shifting rules or market limits.
Clinical Laboratory Improvement Amendments regulatory
"LDTs are overseen under the Clinical Laboratory Improvement Amendments (CLIA)"
A U.S. federal regulatory program that sets quality, certification, and inspection rules for laboratories that perform tests on human specimens to diagnose, prevent, or treat disease. It requires labs to meet standards for personnel, equipment, procedures, and result accuracy, and to obtain appropriate certificates before reporting patient results. It matters to investors because compliance affects a lab’s ability to operate, sell tests, and generate revenue, and can influence costs, inspection risk, reimbursement, and market access—similar to a licensing and safety-inspection system for labs.
porphyrin TCPP medical
"use of defined antibodies and the porphyrin TCPP to label cell populations"

FAQ

AI-generated questions and answers. How Rhea-AI works. Not financial advice.

What did bioAffinity Technologies (BIAF) announce in this 8-K filing?

bioAffinity Technologies announced that the Hong Kong Intellectual Property Department granted a patent covering its platform technology for predicting the likelihood of lung cancer using flow cytometry and fluorescent markers applied to sputum cell populations.

How does the new Hong Kong patent relate to bioAffinity Technologies’ CyPath Lung test (BIAF)?

The Hong Kong patent covers the core technology underlying CyPath Lung, including use of defined antibodies, porphyrin TCPP, and flow cytometry to analyze sputum. This technology is described as the scientific foundation of CyPath Lung, the company’s principal commercial noninvasive lung cancer diagnostic.

What clinical performance metrics for CyPath Lung does BIAF report?

In a published clinical trial of high-risk patients with small indeterminate nodules under 20 millimeters, CyPath Lung demonstrated 92% sensitivity, 87% specificity, 88% accuracy, and a 99% negative predictive value for detecting lung cancer.

How large is the potential Asian market for CyPath Lung according to BIAF?

The company cites an estimate of 1.6 million new lung cancer cases annually across Asia, describing the region as a substantial potential market for noninvasive technologies like CyPath Lung aimed at supporting earlier detection and clinical decision-making.

In which regions does bioAffinity Technologies (BIAF) report patent coverage for its lung health technology?

bioAffinity Technologies states that its global patent estate spans multiple patents and pending applications in the United States and other jurisdictions including Australia, Canada, China, the European Union, Japan, Mexico, Singapore and now Hong Kong.

What is CyPath Lung’s regulatory and commercialization status as described by BIAF?

CyPath Lung is marketed as a Laboratory Developed Test (LDT) by Precision Pathology Laboratory Services, a bioAffinity subsidiary. LDTs are overseen under the Clinical Laboratory Improvement Amendments (CLIA), and CyPath Lung is not intended for use as a sole diagnostic tool.

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false 0001712762 0001712762 2026-09-17 2026-09-17 0001712762 BIAF:CommonStockParValue0.007PerShareMember 2026-09-17 2026-09-17 0001712762 BIAF:WarrantsToPurchaseCommonStockMember 2026-09-17 2026-09-17 iso4217:USD xbrli:shares iso4217:USD xbrli:shares

 

 

 

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): September 17, 2026

 

bioAffinity Technologies, Inc.

(Exact name of registrant as specified in its charter)

 

Delaware   001-41463   46-5211056

(State or other jurisdiction

of incorporation)

 

(Commission

File Number)

 

(I.R.S. Employer

Identification Number)

 

3300 Nacogdoches Road, Suite 216

San Antonio, Texas 78217

(Address of principal executive offices, including zip code)

 

(210) 698-5334

(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 (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))

 

Title of each class   Trading Symbols   Name of each exchange on which registered

Common Stock, par value $0.007 per share

 

 

 

BIAF

 

 

The Nasdaq Stock Market LLC

(Nasdaq Capital Market)

         
Warrants to purchase Common Stock   BIAFW  

The Nasdaq Stock Market LLC

(Nasdaq Capital Market)

 

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

 

If an emerging growth company, indicate by checkmark 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 8.01. Other Events.

 

On September 17, 2026, bioAffinity Technologies, Inc., a Delaware corporation (the “Company”), issued a press release announcing that the Hong Kong Intellectual Property Department has granted a patent for the Company’s proprietary technology for predicting the likelihood of lung cancer using flow cytometry and fluorescent markers to characterize cell populations in sputum.

 

A copy of the press release is attached hereto as Exhibit 99.1 and is incorporated herein by reference.

 

Item 9.01. Financial Statements and Exhibits.

 

(d) Exhibits.

 

Exhibit
Number
  Description
99.1   Press Release issued by bioAffinity Technologies, Inc., dated September 17, 2026
104   Cover Page Interactive Data File (embedded within the 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: September 17, 2026 BIOAFFINITY TECHNOLOGIES, INC.
   
  By: /s/ Maria Zannes
  Name: Maria Zannes
  Title: President and Chief Executive Officer

 

-3-

 

 

Exhibit 99.1

 

 

bioAffinity Technologies Announces Grant of Hong Kong Patent for Company’s CyPath® Lung Noninvasive Lung Cancer Diagnostic

 

Dual patent protection in Hong Kong and China strengthens CyPath Lung’s positioning to enter Asian market

 

Asia accounts for nearly two-thirds of lung cancer cases worldwide

 

SAN ANTONIO, Texas – September 17, 2026 – bioAffinity Technologies, Inc. (Nasdaq: BIAF; BIAFW), a biotechnology company developing noninvasive healthcare solutions for the early detection and monitoring of lung disease, today announced that the Hong Kong Intellectual Property Department has granted a patent for the Company’s proprietary platform technology for predicting the likelihood of lung cancer using flow cytometry and fluorescent markers to characterize cell populations in sputum.

 

“The grant of this patent in Hong Kong and the 2025 patent we received from China strengthen the intellectual property protection for our technology in Asia, a region with a substantial burden of lung cancer,” said Maria Zannes, President and CEO of bioAffinity Technologies. “With an estimated 1.6 million new lung cancer cases diagnosed annually across Asia,1 the region represents a significant potential market for noninvasive technologies like CyPath® Lung that support earlier detection and more informed clinical decision-making that can lead to better patient outcomes.”

 

Hong Kong Patent No. HK40048460, titled “System and Method for Determining Lung Health,” covers, as described in the patent claims, 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 the sputum. The patented technology is the scientific foundation underlying CyPath Lung, which remains the centerpiece of the Company’s commercial efforts, providing physicians with a noninvasive tool to assess the likelihood of malignancy in lung nodules detected by low-dose CT scans and incidental imaging.

 

The Hong Kong patent complements bioAffinity’s expanding global patent estate, which now covers multiple patents and pending applications in the United States and other international jurisdictions, including Australia, Canada, China, the European Union, Japan, Mexico and Singapore. Together, these patents safeguard the core technology that powers the CyPath Lung test and other diagnostics in the Company’s pipeline.

 

 

1 Source: International Agency for Research on Cancer (IARC), World Health Organization, Global Cancer Observatory, GLOBOCAN 2022: Lung Cancer Fact Sheet.

 

 

 

 

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. These clinical performance data relate to CyPath Lung’s use in the detection setting and have not been separately validated for post-treatment surveillance. The high NPV may help inform physician decision-making when evaluating whether further invasive procedures are warranted. 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 or other diagnostic products in the United States or internationally; the Company’s ability to obtain and maintain patent protection and defend its intellectual property rights in the United States and foreign jurisdictions; uncertainties regarding the enforceability of patents in foreign jurisdictions, including Hong Kong and China; the Company’s ability to obtain regulatory approvals or clearances required to market its products in international markets; the accuracy of third-party estimates of market size and lung cancer incidence; the Company’s need for additional capital and its ability to obtain financing on acceptable terms; and 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

 

 

 

Filing Exhibits & Attachments

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