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bioAffinity Technologies Reports Accelerating Sales Growth of CyPath® Lung

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bioAffinity Technologies, Inc. (Nasdaq: BIAF; BIAFW) reports a 375% growth in CyPath® Lung tests ordered and processed over the past three months. The company attributes this growth to the introduction of a reimbursement code, completion of branding, and expansion of the sales force. The successful integration of the commercial laboratory has also contributed to the increasing physician interest and adoption of the noninvasive test for early-stage lung cancer.
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The reported 375% growth in CyPath® Lung tests ordered and processed by bioAffinity Technologies indicates a substantial uptick in product adoption, which could signal a positive trajectory for the company's revenue stream. The introduction of a new reimbursement code likely played a pivotal role in this growth, as it directly affects the affordability and, consequently, the accessibility of the test for patients. Furthermore, this aligns with the company's strategic steps towards refining its market positioning in Texas before scaling nationwide.

From a market perspective, the lung cancer diagnostics market is expected to reach $4.7 billion by 2030. bioAffinity's growth and alignment with market expectations may enhance investor confidence and could be reflected in the company's stock performance. However, investors should also consider the competitive landscape and the company's ability to maintain and increase market share amidst potential new entrants and existing competitors.

The emphasis on noninvasive cancer detection methods, like the CyPath® Lung test, represents a significant advancement in oncology. Noninvasive tests can lead to increased screening rates, early-stage cancer detection and improved patient outcomes. The successful integration and operation of the company's commercial laboratory, Precision Pathology Laboratory, are critical for maintaining the test's reliability and efficiency, which are key determinants of physician adoption and patient satisfaction.

bioAffinity Technologies' reported alignment with its sales growth expectations is an encouraging sign for stakeholders. However, it is essential to monitor ongoing clinical data and real-world performance to ensure that the CyPath® Lung test continues to meet medical standards and gain traction in the broader medical community.

The financial implications of bioAffinity Technologies' sales forecast meeting and the reported growth rate are of particular interest to investors. The company's ability to meet its sales forecast for the limited test market launch in Texas provides a tangible measure of its current business strategy's effectiveness. As the company prepares to release its financial results for the fourth quarter and full year, stakeholders will be looking for evidence of sustainable growth and profitability.

Investors should also consider the implications of the test's market adoption on long-term financial health, including potential impacts on operating margins and R&D expenditures as the company scales. The anticipated financial results release will offer a more comprehensive picture of the company's financial position and should be analyzed in conjunction with these growth metrics.

Increasing physician interest, newly approved reimbursement code driving growth

SAN ANTONIO--(BUSINESS WIRE)-- bioAffinity Technologies, Inc. (Nasdaq: BIAF; BIAFW), a biotechnology company focused on the need for noninvasive tests for the detection of early-stage cancer and lung disease, today reported accelerating growth of 375% in CyPath® Lung tests ordered and processed over the past three months as compared to the previous three months. CyPath® Lung is a noninvasive test to detect early-stage lung cancer.

bioAffinity Technologies is on target to meet its sales forecast for the previously announced limited test market launch in Texas designed to refine future positioning and strategic insight for CyPath® Lung in preparation for expanding to the national market.

“The introduction of our reimbursement code, completion of our branding, and expansion of our sales force have markedly contributed to the growing physician interest and adoption of our innovative, noninvasive CyPath® Lung test. Increasing physician satisfaction and adoption have also been driven by the successful integration and efficient operation of our commercial laboratory, Precision Pathology Laboratory,” bioAffinity Technologies’ President and CEO Maria Zannes said. “Importantly, our sales growth has been in line with our expectations and bolsters our confidence in our ability to capitalize on the lung cancer diagnostics market projected to reach $4.7 billion by 2030.”

Pulmonologists and other lung health specialists understand the critically important role of screening and early diagnosis in improving outcomes for those diagnosed with lung cancer and providing peace of mind for individuals at elevated risk of developing the disease. bioAffinity Technologies' commitment to noninvasive cancer detection is poised to reshape the landscape of lung health management by increasing early detection and treatment.

bioAffinity Technologies will release financial results for the fourth quarter and full year ended December 31, 2023, on April 1, 2024.

About CyPath® Lung

CyPath® Lung uses advanced flow cytometry and artificial intelligence (AI) to identify cell populations in patient sputum that indicate malignancy. Automated data analysis helps determine if cancer is present or if the patient is cancer-free. CyPath® Lung incorporates a fluorescent porphyrin, TCPP, that is preferentially taken up by cancer and cancer-related cells. Clinical study results demonstrated that CyPath® Lung had 92% sensitivity, 87% specificity and 88% accuracy in detecting lung cancer in patients at high risk for the disease who had small lung nodules less than 20 millimeters. Diagnosing and treating early-stage cancer can improve outcomes and increase patient survival.

About bioAffinity Technologies, Inc.

bioAffinity Technologies, Inc. addresses the need for noninvasive diagnosis of early-stage cancer and 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. Research and optimization of the Company’s platform technologies are conducted in its laboratories at Precision Pathology and The University of Texas at San Antonio. For more information, visit www.bioaffinitytech.com and follow us on LinkedIn, Facebook and X.

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 based upon current estimates and assumptions and include statements regarding the Company being on target to meet its sales forecast for the previously announced limited test market launch in Texas, the Company’s ability to capitalize on the lung cancer diagnostics market projected to reach $4.7 billion by 2030 and the Company’s commitment to noninvasive cancer detection being poised to reshape the landscape of lung health management by increasing early detection and treatment. 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 continue to meet its forecast and capitalize on the lung cancer diagnostics market, and the other factors discussed in the Company’s Annual Report on Form 10-K for the year ended December 31, 2022, 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.

bioAffinity Technologies

Julie Anne Overton

Director of Communications

jao@bioaffinitytech.com

Investor Relations

Dave Gentry

RedChip Companies Inc.

1-800-RED-CHIP (733-2447) or 407-491-4498

BIAF@redchip.com

Source: bioAffinity Technologies, Inc.

The ticker symbol for bioAffinity Technologies, Inc. is BIAF.

bioAffinity Technologies reported a 375% growth in CyPath® Lung tests ordered and processed over the past three months.

bioAffinity Technologies will release financial results for the fourth quarter and full year ended December 31, 2023, on April 1, 2024.

The introduction of a reimbursement code, completion of branding, expansion of the sales force, and successful integration of the commercial laboratory have contributed to the increasing physician interest and adoption of CyPath® Lung test.

The lung cancer diagnostics market is projected to reach $4.7 billion by 2030.
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About BIAFW

addressing a critical need to find cancer early and treat cancer specifically bioaffinity technologies, inc. develops tests and therapies to detect and treat cancer at the cellular level. our first product, cypath® flow cytometry for lung cancer (cypath® lung), has been licensed by precision pathology services for continued development and commercial sale as a laboratory developed test. cypath® lung has the potential to dramatically increase overall diagnostic accuracy leading to increased survival, fewer unnecessary invasive procedures and lower patient anxiety and medical costs.