BioAffinity Technologies Set for Continued Expansion in 2025
BioAffinity Technologies Set for Continued Expansion in 2025
Noninvasive CyPath Lung test for lung cancer contributes to growing revenues
无创CyPath肺癌肺部检查有助于增加收入
SAN ANTONIO, TX (Dec. 12, 2024) – bioAffinity Technologies, Inc. (Nasdaq: BIAF; BIAFW), a biotechnology company focused on the need for noninvasive tests for the detection of early-stage cancer, today reported that the successful execution of its pilot marketing program and steady growth in sales of the CyPath Lung test for early detection of lung cancers have set the stage for expansion and record revenues in 2025.
德克萨斯州圣安东尼奥市(2024年12月12日)——专注于早期癌症检测需要无创检测的生物技术公司BioAffinity Technologies, Inc.(纳斯达克股票代码:BIAF;BIAFW)今天报告称,其试点营销计划的成功执行以及用于肺癌早期发现的Cypath肺测试销售的稳步增长为2025年的扩张和创纪录的收入奠定了基础。
The Company's wholly owned subsidiary Precision Pathology Laboratory Services (PPLS) is on track to report upwards of $9.4 million in 2024 revenues, more than 20% growth in annualized revenues over 2023 after accounting for the acquisition of PPLS in September 2023. The increase in revenues reflects a 1,750% increase in sales of CyPath Lung through Nov. 30, compared to the same period last year.
该公司的全资子公司精密病理学实验室服务(PPLS)有望在2024年公布超过940万美元的收入,在考虑2023年9月收购PPLS后,年化收入将比2023年增长20%以上。收入的增长反映了截至11月30日的CyPath Lung的销售额与去年同期相比增长了1750%。
"The seamless integration of Precision Pathology into bioAffinity Technologies since the acquisition is going to result in a record revenue year for the laboratory, due in part to the broader market adoption of CyPath Lung," bioAffinity President and CEO Maria Zannes said. "We count many successes in 2024, including obtaining reimbursement for CyPath Lung, expanding our sales team, obtaining access to the federal healthcare system, and streamlining operations. We have the capability and the experience to expand operations exponentially to meet the growing demand for CyPath Lung as we move to the national stage in 2025."
BioAffinity总裁兼首席执行官玛丽亚·赞内斯表示:“自收购以来,精准病理学与BioAffinity Technologies的无缝整合将使该实验室的收入创历史新高,部分原因是CyPath Lung在更广泛的市场上采用了CyPath Lung。”“我们在2024年取得了许多成功,包括获得CyPath Lung的报销、扩大我们的销售团队、获得联邦医疗系统的准入以及精简运营。随着我们在2025年进入全国舞台,我们有能力和经验成倍地扩大业务,以满足对Cypath Lung不断增长的需求。”
CyPath Lung revenues are expected to continue growing in 2025 with expanded sales into strategic national markets and inclusion in the U.S. Federal Supply Schedule. This key procurement system provides streamlined access to state-of-the-art healthcare solutions for the Veterans Health Administration (VHA) and the Military Health System. CyPath Lung fills an important need for a noninvasive test to improve the early detection of lung cancer in patients at high risk. CyPath Lung can be used alone or in combination with other diagnostic tools, positioning it as a cornerstone of next-generation lung cancer care.
预计CyPath Lung的收入将在2025年继续增长,销售将扩大到战略性全国市场,并纳入美国联邦供应计划。这一关键采购系统为退伍军人健康管理局(VHA)和军人卫生系统提供了获得最先进医疗解决方案的简便途径。CyPath Lung满足了对无创检测的重要需求,以改善高危患者对肺癌的早期发现。CyPath Lung可以单独使用,也可以与其他诊断工具结合使用,将其定位为下一代肺癌治疗的基石。
About CyPath Lung
关于 CyPath Lung
CyPath Lung uses proprietary 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, meso-tetra (4-carboxyphenyl) 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 lung cancer can improve outcomes and increase patient survival. For more information, visit .
CyPath Lung 使用专有的先进流式细胞仪和人工智能 (AI) 来识别患者痰液中表明恶性肿瘤的细胞群。自动数据分析有助于确定是否存在癌症或患者是否没有癌症。Cypath Lung 含有一种荧光卟啉即中四氯联苯 (TCPP),它优先被癌症和癌症相关细胞吸收。临床研究结果表明,对于肺结节小于20毫米的高风险患者,Cypath Lung检测肺癌的灵敏度为92%,特异性为87%,准确率为88%。诊断和治疗早期肺癌可以改善预后并提高患者的存活率。欲了解更多信息,请访问。
About bioAffinity Technologies, Inc.
关于生物亲和科技公司
bioAffinity Technologies, Inc. (Nasdaq: BIAF) 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. For more information, visit and follow us on LinkedIn, Facebook and X.
BioAffinity Technologies, Inc.(纳斯达克股票代码:BIAF)满足了对早期癌症和肺部疾病的无创诊断以及广谱癌症治疗的需求。该公司的第一款产品CyPath Lung是一种非侵入性测试,在检测早期肺癌方面显示出很高的灵敏度、特异性和准确性。CyPath Lung由BioAffinity Technologies的子公司精密病理学实验室服务作为实验室开发测试(LDT)销售。欲了解更多信息,请在 LinkedIn、Facebook 和 X 上访问并关注我们。
Forward-Looking Statements
前瞻性陈述
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 expansion and record revenues in 2025, the expected 2024 revenues from PPLS, growing demand for CyPath Lung as the Company moves to the national stage in 2025, and CyPath Lung revenues being expected to continue growing in 2025 with expanded sales into strategic national markets and inclusion in the U.S. Federal Supply Schedule. 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 ability of the Company to increase sales through the U.S. Federal Supply Schedule and the other factors discussed in the Company's Annual Report on Form 10-K for the year ended December 31, 2023, 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.
本新闻稿中的某些陈述构成联邦证券法所指的 “前瞻性陈述”。诸如 “可能”、“可能”、“将”、“应该”、“相信”、“预期”、“估计”、“继续”、“预测”、“预测”、“项目”、“计划”、“打算” 或类似表述,或有关意图、信念或当前预期的陈述,均为前瞻性陈述。这些前瞻性陈述基于当前的估计和假设,包括有关2025年扩张和创纪录收入的陈述,2024年PPLS的预期收入,随着公司进入全国舞台而对Cypath Lung的需求不断增长,以及Cypath Lung收入预计将在2025年继续增长,将销售扩大到战略性国家市场并纳入美国联邦供应计划。这些前瞻性陈述受到各种风险和不确定性的影响,其中许多风险和不确定性难以预测,这可能导致实际结果与当前的预期和假设与任何前瞻性陈述中提出或暗示的预期和假设存在重大差异。可能导致实际业绩与当前预期存在重大差异的重要因素包括公司通过美国联邦供应计划增加销售额的能力以及公司截至2023年12月31日止年度的10-k表年度报告中讨论的其他因素,以及随后向美国证券交易委员会提交的文件,包括随后的10-Q和8-k表定期报告。此类前瞻性陈述基于发表此类陈述时存在的事实和条件以及对未来事实和状况的预测。尽管公司认为这些前瞻性陈述是合理的,但提醒本新闻稿的读者不要过分依赖任何前瞻性陈述。本新闻稿中的信息仅在本新闻稿发布之日提供,除非适用的证券法有要求,否则公司没有义务更新与本新闻稿中讨论的事项有关的任何前瞻性陈述。
Contacts
联系人
bioAffinity Technologies
Julie Anne Overton
Director of Communications
jao@bioaffinitytech.com
生物亲和力技术
朱莉安妮奥弗顿
传播总监
jao@bioaffinitytech.com
Investor Relations
Dave Gentry
RedChip Companies Inc.
1-800-RED-CHIP (733-2447) Or 407-491-4498
BIAF@redchip.com
投资者关系
戴夫·金特里
RedChip 公司公司
1-800-RED-CHIP (733-2447) 或 407-491-4498
BIAF@redchip.com