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NAYA Biosciences Announces Development of NY-500, a Novel AI-Optimized PD-1 x VEGF Bifunctional Antibody - NAYA Biosciences (NASDAQ:NAYA)
* PD-1 x VEGF antibodies show potential to surpass checkpoint inhibitors as standard-of-care in multiple oncology indications * NAYA aiming to initiate clinical trials in early 2026 SARASOTA, Fla. and MIAMI, Jan. 06, 2025 (GLOBE NEWSWIRE) -- NAYA Biosciences ("NAYA") NAYA, a life science portfolio company dedicated to bringing breakthrough treatments to patients in oncology, autoimmune diseases, and women's health, today announced that it is expanding its bifunctional antibody pipeline to include a novel PD-1 x VEGF tetravalent bifunctional antibody for the treatment of hepatocellular carcinoma (HCC) and other solid tumors. NAYA is leveraging its proprietary FLEX antibody platform and further optimizing its design through a partnership with MabSilico, an artificial intelligence & deep technology-focused company, to accelerate the development of new best-in-class candidates for validated therapeutic targets. "We are excited to add a novel, AI-optimized PD-1 x VEGF therapeutic candidate to our pipeline of best-in-class bifunctional antibodies," commented NAYA Biosciences President Dr. Daniel Teper. "NAYA's bifunctional format has demonstrated the ability for synergistic dual-targeting activity, resulting in the potential to unlock clinical response in solid tumors. NY-500, our PD-1 x VEGF antibody, will target hepatocellular carcinoma (HCC) and other solid tumors with high unmet medical needs. Recent clinical data with ivonescimab, the most advanced PD-1 x VEGF antibody, has shown superiority in non-small-cell lung cancer (NSCLC) compared to Keytruda®, the leading first-line immunotherapy standard-of-care in multiple solid tumors, paving the way for a new generation of PD-(L)1 therapeutic candidates." NAYA is also developing a GPC3-targeting bifunctional antibody (NY-303) in a phase 1/2 clinical trial for HCC patients not responding to PD-1 +/- VEGF therapy. NAYA has recently presented data for NY-303 at the Society for Immunotherapy of Cancer (SITC) demonstrating the ability to reverse resistance to PD-1 checkpoint blockage and turn tumors from a "cold" into a "hot" status, making the tumors susceptible to immunotherapy again. Initiation of monotherapy Phase 1/2a clinical trials has been cleared by regulatory authorities and leading academic centers and is expected to start in 2025. About NY-500 (PD-1 x VEGF Bifunctional Antibody) NY-500 is a tetravalent bifunctional antibody targeting PD-1, a key immune checkpoint targeted by pembrolizumab (Keytruda®, Merck & Co), and VEGF, a vascular endothelial growth factor targeted by bevacizumab (Avastin®, Genentech Roche) which regulates the production of new blood vessels (angiogenesis). Synergistic effects of simultaneously targeting PD-1 & VEGF have been shown to improve T-cell infiltration into tumors and enhance immune response while disrupting tumor vasculature. Ivonescimab, a PD-1 x VEGF antibody from Summit Therapeutics, recently outperformed pembrolizumab in a head-to-head lung cancer clinical trials. NY-500 has a differentiated molecular design, leveraging both NAYA's proprietary FLEX format and AI-optimization, and is expected to enter monotherapy phase 1/2a clinical trials in early 2026 for the treatment of hepatocellular carcinoma (HCC) & other solid tumors. According to IQVIA, the PD(L)1 market is expected to exceed $50 billion in 2025. About NAYA Biosciences NAYA Biosciences NAYA is a life science portfolio company dedicated to bringing breakthrough treatments to patients in oncology, autoimmune diseases, and women's health. Our proven hub & spoke model harnesses the shared resources of a parent company and agility of lean strategic franchises, enabling efficient acquisition, development, and partnering of assets and allowing for optimized return on investment by combining scalable, profitable commercial revenues with the upside of innovative clinical-stage therapeutics. NAYA's expanding portfolio of assets currently includes NY-303, a GPC3 x NKp46 bifunctional antibody for the treatment of hepatocellular carcinoma (HCC) with a unique mode of action targeting non-responders to the current immunotherapy standard of care (approximately 70% of the current treatable market) cleared to enroll patients in a Phase 1/2a monotherapy trial in 2025, NY-338, a CD38 x NKp46 bifunctional antibody for the treatment of multiple myeloma and autoimmune diseases with a differentiated safety and efficacy profile, NY-500, a PD-1 x VEGF bifunctional antibody for the treatment of HCC and other solid tumors, and NY-600 a PSMA x NKp46 bifunctional antibody for the treatment of metastatic Castration Resistant Prostate Cancer (mCRPC). This release includes 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. The Company invokes the protections of the Private Securities Litigation Reform Act of 1995. All statements regarding our expected future financial position, results of operations, cash flows, financing plans, business strategies, products and services, competitive positions, growth opportunities, plans and objectives of management for future operations, as well as statements that include words such as "anticipate," "if," "believe," "plan," "estimate," "expect," "intend," "may," "could," "should," "will," and other similar expressions are forward-looking statements. All forward-looking statements involve risks, uncertainties, and contingencies, many of which are beyond our control, which may cause actual results, performance, or achievements to differ materially from anticipated results, performance, or achievements. Factors that may cause actual results to differ materially from those in the forward-looking statements include those set forth in our filings at www.sec.gov. We are under no obligation to (and expressly disclaim any such obligation to) update or alter our forward-looking statements, whether as a result of new information, future events or otherwise. NAYA Investor & Media Contact Anna Baran-Djokovic SVP, Investor Relations +1-305-615-9162 [email protected] NAYANAYA Biosciences$1.1532.1%WatchlistOverviewMarket News and Data brought to you by Benzinga APIs
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NAYA Biosciences expands oncology pipeline with new antibody By Investing.com
SARASOTA, Fla. and MIAMI - NAYA Biosciences (NASDAQ: NAYA), a $3.9 million market cap portfolio company specializing in oncology, autoimmune diseases, and women's health, announced today its plan to introduce a novel PD-1 x VEGF bifunctional antibody into its pipeline. The company's stock has shown strong momentum with a 10.85% gain over the past week, according to InvestingPro data. This new therapeutic candidate is designed to target hepatocellular carcinoma (HCC) and other solid tumors. The company is utilizing its proprietary FLEX antibody platform and collaborating with MabSilico, a firm specializing in artificial intelligence and deep technology, to enhance the development of this antibody. With an impressive InvestingPro Financial Health Score of 3.24 (rated as GREAT), NAYA appears well-positioned to execute its development strategy. Dr. Daniel Teper, President of NAYA Biosciences, expressed enthusiasm about the potential of this AI-optimized candidate to exhibit synergistic dual-targeting activity, which could lead to improved clinical responses in solid tumors. The new antibody, named NY-500, is expected to enter monotherapy phase 1/2a clinical trials in early 2026. It targets PD-1, an immune checkpoint, and VEGF, a factor in blood vessel formation, aiming to improve T-cell infiltration and immune response while disrupting tumor vasculature. This approach follows recent clinical data indicating the effectiveness of ivonescimab, another PD-1 x VEGF antibody, in outperforming pembrolizumab in lung cancer trials. In addition to NY-500, NAYA is advancing NY-303, a GPC3-targeting bifunctional antibody, currently in phase 1/2 clinical trials for HCC patients who have not responded to existing PD-1 +/- VEGF therapies. NY-303 has shown promise in converting tumors to a status more receptive to immunotherapy. NAYA Biosciences is a NASDAQ-listed company with a hub & spoke model that facilitates the acquisition, development, and partnering of assets. Its portfolio also includes NY-338, targeting multiple myeloma and autoimmune diseases, and NY-600, for metastatic castration-resistant prostate cancer treatment. This expansion of NAYA's oncology pipeline comes as the PD(L)1 market is expected to surpass $50 billion in 2025, according to IQVIA. Trading at $0.87 per share, investors can access detailed financial analysis and additional insights through InvestingPro, which offers exclusive metrics and investment tips for NAYA Biosciences. The information disclosed is based on a press release statement from NAYA Biosciences. In other recent news, INVO Bioscience has completed its merger with NAYA Biosciences, an oncology and autoimmune disease specialist. This strategic move unites INVO's fertility business with NAYA's clinical-stage assets, aiming to leverage combined resources for enhanced growth and innovation. The newly formed entity, which will operate under the name NAYA Biosciences, will include a leadership team comprising of INVO's CEO Steve Shum and CFO Andrea Goren, and NAYA's founder Dr. Daniel Teper as President and CEO of the new NAYA Therapeutics subsidiary. The merger has also resulted in a combined company portfolio which includes a bispecific antibody targeting GPC3 for hepatocellular carcinoma patients, and a CD38-targeting bispecific antibody with potential applications in multiple myeloma and autoimmune diseases. The transaction did not require the approval of INVO's stockholders and post-merger, INVO's equity holders will own approximately 17.75% of the combined company. In addition to the merger, INVO Bioscience has secured a Merchant Cash Advance of $265,000 to support its working capital and general corporate functions. The company has also extended its merger agreement with NAYA Biosciences to October 14, 2024, with NAYA set to purchase 27,500 shares of Series A Preferred Stock for $137,500 upon completion of the merger. These are among the recent developments in INVO Bioscience's business operations.
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NAYA Biosciences announces the development of NY-500, a novel AI-optimized PD-1 x VEGF bifunctional antibody for treating hepatocellular carcinoma and other solid tumors, leveraging artificial intelligence to potentially surpass current immunotherapy standards.
NAYA Biosciences (NASDAQ: NAYA), a life science portfolio company, has announced the development of NY-500, a novel AI-optimized PD-1 x VEGF bifunctional antibody designed to treat hepatocellular carcinoma (HCC) and other solid tumors 1. This innovative approach combines the company's proprietary FLEX antibody platform with artificial intelligence optimization through a partnership with MabSilico, an AI and deep technology-focused company 1.
The use of AI in optimizing NY-500's design represents a significant step forward in drug development. By partnering with MabSilico, NAYA Biosciences aims to accelerate the creation of best-in-class candidates for validated therapeutic targets 1. This collaboration highlights the growing trend of integrating AI technologies into pharmaceutical research and development processes.
Recent clinical data with ivonescimab, another PD-1 x VEGF antibody, has shown superiority in non-small-cell lung cancer (NSCLC) compared to Keytruda®, the leading first-line immunotherapy standard-of-care in multiple solid tumors 1. This breakthrough paves the way for a new generation of PD-(L)1 therapeutic candidates, with NY-500 positioned to potentially offer improved outcomes for cancer patients.
NY-500 targets both PD-1, a key immune checkpoint, and VEGF, a vascular endothelial growth factor 1. This dual-targeting approach aims to improve T-cell infiltration into tumors and enhance immune response while disrupting tumor vasculature 1. The PD(L)1 market is expected to exceed $50 billion in 2025, according to IQVIA, highlighting the significant commercial potential for successful therapies in this space 12.
NAYA Biosciences plans to initiate monotherapy phase 1/2a clinical trials for NY-500 in early 2026 1. The company is also developing other promising candidates, including NY-303, a GPC3-targeting bifunctional antibody currently in phase 1/2 clinical trials for HCC patients not responding to existing PD-1 +/- VEGF therapies 12.
NAYA Biosciences, with a market cap of $3.9 million, employs a hub & spoke model to efficiently acquire, develop, and partner assets 2. The company recently completed a merger with INVO Bioscience, combining INVO's fertility business with NAYA's clinical-stage assets 2. This strategic move aims to leverage combined resources for enhanced growth and innovation in oncology, autoimmune diseases, and women's health 2.
Despite its relatively small market cap, NAYA Biosciences has shown strong recent performance, with a 10.85% gain in stock price over the past week 2. The company boasts an impressive InvestingPro Financial Health Score of 3.24, rated as GREAT, suggesting a solid foundation for executing its development strategy 2.
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