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NAYA Biosciences Announces Development of NY-500, a Novel AI-Optimized PD-1 X VEGF Bifunctional Antibody

NAYA Biosciences Announces Development of NY-500, a Novel AI-Optimized PD-1 X VEGF Bifunctional Antibody

NAYA生物科學公司宣佈開發NY-500,這是一種新型人工智能優化的PD-1與VEGF雙功能抗體
GlobeNewswire ·  01/06 08:30

• PD-1 x VEGF antibodies show potential to surpass checkpoint inhibitors as standard-of-care in multiple oncology indications

• PD-1 x VEGF抗體在多種腫瘤指徵中有潛力超越檢查點抑制劑,成爲標準治療方案

• NAYA aiming to initiate clinical trials in early 2026

• NAYA計劃於2026年初啓動臨牀試驗

SARASOTA, Fla. and MIAMI, Jan. 06, 2025 (GLOBE NEWSWIRE) -- NAYA Biosciences ("NAYA") (NASDAQ: 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.

佛羅里達州薩拉索塔和邁阿密,2025年1月6日(環球新聞通訊社)——NAYA生物科學(「NAYA」)(納斯達克:NAYA),一家致力於爲腫瘤學、自身免疫疾病和女性健康患者提供突破性治療的生命科學投資公司,今天宣佈其雙功能抗體管線正在擴大,新增一種用於治療肝細胞癌(HCC)和其他實體瘤的新型PD-1 x VEGF四價雙功能抗體。

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.

NAYA正在利用其專有的FLEX抗體平台,並通過與專注於人工智能與深度技術的公司MabSilico的合作進一步優化其設計,以加速驗證的治療靶點的新一流候選藥物的發展。

"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."

"我們很高興能將一個新穎的人工智能優化的PD-1 x VEGF治療候選者加入我們的一流雙功能抗體管線中," NAYA生物科學公司總裁Daniel Teper博士評論道。"NAYA的雙功能格式已證明具備協同雙靶向作用的能力,有可能在固體腫瘤中解鎖臨牀響應。NY-500,我們的PD-1 x VEGF抗體,將針對肝細胞癌(HCC)和其他具有高度未滿足醫療需求的固體腫瘤。近期關於ivonescimab的臨牀數據,作爲最先進的PD-1 x VEGF抗體,在非小細胞肺癌(NSCLC)中表現出優越性,相較於Keytruda,這是多個固體腫瘤中的主流一線免疫治療標準,鋪平了一代新的PD-(L)1治療候選者的道路。"

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.

NAYA還在進行鍼對肝細胞癌患者的GPC3靶向雙功能抗體(NY-303)1/2期臨牀試驗,針對那些對PD-1 +/- VEGF治療無反應的患者。NAYA最近在癌症免疫治療學會(海豐國際)上展示了NY-303的數據,顯示其能夠逆轉對PD-1檢查點阻斷的抵抗力,並將腫瘤從「冷」狀態轉變爲「熱」狀態,使腫瘤再次易於免疫治療。單藥治療的1/2a期臨牀試驗的啓動已獲得監管機構和領先學術中心的批准,預計將在2025年開始。

About NY-500 (PD-1 x VEGF Bifunctional Antibody)

關於NY-500(PD-1 x VEGF雙功能抗體)

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.

NY-500是一種四價雙功能抗體,靶向PD-1,這是一個關鍵免疫檢查點,默沙東的pembrolizumab(Keytruda)靶向此點,以及VEGF,這是一個血管內皮生長因數,bevacizumab(Avastin,基因科技Roche)靶向此點,這一因數調節新血管的生成(血管生成)。同時靶向PD-1和VEGF的協同效應已被證明能夠提高T細胞對腫瘤的浸潤並增強免疫反應,同時破壞腫瘤血管。來自Summit Therapeutics的ivonescimab在肺癌臨牀試驗中,最近表現優於pembrolizumab。NY-500擁有差異化的分子設計,利用NAYA專有的FLEX格式和人工智能優化,預計將在2026年初進入肝細胞癌(HCC)和其他固體腫瘤的單藥治療1/2a期臨牀試驗。根據IQVIA的數據,PD(L)1市場預計將在2025年超過500億。

About NAYA Biosciences

關於NAYA生物科學

NAYA Biosciences (NASDAQ: 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 Biosciences(納斯達克:NAYA)是一家生命科學投資組合公司,致力於爲腫瘤學、自身免疫疾病和女性健康的患者帶來突破性治療。我們經過驗證的中心和分散模式利用了母公司的共享資源和精益戰略業務的靈活性,使得資產的高效收購、開發和合作成爲可能,通過將可擴展的、盈利的商業收入與創新臨牀階段治療的潛在收益相結合,實現投資回報的優化。

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).

NAYA不斷擴展的資產組合目前包括NY-303,這是一種GPC3 x NKp46雙功能抗體,用於治療肝細胞癌(HCC),具有獨特的作用機制,針對當前免疫治療標準治療(約70%的可治療市場)的非應答者,已獲准於2025年招募患者進行1/2a期單藥臨牀試驗;NY-338,這是一種CD38 x NKp46雙功能抗體,用於治療多發性骨髓瘤和自身免疫性疾病,具有獨特的安全性和有效性;NY-500,這是一種PD-1 x VEGF雙功能抗體,用於治療HCC和其他實體瘤;以及NY-600,這是一種PSMA x NKp46雙功能抗體,用於治療轉移性去勢抵抗性前列腺癌(mCRPC)。

Safe Harbor Statement
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.

安全港聲明
本發佈包含根據1933年證券法第27A節及1934年證券交易法第21E節的定義所作的前瞻性聲明。公司尋求1995年私營證券訴訟改革法案的保護。所有關於我們預期未來財務狀況、運營結果、現金流、融資計劃、業務戰略、產品和服務、競爭地位、增長機會、管理層未來運營的計劃和目標,以及包含"預計"、"如果"、"相信"、"計劃"、"估計"、"期待"、"打算"、"可能"、"可以"、"應該"、"將"及其他類似表達的聲明都是前瞻性聲明。所有前瞻性聲明都涉及風險、不確定性和偶然性,其中許多超出我們的控制,這可能導致實際結果、表現或成就與預期結果、表現或成就有重大差異。可能導致實際結果與前瞻性聲明中的結果有重大差異的因素包括我們在www.sec.gov上的提交文件中列出的因素。我們沒有義務(並明確聲明不承擔任何此類義務)更新或更改我們的前瞻性聲明,無論是由於新信息、未來事件或其他原因。

NAYA Investor & Media Contact
Anna Baran-Djokovic
SVP, Investor Relations
+1-305-615-9162
anna@nayabiosciences.com

NAYA投資者及媒體聯繫
安娜·巴蘭-德約科維奇
高級副總裁,投資者關係
+1-305-615-9162
anna@nayabiosciences.com


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