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Small-Cap Cancer-Focused Nuvation Bio Pulls Plug On Early-Stage Program After Considering Phase 1 Solid Tumor Data

Small-Cap Cancer-Focused Nuvation Bio Pulls Plug On Early-Stage Program After Considering Phase 1 Solid Tumor Data

以癌症爲重點的小市值藥企Nuvation Bio在考慮了一期實體瘤數據後,中止了早期項目。
Benzinga ·  14:27

In its second-quarter earnings release, Nuvation Bio Inc. (NYSE:NUVB) announced that it has decided to halt work on NUV-868, its BD2-selective BET inhibitor, while considering the program's future.

紐交所股票代碼爲NUVB的Nuvation Bio Inc.在其第二季度業績中宣佈,已決定停止研發BD2選擇性BEt抑制劑NUV-868,同時考慮該項目的未來。

The company said it concluded the Phase 1b dose escalation study of NUV-868 in combination with AstraZeneca Plc (NASDAQ:AZN)-Merck & Co Inc's (NYSE:MRK) Lynparza (olaparib) for ovarian, pancreatic, metastatic castration-resistant prostate (mCRPC), triple-negative breast cancer, and other solid tumors, and with Pfizer Inc (NYSE:PFE)-Astellas Pharma Inc's (OTC:ALPMF) (OTC:ALPMY) Xtandi (enzalutamide) for mCRPC.

該公司表示,已完成與阿斯利康股份有限公司(納斯達克:AZN)- 默克愛文思控股公司(紐交所:MRK)Lynparza(奧拉帕尼)及輝瑞公司(紐交所:PFE)- 安斯泰萊製藥(市場外交易:ALPMF)(市場外交易:ALPMY)的Xtandi(恩扎魯胺)聯合用於卵巢、胰腺、轉移性去勢抵抗性前列腺癌(mCRPC)、三陰性乳腺癌和其他實體腫瘤的NUV-868劑量遞增研究階段。

The company completed an internal analysis of efficacy and safety data from Phase 1 monotherapy and Phase 1b combination studies of NUV-868.

該公司完成了NUV-868單藥和與其他治療方案聯合應用的Phase 1研究和劑量遞增研究的療效和安全數據的內部分析。

Following this analysis, Nuvation Bio decided not to initiate a Phase 2 study of NUV-868 as a monotherapy or combined with olaparib or enzalutamide in the advanced solid tumor indications that were part of the Phase 1 and Phase 1b study designs.

在完成這項分析後,Nuvation Bio 決定不啓動一項關於NUV-868單藥治療或與奧拉帕尼或恩扎魯胺聯合治療作爲Phase 1和劑量遞增設計的高級實體瘤適應症的Phase 2研究。

The company is evaluating the next steps for the NUV-868 program, including further development in combination with approved products for indications in which BD2-selective BET inhibitors may improve patient outcomes.

該公司正在評估NUV-868計劃的下一步工作,包括與獲批產品聯合開發,以改善BD2選擇性BEt抑制劑可能提高患者預後的適應症。

"As we focus on our late-stage pipeline and prepare to potentially bring taletrectinib to patients in the U.S. in 2025, we have decided not to initiate a Phase 2 study of NUV-868 in the solid tumor indications studied to date. This decision comes after a careful review of the data generated in the Phase 1 monotherapy study and Phase 1b study of NUV-868 in combination with olaparib or enzalutamide. We are exploring next steps for NUV-868 in new indications and will share updates as available," said David Hung, Founder, President, and CEO of Nuvation Bio.

“我們專注於晚期開發管線,並準備於2025年將泰來替尼帶給美國患者時,我們決定不在迄今研究的實體瘤適應症中啓動NUV-868的Phase 2研究。這一決定是在仔細評估NUV-868單藥研究和與奧拉帕尼或恩扎魯胺聯合應用的Phase 1研究和劑量遞增研究所生成的數據後做出的。我們正在探索NUV-868在新適應症中的下一步工作,並將根據可用情況進行更新,” Nuvation Bio的創始人、總裁和首席執行官David Hung表示。

Two years back, Nuvation Bio discontinued the clinical development of NUV-422 after an internal risk-benefit analysis factoring in feedback from the FDA in a partial clinical hold letter for monotherapy Phase 1/2 study and clinical hold letters for its combination Phase 1b/2 studies.

兩年前,Nuvation Bio在內部風險收益分析中將FDA的部分臨床暫停信和多種藥物聯合應用的臨床暫停信等反饋納入考慮,決定終止NUV-422的臨床開發。

As of June 30, 2024, Nuvation Bio had cash, cash equivalents, and marketable securities of $577.2 million.

截至2024年6月30日,Nuvation Bio的現金、現金等價物和市場證券總額爲5,772萬美元。

Price Action: NUVB stock is down 7.41% at $3.11 at last check Monday.

NUVb股票上週一最後檢查下跌7.41%,報3.11美元。

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