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Why Is Small-Cap Cancer Focused Vincerx Pharma Stock Plummeting On Tuesday?

Why Is Small-Cap Cancer Focused Vincerx Pharma Stock Plummeting On Tuesday?

爲什麼專注於癌症的小盤股Vincerx Pharma股票在週二暴跌?
Benzinga ·  04/09 22:29

On Monday, Vincerx Pharma Inc (NASDAQ:VINC) presented preliminary Phase 1 data for VIP236 and updates on pipeline progress at the American Association for Cancer Research Annual Meeting 2024.

週一,Vincerx Pharma Inc(納斯達克股票代碼:VINC)在美國癌症研究協會2024年年會上公佈了 VIP236 的初步第一階段數據和研發進展的最新情況。

VNC-236-101 is a Phase 1 dose-escalation study with monotherapy VIP236 for metastatic tumor patients who have exhausted all standard therapy options.

VNC-236-101 是一項 1 期劑量遞增研究,採用單一療法 VIP236,適用於已用盡所有標準療法的轉移性腫瘤患者。

  • Fifteen patients have been dosed to date on the once-every-three-weeks (Q3W) schedule:
  • The Q3W schedule is well tolerated with no dose-limiting toxicity (DLT) in any patients, and no patients have discontinued VIP236 due to an adverse event.
  • No severe or life-threatening diarrhea has been observed, validating the purposeful design of VIP236's optimized camptothecin payload.
  • Seven patients have achieved objective stable disease, including tumor reduction. Four patients remain on the study, with the longest-treated patient for 168 days.
  • 迄今爲止,已按照每三週一次(Q3W)的時間表給15名患者服藥:
  • Q3W 計劃耐受性良好,對任何患者均無劑量限制毒性 (DLT),也沒有患者因不良事件停藥 VIP236。
  • 沒有觀察到嚴重或危及生命的腹瀉,這驗證了 VIP236 優化的喜樹鹼有效載荷的有針對性的設計。
  • 七名患者實現了客觀穩定的疾病,包括腫瘤減少症。四名患者仍在研究中,接受治療時間最長的患者爲168天。

VNC-943-101 is a Phase 1 dose-escalation study with monotherapy VIP943 for CD123+ acute myeloid leukemia, B-cell acute lymphocytic leukemia, or myelodysplastic syndromes.

VNC-943-101 是一項 1 期劑量遞增研究,採用單一療法 VIP943 治療 CD123+ 急性髓系白血病、B 細胞急性淋巴細胞白血病或骨髓增生異常綜合徵。

  • VIP943 is administered once per week.
  • No DLTs occurred in Cohort 1 and 2. Four patients have been enrolled in Cohort 3 (0.7 mg/kg) and are undergoing DLT assessment.
  • VIP943 PK data shows very little free payload in circulation, consistent with the favorable safety profile observed preclinically and clinically.
  • VIP943 每週給藥一次。
  • 隊列 1 和 2 中未發生 DLT。四名患者已加入隊列3(0.7 mg/kg),並正在接受DLT評估。
  • VIP943 PK數據顯示,流通中的自由有效載荷很少,這與臨床前和臨床觀察到的良好安全性相一致。

Vincerx will present additional Phase 1 data for VIP236 and VIP943 on or around the 2024 European Hematology Association Annual Meeting in June 2024.

Vincerx 將在 2024 年 6 月的 2024 年歐洲血液學協會年會上或前後公佈 VIP236 和 VIP943 的其他 1 期數據。

Vincerx also reported preclinical experiments applying the next-generation effector chemistry of its VersAptx platform to the antibodies of approved antibody-drug conjugates (ADCs), Trodelvy and Enhertu, demonstrating the potential to improve tumor toxicity of ADCs by orders of magnitude.

Vincerx還報告了將其VersaptX平台的下一代效應化學應用於已批准的抗體藥物偶聯物(ADC)Trodelvy和Enhertu的抗體的臨床前實驗,表明ADC的腫瘤毒性有可能提高几個數量級。

  • In in vitro tumor models, Vincerx's sacituzumab-legumain-KSPi ADC had a 20-fold improvement in tumor toxicity compared with Trodelvy (sacituzumab-govitecan).
  • The company's trastuzumab-legumain-KSPi ADC demonstrated an 8-fold increase in tumor toxicity compared with Enhertu (fam-trastuzumab-deruxtecan).
  • 在體外腫瘤模型中,與Trodelvy(sacituzumab-govitecan)相比,Vincerx的Sacituzumab-Legumain-KSPI ADC的腫瘤毒性提高了20倍。
  • 該公司的Trastuzumab-Legumain-KSPI ADC顯示,與Enhertu(fam-trastuzumab-deruxtecan)相比,腫瘤毒性增加了8倍。

Price Action: VINC shares are down 73.30% at $1.27 on the last check Tuesday.

價格走勢:在週二的最後一次支票中,VINC股價下跌73.30%,至1.27美元。

Photo via Shutterstock

照片來自 Shutterstock

譯文內容由第三人軟體翻譯。


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