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Why Is Repare Therapeutics Stock Trading Lower On Friday?

Why Is Repare Therapeutics Stock Trading Lower On Friday?

爲什麼Repare Therapeutics的股票在週五交易下跌?
Benzinga ·  01:09

On Thursday, Repare Therapeutics Inc (NASDAQ:RPTX) revealed data from its MYTHIC Phase 1 gynecologic expansion trial evaluating the combination of lunresertib and camonsertib (Lunre+Camo) for endometrial cancer and platinum-resistant ovarian cancer (PROC) harboring lunre-sensitizing biomarkers.

週四,Repare Therapeutics Inc(納斯達克:RPTX)公佈了其MYTHIC 1期婦科擴展試驗的數據,評估了lunresertib和camonsertib(Lunre+Camo)聯合治療有lunre敏感性生物標誌物的子宮內膜癌和鉑金抗藥性卵巢癌(PROC)。

As of the data cut-off date of November 14, 51 evaluable patients were enrolled in the gynecologic cancer expansion cohort of the MYTHIC trial.

截至2023年11月14日的數據截止日期,共有51名可評估患者被納入MYTHIC試驗的婦科癌症擴展隊列。

Across all tumor types treated at the optimized RP2D (n=67), Lunre+Camo therapy showed a favorable and differentiated tolerability profile compared to current and emerging therapies.

在優化的RP2D下治療的所有腫瘤類型中(n=67),Lunre+Camo治療顯示出與當前和新興療法相比,良好且有區別的耐受性特徵。

The most common adverse event was anemia (26.9%, Grade 3).

最常見的不良事件是貧血(26.9%,3級)。

Key Cohort Clinical Findings

關鍵隊列臨床發現

Key efficacy outcomes from 27 evaluable patients with endometrial cancer show:

27名可評估的子宮內膜癌患者的關鍵療效結果顯示:

  • Overall response rate was 25.9% (confirmed ORR in 5 out of 7 patients).
  • Clinical benefit was observed in 48.1% of patients, with responses frequently occurring after 12 weeks or more.
  • At the 24-week landmark analysis, nearly half of patients experienced durable clinical benefit (24-week PFS [PFS24w] = 43%.
  • 總體反應率爲25.9%(在7名患者中確認的ORR爲5名)。
  • 48.1%的患者觀察到臨床益處,反應通常在12周或更長時間後發生。
  • 在24周的里程碑分析中,近一半的患者經歷了持久的臨床獲益(24周無進展生存期[PFS24w] = 43%)。

Key efficacy outcomes in 24 evaluable Platinum-Resistant Ovarian Cancer patients show:

在24例可評估的鉑金耐藥性卵巢癌患者中,關鍵療效結果顯示:

  • Overall response rate was 37.5% (confirmed ORR in 4 out of 9 patients).
  • Clinical benefit was observed in 79% of patients.
  • PFS at the 24-week landmark analysis was PFS24w = 45%.
  • 總體反應率爲37.5%(在9名患者中確認的ORR爲4名)。
  • 在79%的患者中觀察到臨床獲益。
  • 在24周的里程碑分析中,PFS爲PFS24w = 45%。

Repare has consulted with the FDA and the European Medicines Agency, who have guided the company's registrational development plans for Lunre+Camo in gynecologic tumors.

Repare已與FDA和歐洲藥品管理局進行諮詢,這些機構指導公司在婦科腫瘤領域的註冊開發計劃。

Repare plans to provide the final Phase 3 trial protocols for regulatory clearance imminently and intends to start the first Phase 3 Lunre+Camo trial in endometrial cancer in the second half of 2025.

Repare計劃儘快提供最終的第三期臨床試驗方案以獲得監管批准, 並打算在2025年下半年開始首次的第三期Lunre+Camo試驗,針對子宮內膜癌。

Additionally, the company expects to initiate a small contribution of components trial in up to 40 patients with endometrial cancer in the first quarter of 2025.

此外,公司預計將在2025年第一季度啓動一個針對多達40名子宮內膜癌患者的小規模元件試驗。

Price Action: RPTX stock is down 52.4% at $1.89 at last check Friday.

價格走勢:RPTX 股票在最後一次檢查時下跌了52.4%,目前價格爲1.89美元。

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Photo via Shutterstock.

圖片來自shutterstock。

譯文內容由第三人軟體翻譯。


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