CEL-SCI Announced Multikine Demonstrates Tumor Regression Pre-Surgery In 3 Weeks; FDA Approves 212-Person Study With 73% Survival Rate Vs. 45% Control In Head And Neck Cancer
CEL-SCI Announced Multikine Demonstrates Tumor Regression Pre-Surgery In 3 Weeks; FDA Approves 212-Person Study With 73% Survival Rate Vs. 45% Control In Head And Neck Cancer
CEL-SCI宣佈Multikine在手術前3周內顯示腫瘤縮小;FDA批准212人研究,73%的生存率對比頭頸癌控制組的45%。
- Multikine is the first cancer immunotherapy to show pre-surgical tumor regression in head and neck cancer in just 3 weeks - confirmed by pathology at surgery
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Factors supporting the go-ahead for the 212-person registration study in the target population include:
- Multikine led to significant rates of tumor regression
- Pre-surgical tumor regressions were confirmed at surgery and forecast survival benefit
- Target population is likely to show significant survival prolongation in the confirmatory study
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Confirmatory study target population selection is based on:
- Strong statistical significance in a large subgroup of 114 patients
- Subgroup analysis was pre-defined in the statistical analysis plan (SAP)
- Strong biological rationale for the results based on Multikine's mechanism of action (MOA)
- Multikine是首個在頭頸癌患者中展示術前腫瘤退縮的癌症免疫治療,且僅需3周時間 - 由手術病理確認
- 支持在目標人群中進行212人註冊研究的因素包括:
- Multikine導致了顯著的腫瘤退縮率
- 術前腫瘤退縮在手術中得到了確認,並預計將帶來生存益處
- 目標人群在確認研究中可能會顯示出顯著的生存延長
- 確認研究的目標人群選擇基於:
- 在114名患者的大分組中顯示出了強統計學意義
- 分組分析是在統計分析計劃(SAP)中預先定義的
- 基於Multikine的作用機理,結果具有強大的生物學合理性
CEL-SCI Corporation (NYSE:CVM) today highlights strong biological rationale for the use of Multikine in the confirmatory registration head and neck cancer study. This study of 212 newly diagnosed locally advanced, resectable head and neck cancer patients was given the go-ahead as a confirmatory registration study by FDA and will focus on those patients who showed a 73% survival with Multikine vs. a 45% for the control patients not treated with Multikine in the prior Phase 3 study.
CEL-SCI公司(紐交所:CVM)今天強調了在確認註冊頭頸癌研究中使用Multikine的強大生物學合理性。這項涉及212名新診斷的局部晚期、可切除頭頸癌患者的研究,已獲得FDA批准作爲確認註冊研究,將重點關注在之前的第3期研究中顯示使用Multikine患者的73%生存率對比未治療Multikine的對照組患者的45%。
譯文內容由第三人軟體翻譯。
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