熱門資訊> 正文
Reported Saturday, Genmab's Rinatabart Sesutecan Achieves 50% Objective Response Rate And Two Complete Responses In Advanced Endometrial Cancer; Phase 3 Trial And US FDA Breakthrough Therapy Designation Underway
2025-10-20 16:08
- Updated data from the Phase 1/2 RAINFOL™-01 trial showed rinatabart sesutecan (Rina-S®) 100 mg/m2 demonstrated 50% confirmed objective response rate (ORR), including two complete responses (CR), regardless of FRα expression
- A Phase 3 trial in endometrial cancer is underway
- U.S. FDA recently granted Breakthrough Therapy Designation to Rina-S for advanced endometrial cancer
風險及免責提示:以上內容僅代表作者的個人立場和觀點,不代表華盛的任何立場,華盛亦無法證實上述內容的真實性、準確性和原創性。投資者在做出任何投資決定前,應結合自身情況,考慮投資產品的風險。必要時,請諮詢專業投資顧問的意見。華盛不提供任何投資建議,對此亦不做任何承諾和保證。