BENITIONSClinical Trial Intelligence

Perioperative Pembrolizumab (MK-3475) Plus Cystectomy or Perioperative Pembrolizumab Plus Enfortumab Vedotin Plus Cystectomy Versus Cystectomy Alone in Participants Who Are Cisplatin-ineligible or Decline Cisplatin With Muscle-invasive Bladder Cancer (MK-3475-905/KEYNOTE-905/EV-303)

Фаза 3 Идёт, набор закрыт NCT03924895

ЗаболеваниеUrinary Bladder Cancer, Muscle-invasive
ФазаФаза 3
СпонсорMerck Sharp & Dohme LLC
СтатусИдёт, набор закрыт
Участники595 участн.
ВмешательствоPembrolizumab, Surgery (radical cystectomy (RC) plus Pelvic Lymph Node Dissection [PLND]), Enfortumab Vedotin
Дата начала24.07.2019
Дата завершения6.06.2025
Публикация результатов30.06.2026

Кратко

This is a study of perioperative pembrolizumab or enfortumab vedotin in combination with pembrolizumab in participants who are cisplatin-ineligible or decline cisplatin with muscle-invasive bladder cancer (MIBC). The primary hypothesis is that perioperative pembrolizumab plus radical cystectomy (RC) plus pelvic lymph node dissection (PLND) and perioperative enfortumab vedotin in combination with pembrolizumab plus RC+PLND will achieve superior event-free survival (EFS) compared with RC+PLND alone. With Amendment 5, outcome measures for programmed cell death ligand 1 (PD-L1) combined positive score (CPS) were removed. With Amendment 8, the primary outcome measure of pathologic complete response (pCR) rates was changed to a secondary outcome measure.

Event-Free Survival (EFS) Between Arm C: Enfortumab Vedotin + Pembrolizumab + Surgery and Arm B: Surgery Alone

Up to approximately 53 months · Months

Arm B: Surgery Alone15.7 Months
Arm C: Enfortumab Vedotin + Pembrolizumab + SurgeryNA Months
p-value<0.0001
Hazard Ratio (HR)0.40 (95% CI 0.28–0.57)

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