Pure Global AI
NCT06307431Recruiting

A Study of Adjuvant V940 and Pembrolizumab in Renal Cell Carcinoma (V940-004)

A Phase 2, Randomized, Double-blind, Clinical Study of V940 (mRNA-4157) Plus Pembrolizumab (MK-3475) Versus Placebo Plus Pembrolizumab in the Adjuvant Treatment of Participants With Renal Cell Carcinoma
Merck Sharp & Dohme LLCPhase 2ClinicalTrials.govbiological
Study focus
Disease/Condition
Renal Cell Carcinoma
Drug/Device/Intervention
V940
Study type
Interventional
Intervention type
biological
Sponsor & location
Primary sponsor
Merck Sharp & Dohme LLC
Location
New Haven,New York,Macquarie University,Québec,Santiago,Santiago,Santiago,Viña del Mar,Taipei, Australia,Canada,Chile,Taiwan,United States of America
Timeline & enrollment
Phase
Phase 2
Start date
Apr 10, 2024
End date
Jun 08, 2032
Enrollment
272 participants
Primary outcome

Disease-Free Survival (DFS)

Summary

The primary objective of the study is to compare V940 plus pembrolizumab to placebo plus
 pembrolizumab with respect to disease-free survival (DFS) as assessed by the investigator.
 The primary hypothesis is that V940 plus pembrolizumab is superior to placebo plus
 pembrolizumab with respect to DFS.

ICD-10 classifications
Malignant neoplasm of kidney, except renal pelvisMalignant neoplasm of renal pelvisSecondary malignant neoplasm of kidney and renal pelvisBenign neoplasm: KidneyBenign neoplasm: Renal pelvis
Data source
Registry
ClinicalTrials.gov
Trial ID
NCT06307431
Type
Non-Device Trial
About this record

Access comprehensive clinical trial information for NCT06307431 through Pure Global AI's free database. This Phase 2 trial is sponsored by Merck Sharp & Dohme LLC and is currently Recruiting. The study focuses on Renal Cell Carcinoma. Target enrollment is 272 participants.

This page provides complete trial specifications, intervention details, outcomes, and location information. Pure Global AI offers free access to ClinicalTrials.gov data, helping medical device and pharmaceutical companies navigate clinical research efficiently.