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

Part of paid clinical trials in Duarte, California.

Sponsor
Merck Sharp & Dohme LLC
Study ID
NCT06307431
Phase
PHASE2
Status
Active Not Recruiting

Conditions

Eligibility Criteria

Sex
ALL
Age
18 Years - N/A
Healthy Volunteers
Not accepted

Interventions

  • Intismeran autogene — BIOLOGICAL
    IM injection
  • Pembrolizumab — BIOLOGICAL
    IV infusion
  • Placebo — BIOLOGICAL
    IM injection

Study Details

The primary objective of the study is to compare intismeran autogene plus pembrolizumab to placebo plus pembrolizumab in participants with renal cell carcinoma (RCC) with respect to disease-free survival (DFS) as assessed by the investigator. The primary hypothesis is that intismeran autogene plus pembrolizumab is superior to placebo plus pembrolizumab with respect to DFS.

Key Dates

Start date
Apr 10, 2024
Status verified
Aug 2025
Primary completion
Jan 8, 2028
Completion
Jun 8, 2032

Study Design

Enrollment
272 participants (estimated)
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT

Arms

  • Experimental: Intismeran autogene + Pembrolizumab
    Participants will receive intismeran autogene 1 mg via intramuscular (IM) injection every 3 weeks (Q3W) for up to 9 doses plus Pembrolizumab 400 mg via an intravenous (IV) infusion every 6 weeks (Q6W) for 9 cycles (up to \~54 weeks). Each cycle is 6 weeks.
  • Active Comparator: Placebo + Pembrolizumab
    Participants will receive placebo as an IM injection Q3W for up to 9 doses plus Pembrolizumab 400 mg via an IV infusion Q6W for 9 cycles (up to \~54 weeks). Each cycle is 6 weeks.

Primary Outcome Measure

Disease-Free Survival (DFS) [ Time Frame: up to ~43 months ]

Locations (11)

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