MK-7684A
Sponsors
Merck Sharp & Dohme LLC
Conditions
Advanced solid tumorsExtensive-stage small-cell lung cancerMetastatic Castration-Resistant Prostate CancerMetastatic Non-Small Cell Lung CancerNon Small Cell Lung cancerNon-Muscle Invasive Bladder Cancer (NMIBC)Non-small cell lung cancerParticipants with Microsatellite Instability-High (MSI-H) or Mismatch Repair Deficient (dMMR) Stage IV Colorectal Cancer
Phase 1
A Phase 1b/2 Study of Immune and Targeted Combination Therapies in Participants with RCC (KEYMAKER-U03): Substudy 03A in First Line Metastatic Participants
RecruitingCTIS2023-506838-68-00
Start: 2020-12-10Target: 62Updated: 2025-11-07
Phase Ib/II Trial of Pembrolizumab (MK-3475) Combination Therapies in Metastatic Castration-Resistant Prostate Cancer (mCRPC) (KEYNOTE-365)
RecruitingCTIS2023-506987-15-00
Start: 2016-11-17Target: 294Updated: 2025-11-03
Phase 2
A Phase 2, Multicenter, Randomized Study to Compare the Efficacy and Safety of MK-7684A or MK-7684A Plus Docetaxel Versus Docetaxel Monotherapy in the Treatment of Participants With Metastatic Non-small Cell Lung Cancer With Progressive Disease After Treatment With a Platinum Doublet Chemotherapy and Immunotherapy
CompletedCTIS2022-501252-28-00
Start: 2021-04-15End: 2024-10-10Target: 150Updated: 2024-11-25
A Phase II Clinical Trial to Study the Efficacy and Safety of Pembrolizumab (MK-3475) and Pembrolizumab in Combination with Other Investigational Agents in Subjects with High-risk Non-muscle-Invasive Bladder Cancer (NMIBC) Unresponsive to Bacillus Calmette-Guerin (BCG) Therapy
CompletedCTIS2022-502526-41-00
Start: 2016-03-15End: 2025-11-05Target: 102Updated: 2025-09-08
A Phase 2, Multicenter, Multi Arm, Study to Evaluate MK-1308A (Coformulated quavonlimab (MK-1308)/pembrolizumab) Versus Other Treatments in Participants with Microsatellite Instability-High (MSI-H) or Mismatch Repair Deficient (dMMR) Stage IV Colorectal Cancer: (MK-1308A-008)
Active, not recruitingCTIS2022-502100-70-00
Start: 2021-06-23Target: 244Updated: 2026-01-27
A Multicenter, Open-label, Phase 2 Basket Study of MK‑7684A, a Co formation of Vibostolimab (MK‑7684) With Pembrolizumab (MK‑3475), With or Without Other Anticancer Therapies in Participants With Selected Solid Tumors (KEYVIBE 005)
CompletedCTIS2023-505284-36-00
Start: 2021-09-13End: 2025-06-27Target: 228Updated: 2025-07-01
Phase 3
A Phase 3, Randomized, Double-blind, Active-Comparator-Controlled Clinical Study of Adjuvant MK-7684A (Vibostolimab with Pembrolizumab) Versus Adjuvant Pembrolizumab in Participants with High-risk Stage II-IV Melanoma (KEYVIBE-010)
CompletedCTIS2022-501417-31-01
Start: 2023-08-01End: 2025-09-04Target: 462Updated: 2025-08-20
A Phase 3, Randomized, Double-Blind Study of MK-7684A in Combination with Etoposide and Platinum Followed by MK-7684A vs Atezolizumab in Combination with Etoposide and Platinum Followed by Atezolizumab for the First-Line Treatment of Participants with Extensive-Stage Small Cell Lung Cancer (KEYVIBE-008)
Active, not recruitingCTIS2023-503517-30-00
Start: 2022-04-01Target: 256Updated: 2025-11-20
Open-label Phase 3 Study of MK-7684A (Coformulation of Vibostolimab with Pembrolizumab) in Combination with Concurrent Chemoradiotherapy followed by MK7684A Versus Concurrent Chemoradiotherapy followed by Durvalumab in Participants with Unresectable, Locally Advanced, Stage III NSCLC (KEYVIBE-006)
RecruitingCTIS2022-502752-31-00
Start: 2022-04-29Target: 68Updated: 2025-12-11
A Randomized, Double-Blind, Phase 3 Study of Pembrolizumab/Vibostolimab Coformulation (MK-7684A) in Combination with Chemotherapy Versus Pembrolizumab Plus Chemotherapy as First Line Treatment for Participants with Metastatic Non-Small Cell Lung Cancer (MK-7684A-007/KEYVIBE-007)
CompletedCTIS2023-506074-12-00
Start: 2022-03-22End: 2025-12-23Target: 190Updated: 2025-12-23
A Phase 3, Multicenter, Randomized, Double-Blind Study of MK-7684 with Pembrolizumab as a Coformulation (MK-7684A) Versus Pembrolizumab Monotherapy as First Line Treatment for Participants With PD-L1 Positive Metastatic Non-Small Cell Lung Cancer (KEYVIBE-003)
CompletedCTIS2023-505362-28-00
Start: 2021-04-21End: 2026-01-20Target: 156Updated: 2025-09-02