CLINICAL TRIALS PROFILE FOR MK-6482
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Clinical Trials for MK-6482
Trial ID | Title | Status | Sponsor | Phase | Summary |
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NCT02974738 ↗ | A Trial of Belzutifan (PT2977, MK-6482) Tablets In Patients With Advanced Solid Tumors (MK-6482-001) | Active, not recruiting | Peloton Therapeutics, Inc. | Phase 1 | The primary objective of this study is to identify the maximum tolerated dose (MTD) of belzutifan Tablets and/or the recommended Phase 2 dose (RP2D) of belzutifan Tablets in patients with advanced solid tumors |
NCT03401788 ↗ | A Phase 2 Study of Belzutifan (PT2977, MK-6482) for the Treatment of Von Hippel Lindau (VHL) Disease-Associated Renal Cell Carcinoma (RCC) (MK-6482-004) | Active, not recruiting | Peloton Therapeutics, Inc. | Phase 2 | This study is designed to investigate belzutifan as a treatment for VHL disease associated RCC. |
NCT03445169 ↗ | A Food Effect Study in Healthy Volunteers With Belzutifan (PT2977, MK-6482) Tablets | Completed | Peloton Therapeutics, Inc. | Phase 1 | This Phase 1, single-dose study will be conducted in adult male and female subjects (N = 16) who are in general good health and selected for participation in the study according to the selection criteria. This study will assess the effect of food on the pharmacokinetics of belzutifan Tablets. The study will consist of two periods and will be conducted in a crossover fashion. |
NCT03634540 ↗ | A Trial of Belzutifan (PT2977, MK-6482) in Combination With Cabozantinib in Patients With Clear Cell Renal Cell Carcinoma (ccRCC) (MK-6482-003) | Recruiting | Peloton Therapeutics, Inc. | Phase 2 | This is an open-label Phase 2 study which will evaluate the efficacy and safety of belzutifan in combination with cabozantinib in participants with advanced ccRCC. Belzutifan and cabozantinib will be administered orally once daily. |
NCT04195750 ↗ | A Study of Belzutifan (MK-6482) Versus Everolimus in Participants With Advanced Renal Cell Carcinoma (MK-6482-005) | Recruiting | Merck Sharp & Dohme Corp. | Phase 3 | The primary objective of this study is to compare belzutifan to everolimus with respect to progression-free survival (PFS) per Response Evaluation Criteria in Solid Tumors Version 1.1 (RECIST 1.1) as assessed by Blinded Independent Central Review (BICR) and to compare everolimus with respect to overall survival (OS). The hypothesis is that belzutifan is superior to everolimus with respect to PFS and OS. |
>Trial ID | >Title | >Status | >Sponsor | >Phase | >Summary |
Clinical Trial Conditions for MK-6482
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Clinical Trial Sponsors for MK-6482
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