OncoMatch/Clinical Trials/NCT04924075
Belzutifan/MK-6482 for the Treatment of Advanced Pheochromocytoma/Paraganglioma (PPGL), Pancreatic Neuroendocrine Tumor (pNET), Von Hippel-Lindau (VHL) Disease-Associated Tumors, Advanced Gastrointestinal Stromal Tumor (wt GIST), or Solid Tumors With HIF-2α Related Genetic Alterations (MK-6482-015)
Is NCT04924075 recruiting? Yes, currently enrolling (May 2026). This Phase 2 trial studies Belzutifan for pheochromocytoma/paraganglioma.
Treatment: Belzutifan — This is a study to evaluate the efficacy and safety of belzutifan monotherapy in participants with advanced pheochromocytoma/paraganglioma (PPGL), pancreatic neuroendocrine tumor (pNET), von Hippel-Lindau (VHL) disease-associated tumors, advanced wt (wild-type) gastrointestinal stromal tumor (wt GIST), or advanced solid tumors with hypoxia inducible factor-2 alpha (HIF-2α) related genetic alterations. The primary objective of the study is to evaluate the objective response rate (ORR) of belzutifan per response evaluation criteria in solid tumors version 1.1 (RECIST 1.1) by blinded independent central review (BICR).
Check if I qualifyExtracted eligibility criteria
Cancer type
Neuroendocrine Tumor
Gastrointestinal Stromal Tumor
Biomarker criteria
Required: EPAS1 any mutation
advanced solid tumors with Hypoxia Inducible Factor- 2 alpha subunit (HIF-2α) related genetic alterations
Required: VHL any mutation
diagnosis of VHL disease as determined by a germline test locally and/or clinical diagnosis
Disease stage
Required: Stage IV, LOCALIZED (VHL DISEASE-ASSOCIATED TUMORS)
Advanced/metastatic... or VHL disease associated localized tumors
Prior therapy
Cannot have received: chemotherapy
Exception: somatostatin analogs
Received prior treatment (except somatostatin analogs) with chemotherapy, targeted therapy, biologics, or other investigational therapy within the past 4 weeks of first dose of study intervention
Cannot have received: targeted therapy
Exception: somatostatin analogs
Received prior treatment (except somatostatin analogs) with chemotherapy, targeted therapy, biologics, or other investigational therapy within the past 4 weeks of first dose of study intervention
Cannot have received: biologics
Exception: somatostatin analogs
Received prior treatment (except somatostatin analogs) with chemotherapy, targeted therapy, biologics, or other investigational therapy within the past 4 weeks of first dose of study intervention
Cannot have received: other investigational therapy
Exception: somatostatin analogs
Received prior treatment (except somatostatin analogs) with chemotherapy, targeted therapy, biologics, or other investigational therapy within the past 4 weeks of first dose of study intervention
Structured fields extracted by AI. May contain errors — verify against the official protocol.
US trial sites
- Cedars-Sinai Medical Center ( Site 0110) · Los Angeles, California
- Northwestern University - Robert H. Lurie Comprehensive Cancer Center ( Site 0130) · Chicago, Illinois
- Northwestern Medicine Cancer Center - Warrenville ( Site 0134) · Warrenville, Illinois
- University of Iowa ( Site 0104) · Iowa City, Iowa
- Johns Hopkins Hospital-Sidney Kimmel Comprehensive Cancer Center - Developmental Therapeutics ( Site 0108) · Baltimore, Maryland
Showing up to 5 US sites. See all sites on ClinicalTrials.gov →
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