OncoMatch

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.

Phase 2RecruitingMerck Sharp & Dohme LLCNCT04924075Data as of May 2026

Treatment: BelzutifanThis 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 qualify

Extracted 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 →

Could you qualify for this trial?

Enter your biomarker results to see how this trial's eligibility criteria match your specific cancer profile.

Check if I qualify