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Extension Study for Participants in Studies That Include Belzutifan (MK-6482-043/LITESPARK-043)

RecruitingPhase 3

A Multicenter, Open-label, Phase 3 Extension Study to Evaluate the Long-term Efficacy and Safety in Participants Who Are Currently on Treatment in a Belzutifan Study (LITESPARK-043)

Who can join

Ages 18 and older · All sexes

Full eligibility criteria
Inclusion Criteria:

The main inclusion criteria include but are not limited to the following:

* Participants with advanced solid tumors or von Hippel-Lindau-related neoplasms who are participating in belzutifan-containing studies and on active treatment in a belzutifan parent study.

Exclusion Criteria:

The main exclusion criteria include but are not limited to the following:

* Has an on-going serious adverse event in the parent study, unless no longer hospitalized and considered clinically stable.
* Is currently on a dose interruption due to an Adverse Event (AE) in the parent study; once treatment has been resumed in the parent study, the participant is eligible to enroll.

About the study

Researchers are looking for new ways to treat advanced solid tumors and von Hippel-Lindau (VHL)-related tumors:

* Advanced means the cancer has spread to other parts of the body (metastatic) or cannot be removed with surgery * Solid tumors are cancers mostly in body organs and tissues, not in the blood or other body liquids * VHL-related tumors are tumors caused by VHL disease. VHL disease is passed down from parents to children and people with VHL disease have a higher chance of getting certain types of cancer

Researchers want to learn about the long-term effects of a trial medicine called belzutifan. Belzutifan, also called MK-6482, is designed to block a protein that helps tumors grow and survive. This is an extension trial, which means only people who were in certain other belzutifan trials (called parent trials) may be able to join. The goal of this trial is to learn how long people live after they start taking belzutifan.

What is being tested

Sponsor: Merck Sharp & Dohme LLC · Participants: 450 · Started: Mar 23, 2026

Contact the study team

Official record on ClinicalTrials.gov — NCT07405164

Locations in the U.S.

MassachusettsBeth Israel Deaconess Medical Center ( Site 0107), Boston
Dana-Farber Cancer Institute ( Site 0105), Boston
MichiganKarmanos Cancer Center ( Site 0108), Detroit
PennsylvaniaHospital of the University of Pennsylvania Perelman Center for Advanced Medicine ( Site 0100), Philadelphia
TennesseeSCRI Oncology Partners ( Site 7000), Nashville
TexasSTART San Antonio ( Site 0104), San Antonio
WashingtonFred Hutchinson Cancer Center ( Site 0106), Seattle

Conditions

From ClinicalTrials.gov, data retrieved Sep 30, 2026. Each study sets its own eligibility; the study team decides who can join.