Frontlight ResearchEarly access
Taking people in DenmarkPhase 3
Long-term belzutifan treatment for adults with solid tumors or von Hippel-Lindau disease tumors
Continues belzutifan for adults with solid tumors or von Hippel-Lindau-related tumors.
Key facts
- Who runs it
- Merck Sharp & Dohme LLC
- Where
- Herlev, DenmarkSee the siteAlso in 9 other countries, 23 sites
- Trial code
- EU 2025-524160-38-00
- U1111-1325-4582
- Registry title
- A clinical trial of belzutifan and other treatments in people with solid tumors or von Hippel-Lindau (VHL)-related tumors (MK-6482-043)
- Status
- Recruiting
- Phase
- Phase 3
- People taking part
- 134 people, planned
- Started
- 12 May 2026
- Expected to end
- 30 Jun 2034
- Type of study
- Interventional
- Record updated
- 11 November 2026
Who can take part
AI summary
From the trial's eligibility criteria. Machine-read from the registry text on this page, so it can be wrong. The registry text below and the trial team decide who can take part.
The trial is looking for adults with advanced solid tumors or von Hippel-Lindau-related tumors who are on active treatment in a belzutifan study and want to continue.
- Age
- 18 years or older
- Sex
- All sexes can join.
- Disease stage
- Advanced solid tumors or von Hippel-Lindau-related tumors.
- Earlier treatment
- Must be on active treatment in a belzutifan parent study.
Main reasons for not taking part
- An ongoing serious adverse event in the parent study, unless no longer hospitalized and clinically stable
- Currently on a dose interruption because of an adverse event in the parent study
The registry criteria, word for word
Show all 3 criteriaShow less
Who can take part
- 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
Who cannot take part
- 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
- Has an on-going serious adverse event in the parent study, unless no longer hospitalized and considered clinically stable
Check if you might fit
Answer for yourself. This is not a decision: only the study team can say whether you can take part.
- Are you 18 years old or older?
Where in Denmark
Also in 9 other countries, 23 sites
- Region HovedstadenHerlev, DenmarkTaking people
About the trial
What the trial wants to find out
To assess OS in Cohort A and Cohort B
Questions to ask the study team
- How often do I need to come in, and for how long each time?
- Are travel costs paid?
- Can I keep my own doctor?
- What happens if I want to stop?
Contact the study team: see the registry record
Print a page for my doctorData and sources
- Registry record
- Listed on the EU's official list of trials (CTIS).
- Official title
- 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)
- Plain-language title
- Long-term belzutifan treatment for adults with solid tumors or von Hippel-Lindau disease tumorsGenerated from the registry record. The registry title is the official one.
- AI summary
- From the trial's eligibility criteria. Read by machine on 12 November 2026.
- Fit questions
- Built from 2025-524160-38-00, who can take part
- Record updated
- 11 November 2026