New hope for rare genetic tumor disorder: belzutifan trial launches
NCT ID NCT07167329
First seen Nov 01, 2025 · Last updated May 25, 2026 · Updated 34 times
Summary
This study is for people with von Hippel-Lindau (VHL) syndrome, a rare genetic condition that causes tumors in various organs. Researchers want to see how well the drug belzutifan works at shrinking or controlling these tumors, and what side effects it may cause. About 100 participants aged 14 and older will be followed for up to two years. The goal is to better understand how this medication can help manage the disease over time.
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Summaries may miss details or leave out important information. Before applying or accepting participation, make sure you have read and understood the full study. Curemydisease.com takes no responsibility whatsoever for anything missed, misunderstood, or acted upon as a result of our summary — we know it does not capture everything.
This is a summary of the original study . Summaries may miss details or leave out important information. Before applying or accepting participation, make sure you have read and understood the full study. Curemydisease.com takes no responsibility whatsoever for anything missed, misunderstood, or acted upon as a result of our summary — we know it does not capture everything.
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Locations
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AC Camargo Cancer Center
RECRUITINGSão Paulo, São Paulo, 01509900, Brazil
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Conditions
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