Real-World Effectiveness and Pharmacogenetics of Belzutifan in VHL Syndrome: The BELIEVE-VHL Trial (NCT07167329) | Clinical Trial Compass
RecruitingPhase 2
Real-World Effectiveness and Pharmacogenetics of Belzutifan in VHL Syndrome: The BELIEVE-VHL Trial
Brazil100 participantsStarted 2024-01-01
Plain-language summary
The BELIEVE-VHL Trial is a prospective real-life study designed to evaluate the therapeutic effects, benefits, and adverse effects of belzutifan, as well as the timing of treatment response and disease progression in patients with von Hippel-Lindau (VHL) syndrome.
Who can participate
Age range14 Years
SexALL
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Inclusion Criteria:
* Age ≥ 14 years.
* Clinical or genetic confirmation of von Hippel-Lindau (VHL) syndrome.
* Presence of measurable or progressive VHL-associated tumors, as defined by RECIST 1.1 or disease-specific imaging criteria.
* ECOG performance status of 0-2.
* Adequate bone marrow, hepatic, and renal function as defined by laboratory reference values.
* Ability to swallow oral medication.
* Provision of written informed consent prior to enrollment.
Exclusion Criteria:
* Age \< 14 years.
* Absence of a confirmed diagnosis of von Hippel-Lindau (VHL) syndrome.
* Presence of an active malignancy outside the VHL tumor spectrum within the past 3 years, except for adequately treated basal or squamous cell carcinoma of the skin, cervical carcinoma in situ, or other malignancies considered cured for \>2 years.
* Known hypersensitivity or allergic reaction to belzutifan or any excipient in the formulation.
* History of severe or uncontrolled cardiovascular disease, including but not limited to unstable angina, myocardial infarction within the past 6 months, congestive heart failure requiring treatment, or uncontrolled hypertension.
* Active infectious diseases, including HIV, hepatitis B, or hepatitis C.
* Immunosuppressed status, whether due to underlying disease or ongoing therapy.
* History of significant bleeding disorders, including bleeding diathesis, thrombocytopenia, or coagulopathy.
* Radiotherapy administered within 4 weeks prior to study enrollment.
* Major sur…
What they're measuring
1
Objective Tumor Response per RECIST 1.1
Timeframe: From enrollment and initiation of treatment until the earliest of either documented disease progression or death from any cause, with follow-up of up to 104 weeks.