A Study of GV20-0251 in Advanced or Refractory Solid Tumors
Single Arm Clinical Study Protocol of GV20-0251 in the Treatment of Advanced/Refractory Solid Tumors
West China Hospital
10 participants
Sep 4, 2025
INTERVENTIONAL
Conditions
Summary
This is a single-arm, single-center study for multiple tumor indications to evaluate the safety of GV20-0251. The trial uses a 3 + 3 design and enrolls 3-6 patients in the 10 mg/kg and 20 mg/kg dose groups, respectively. The cancer types include solid tumors.
Eligibility
Plain Language Summary
Simplified for easier understanding
This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.
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Interventions
Increasing doses of GV20-0251 administered by intravenous (IV) infusion once every 3 weeks
Locations(1)
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NCT07106827