Metronomic Gemcitabine, Mitomycin C, and Thalidomide for Advanced Solid Tumors
GEMINI: Phase II Study Using Metronomic Gemcitabine, Mitomycin C, and Thalidomide for Advanced Solid Tumors
Sarcoma Oncology Research Center, LLC
60 participants
Jun 1, 2026
INTERVENTIONAL
Conditions
Summary
This is an open label phase II study using metronomic low-dose gemcitabine and mitomycin c given intravenously, and thalidomide administered orally, for patients with advanced 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
600 mg/m2 (Max: 1000 mg) i.v. on D1, D8, D15
Mitomycin C 14 mg i.v. every 6 weeks
Thalidomide 100 mg daily x 15 days
Locations(1)
View Full Details on ClinicalTrials.gov
For the most up-to-date information, visit the official listing.
NCT07671534