drugset / Trial / NCT06222593

Study to Evaluate the Safety and Efficacy of Bicalutamide in Combination With Sunitinib in Patients With TKIs-resistant RCC

NCT06222593

Phase 1/2 Recruiting 28 enrolled State University of New York at Buffalo
NaSingle-groupOpen-labelTreatment

Summary

This is a Phase I/II open-label, efficacy and safety study of bicalutamide in combination with sunitinib in patients with advanced renal cell carcinoma (RCC) who have been treated with a receptor tyrosine kinase inhibitor (RTKI) and experienced disease progression.

Timeline

Start
2024-10-01
Primary completion
2026-07-01
Completion
2027-07-01

Drugs

EvaluationDrugModalityDoseRoute
Subject Bicalutamide Other / unclassified 50 mg Oral
Subject Sunitinib Small molecule 25 mg
Subject Sunitinib Small molecule 37.5 mg
Subject Sunitinib Small molecule 50 mg

Indications