drugset / Trial / NCT00113529

Study Of SU011248 Plus Gefitinib (Iressa) In Patients With Advanced Renal Cell Carcinoma

NCT00113529

Phase 1/2 Completed 42 enrolled Pfizer
Non-randomizedSingle-groupOpen-labelTreatment

Summary

To assess the maximum tolerated dose and overall safety and tolerability of sunitinib \[SU011248\] administered in combination with gefitinib (Iressa) for the treatment of patients with metastatic renal cell carcinoma (Phase 1). To assess antitumor activity of the combination of gefitinib and sunitinib (Phase 2).

Timeline

Start
2004-10
Primary completion
2007-09
Completion
2008-10

Drugs

EvaluationDrugModalityDoseRoute
Subject Gefitinib Small molecule 250 mg
Subject Sunitinib Small molecule 37.5 mg Oral
Subject Sunitinib Small molecule 50 mg Oral

Indications