drugset / Trial / NCT00615446

A Study To Find The Best Doses Of SU011248 And Gemcitabine When Given Together To Patients With Advanced Solid Tumors

NCT00615446

Phase 1 Completed 44 enrolled Pfizer
Non-randomizedParallel-groupOpen-labelTreatment

Summary

This study assesses the maximum tolerated dose, overall safety and antitumor activity of SU011248 in combination with gemcitabine in patients with advanced solid tumors

Timeline

Start
2005-03
Primary completion
2009-05
Completion
2009-05

Drugs

EvaluationDrugModalityDoseRoute
Subject Gemcitabine Small molecule 750 mg/m2 Intravenous
Subject Gemcitabine Small molecule 1250 mg/m2 Intravenous
Subject Sunitinib Small molecule 25 mg Oral
Subject Sunitinib Small molecule 50 mg Oral

Indications