drugset / Trial / NCT00225121

Study To Evaluate The Safety, Pharmacokinetics, And Pharmacodynamics Of PF-00299804 In Patients With Advanced Solid Tumors

NCT00225121

Phase 1 Completed 121 enrolled Pfizer
Open-labelTreatment

Summary

The primary purpose of this study is to study the side effects of PF-00299804 and determine the highest dose that can be safely administered in patients with advanced cancer.

Timeline

Start
2005-10-11
Primary completion
2007-04-03
Completion
2010-09-23

Drugs

EvaluationDrugModalityDoseRoute
Subject DACOMITINIB ANHYDROUS Small molecule 45 mg Oral

Indications