drugset / Trial / NCT00247676

An International Phase 2 Study Of SU011248 In Patients With Inoperable Liver Cancer

NCT00247676 ↗

Phase 2 Completed 37 enrolled Pfizer
Non-randomizedSingle-groupOpen-labelTreatment

Summary

The study will consist of two parts. In Part 1 the study will start enrolling 38 patients and then further 25 patients up to a total of 63 eligible patients. If the study gives good results it can be expanded to a total of 160 patients. SU011248 will be administered orally daily for 4 weeks followed by a 2-week rest at a starting dose of 50 mg \[milligrams\] with provision for dose reduction based on tolerability. All patients will receive repeated cycles of SU011248 until disease progression, occurrence of unacceptable toxicity, or other withdrawal criteria are met. After discontinuation of treatment, patients will be followed up in order to collect information on further antineoplastic therapy and survival

Timeline

Start
2006-02
Primary completion
2008-02
Completion
2009-02

Outcome

Missed primary endpoint

paper the study did not meet the primary endpoint based on RECIST criteria. PMID 19586800 ↗

Drugs

EvaluationDrugModalityDoseRoute
Subject Sunitinib Small molecule 50 mg Oral