drugset / Trial / NCT01147809

Safety and Efficacy Study for Solid Tumor Patients Treated With Eltrombopag

NCT01147809

Phase 2 Completed 130 enrolled GlaxoSmithKline
RandomizedParallel-groupDouble-blindSupportive care

Summary

The present study is a randomized, blinded, placebo-controlled, two-Phase, sequential cohort, dose finding study to assess the safety and efficacy of eltrombopag in patients with solid tumors receiving gemcitabine monotherapy or the combination of gemcitabine plus carboplatin or cisplatin. Phase I of the study will examine safety and tolerability of various doses of eltrombopag to identify a dose and schedule of eltrombopag. Phase II will confirm that the chosen dose and schedule of eltrombopag from Phase I can deliver clinically meaningful benefit(s) to thrombocytopenic patients by improving platelet numbers.

Timeline

Start
2010-06
Primary completion
2015-01
Completion
2015-03

Drugs

EvaluationDrugModalityDoseRoute
Comparator Eltrombopag Small molecule 100 mg Oral

Indications