Overview

Safety and Efficacy Study for Solid Tumor Patients Treated With Eltrombopag

Status:
Completed
Trial end date:
2015-03-01
Target enrollment:
Participant gender:
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.
Phase:
Phase 2
Details
Lead Sponsor:
GlaxoSmithKline