drugset / Trial / NCT00358540

Dose Finding Study Of Oral Eltrombopag In Patients With Sarcoma Receiving Adriamycin And Ifosfamide

NCT00358540

Phase 1 Completed 18 enrolled GlaxoSmithKline
Non-randomizedSingle-groupOpen-labelSupportive care

Summary

The study will evaluate the safety and tolerability, optimal biologic dose, and pharmacokinetics of eltrombopag for patients with advanced sarcoma who have a low platelet count and are receiving ADRIAMYCIN and ifosfamide (AI) chemotherapy.

Timeline

Start
2006-06-01
Primary completion
2010-10-22
Completion
2010-10-22

Drugs

EvaluationDrugModalityDoseRoute
Subject Eltrombopag Small molecule 75 mg Oral
Subject Eltrombopag Small molecule 100 mg Oral
Subject Eltrombopag Small molecule 150 mg Oral

Indications