drugset / Trial / NCT00110799

SB497115 (Oral Thrombopoietin Receptor Agonist) Versus Placebo In Adults With Thrombocytopenia Due To Hepatitis C

NCT00110799

Phase 2 Completed 75 enrolled GlaxoSmithKline
RandomizedParallel-groupQuadruple-blindTreatment

Summary

SB497115 is an oral agent which activates the thrombopoietin receptor and increases platelet counts in healthy volunteers. This study is examining several different doses of SB497115 as a treatment for patients with chronic hepatitis C-related thrombocytopenia who are potential candidates for antiviral treatment with pegylated interferon and ribavirin. The study will be conducted in two phases, Parts 1 and 2. In Part 1, study subjects will be randomized to 4 weeks of SB-497115-GR or placebo administered daily without antiviral therapy. Subjects who successfully complete Part 1 (platelet count 70,000/µL for Pegasys and platelet count 100,000/µL for PEG-Intron) will then proceed to Part 2. In Part 2, subjects will receive an additional 8 weeks of SB-497115-GR or placebo administered daily with antiviral therapy.

Timeline

Start
2005-04
Primary completion
2006-10
Completion
2006-11

Drugs

EvaluationDrugModalityDoseRoute
Comparator Eltrombopag Small molecule 30 mg Oral
Comparator Eltrombopag Small molecule 50 mg Oral
Comparator Eltrombopag Small molecule 75 mg Oral