drugset / Trial / NCT00947193

Study of Ataluren (PTC124) in Hemophilia A and B

NCT00947193

Phase 2 Terminated 13 enrolled PTC Therapeutics Genzyme, a Sanofi Company · collab
NaSingle-groupOpen-labelTreatment

Summary

Hemophilia A (HA) and hemophilia B (HB) are inherited bleeding disorders caused by mutations in the gene for factor VIII (FVIII) and factor IX (FIX), respectively. These proteins are essential for blood clotting. The lack of FVIII/FIX can produce bleeding episodes that cause damage of the bone, muscles, joints, and tissues. A specific type of mutation, called a nonsense (premature stop codon) mutation, is the cause of the disease in approximately 10-30% of participants with hemophilia and results in severe manifestations. Ataluren (PTC124) is an orally delivered, investigational drug that acts to overcome the effects of the premature stop codon, potentially enabling the production of functional FVIII/FIX. This study is a Phase 2a trial evaluating the safety and efficacy of ataluren in participants with HA or HB due to a nonsense mutation. The main purpose of this study is to understand whether ataluren can safely increase FVIII/FIX activity levels.

Timeline

Start
2009-10-14
Primary completion
2011-08-30
Completion
2011-08-30

Drugs

EvaluationDrugModalityDoseRoute
Subject Ataluren Small molecule 5 mg/kg Oral
Subject Ataluren Small molecule 10 mg/kg Oral