An Open Label Study to Evaluate the Pharmacokinetics, Safety, Tolerability and Efficacy of Deferasirox Administered to Chinese Patients With β-thalassemia Major Aged From 2 to Less Than 6 Years Old

PHASE4WithdrawnINTERVENTIONAL
0
Timeline

Start Date

June 30, 2013

Primary Completion Date

April 30, 2014

Study Completion Date

October 31, 2014

Conditions
β-thalassemia Major
Interventions
DRUG

Deferasirox

Patients will start their deferasirox treatment with a dose of 20 mg/kg/day.

Sponsors
All Listed Sponsors
lead

Novartis Pharmaceuticals

INDUSTRY