A 4-year Extension Study to Core 1-year Study of Iron Chelation Therapy With Deferasirox in β-thalassemia Major Pediatric Patients With Transfusional Iron Overload.

PHASE2CompletedINTERVENTIONAL
Enrollment

40

Participants

Timeline

Start Date

September 30, 2003

Primary Completion Date

February 29, 2008

Study Completion Date

February 29, 2008

Conditions
Transfusional Iron Overloadβ-thalassemia MajorPediatric Rare Anemia
Interventions
DRUG

Deferasirox

Deferasirox in children from 1 to 18 years old was given orally once daily, 30 minutes prior to breakfast. An initial daily dose of 10 mg/kg was used during the 1-year core study. In this 4-year extension study dose modifications of ± 5 or 10 mg/kg were based on safety parameters and on increasing or decreasing Liver Iron Concentration (LIC), and serum ferritin. Deferasirox was available as 125 mg, 250 mg and 500 mg tablets.

Trial Locations (4)

Unknown

Novartis Investigative Site, Lyon

Novartis Investigative Site, Cagliari

Novartis Investigative Site, Genova

Novartis Investigative Site, Torino

Sponsors
All Listed Sponsors
lead

Novartis Pharmaceuticals

INDUSTRY