Safety and Acceptability of Deferiprone Delayed Release Tablets in Patients With Systemic Iron Overload

PHASE2CompletedINTERVENTIONAL
Enrollment

30

Participants

Timeline

Start Date

March 6, 2019

Primary Completion Date

December 4, 2019

Study Completion Date

December 19, 2019

Conditions
Iron Overload Due to Repeated Red Blood Cell Transfusions
Interventions
DRUG

Deferiprone DR tablets 1000 mg (Low dosage)

Deferiprone DR tablets 1000 mg

DRUG

Deferiprone DR tablets 1000 mg (High dosage)

Deferiprone DR tablets 1000 mg

Trial Locations (5)

10043

San Luigi Gonzaga University Hospital Reparto Microcitemie-Pediatria, Orbassano (TO)

10065

New York Presbyterian Hospital/Weill Cornell Medical Center, New York

11527

National and Kapodistrian University of Athens, Aghia Sophia Children's Hospital, Goudi

60611

Ann & Robert H. Lurie Children's Hospital of Chicago, Chicago

V6Z 1Y6

St.Paul's Hospital, Vancouver

Sponsors

Lead Sponsor

All Listed Sponsors
lead

ApoPharma

INDUSTRY

NCT03802916 - Safety and Acceptability of Deferiprone Delayed Release Tablets in Patients With Systemic Iron Overload | Biotech Hunter | Biotech Hunter