Effect of Deferiprone on Oxidative-Stress and Iron-Overload in Low Risk Transfusion-Dependent MDS Patients

PHASE2CompletedINTERVENTIONAL
Enrollment

19

Participants

Timeline

Start Date

February 29, 2016

Primary Completion Date

May 31, 2017

Study Completion Date

June 30, 2018

Conditions
Myelodysplastic Syndrome With Low-grade LesionsIron Overload Due to Repeated Red Blood Cell Transfusions
Interventions
DRUG

Deferiprone

This is a single-arm, open-label, multi-center study in 20 patients with MDS. All participants will be treated with deferiprone for up to 4 months.

Trial Locations (1)

52621

Chim Sheba Medical Center, Tel Litwinsky

Sponsors

Collaborators (1)

All Listed Sponsors
collaborator

Hadassah Medical Organization

OTHER

collaborator

Tel Aviv Medical Center

OTHER

collaborator

Kaplan Medical Center

OTHER

collaborator

Ziv Medical Center

OTHER

lead

Sheba Medical Center

OTHER_GOV

NCT02477631 - Effect of Deferiprone on Oxidative-Stress and Iron-Overload in Low Risk Transfusion-Dependent MDS Patients | Biotech Hunter | Biotech Hunter