drugset / Trial / NCT01825512
Efficacy/Safety Study of Deferiprone Compared to Deferasirox in Paediatric Patients
Phase 3
Completed
435 enrolled
Consorzio per Valutazioni Biologiche e Farmacologiche
European Commission · collab
RandomizedParallel-groupOpen-labelTreatment
Summary
Multicentre, randomised, open label, non-inferiority active-controlled trial to evaluate efficacy and safety of a 12-months treatment with deferiprone (DFP) at dose of 75-100 mg/kg/day versus deferasirox (DFX) at dose of 20-40 mg/kg/day in paediatric patients (1 month \< 18 years old) affected by hereditary haemoglobinopathies and requiring frequent transfusions and chelation.
Timeline
- Start
- 2014-03-17
- Primary completion
- 2017-09-21
- Completion
- 2017-09-21
Publications
- Giannuzzi V, Felisi M, Bonifazi D, Devlieger H, Papanikolaou G, Ragab L, Fattoum S, Tempesta B, Reggiardo G, Ceci A. Ethical and procedural issues for applying researcher-driven multi-national paediatric clinical trials in and outside the European Union: the challenging experience of the DEEP project. BMC Med Ethics. 2021 Apr 29;22(1):49. doi: 10.1186/s12910-021-00618-2.
- Maggio A, Kattamis A, Felisi M, Reggiardo G, El-Beshlawy A, Bejaoui M, Sherief L, Christou S, Cosmi C, Della Pasqua O, Del Vecchio GC, Filosa A, Cuccia L, Hassab H, Kreka M, Origa R, Putti MC, Spino M, Telfer P, Tempesta B, Vitrano A, Tsang YC, Zaka A, Tricta F, Bonifazi D, Ceci A. Evaluation of the efficacy and safety of deferiprone compared with deferasirox in paediatric patients with transfusion-dependent haemoglobinopathies (DEEP-2): a multicentre, randomised, open-label, non-inferiority, phase 3 trial. Lancet Haematol. 2020 Jun;7(6):e469-e478. doi: 10.1016/S2352-3026(20)30100-9.
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Comparator | Deferasirox | Unknown | 20 mg/kg | Oral |
| Comparator | Deferasirox | Unknown | 40 mg/kg | Oral |
| Subject | Deferiprone | Small molecule | 75 mg/kg | Oral |
| Subject | Deferiprone | Small molecule | 100 mg/kg | Oral |