A Study to Assess Safety/Tolerability, pk, Effects on Histology, Clinical Parameters of Givinostat in Children With DMD

PHASE1/PHASE2CompletedINTERVENTIONAL
Enrollment

20

Participants

Timeline

Start Date

April 30, 2013

Primary Completion Date

December 31, 2014

Study Completion Date

November 30, 2017

Conditions
Duchenne Muscular Dystrophy (DMD)
Interventions
DRUG

Givinostat

Givinostat, oral suspension 10 mg/mL or oral capsules 50 mg, administered orally under fed conditions at the dose of 25 mg BID, 37.5 mg BID, and 50 mg BID during Part 1 for two weeks, and 25 mg BID and 37.5 mg BID during Part 2 for 12 months. Givinostat, oral suspension 10 mg/mL, administered orally under fed conditions at the dose of 25 mg BID or 37.5 mg BID during Extension 1, and modified as per patient's weight during Extensions 2 and 3 (up to 52 months).

Trial Locations (4)

20122

IRCCS Ca' Granda Ospedale Maggiore Policlinico di Milano, Milan

98125

Azienda Ospedaliera Universitaria Policlinico G. Martino, Messina

00168

Policlinico Agostino Gemelli, Roma

00165

Ospedale Pediatrico Bambino Gesù, Rome

Sponsors

Lead Sponsor

All Listed Sponsors
lead

Italfarmaco

INDUSTRY