作者
Eugenio Mercuri,Juan J. Vílchez,Odile Boespflüg-Tanguy,Craig M. Zaidman,Jean K. Mah,Nathalie Goemans,Wolfgang Müller‐Felber,E. Niks,Ulrike Schara‐Schmidt,Enrico Bertini,Giacomo P. Comi,Katherine D. Mathews,Laurent Servais,Krista Vandenborne,Jessika Johannsen,Sonia Messina,Stefan Spinty,Laura McAdam,Kathryn Selby,Barry J. Byrne,Chamindra G. Laverty,Kevin Carroll,Giulia Zardi,Sara Cazzaniga,N. Coceani,Paolo Bettica,Craig M. McDonald,Gyula Acsádi,Giovanni Baranello,Astrid Blaschek,John F. Brandsema,Claudia Brogna,Claudio Bruno,Anne M. Connolly,Imelda J. M. de Groot,Liesbeth De Waele,Erika Finanger,Richard S. Finkel,Teresa Gidaro,M. Guglieri,Amy Harper,Mercedes López Lobato,Marcos Madruga Garrido,Francesca Magri,Georgios Manousakis,Riccardo Masson,Migvis Monduy,Nuria Muelas Gomez,Francina Munell,A. Nascimento,Yoram Nevo,Yann Péréon,Han Phan,Valeria Sansone,Mariacristina Scoto,Dragana Vučinić,Tracey Willis
摘要
Duchenne muscular dystrophy, the most common childhood muscular dystrophy, is caused by dystrophin deficiency. Preclinical and phase 2 study data have suggested that givinostat, a histone deacetylase inhibitor, might help to counteract the effects of this deficiency. We aimed to evaluate the safety and efficacy of givinostat in the treatment of Duchenne muscular dystrophy.