A Phase II, Open Label, Extension Study to Assess the Effect of PRO044 in Patients With Duchenne Muscular Dystrophy

Status: Discontinued

Phase of Trial: Phase II

Latest Information Update: 06 Nov 2021

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At a glance

31 May 2016 According to a BioMarin media release, the company intends to discontinue clinical and regulatory development of Kyndrisa as well as the three other first-generation follow-on products, BMN 044, BMN 045 and BMN 053, currently in Phase 2 studies for distinct forms of Duchenne muscular dystrophy.
31 May 2016 Status changed from recruiting to discontinued, according to a BioMarin media release.
31 Mar 2015 New source identified and integrated (European Clinical Trials Database record; EudraCT2013-003605-26).

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