Guideline on the clinical investigation of medicinal products for the treatment of Duchenne and Becker muscular dystrophy

We have adopted this International Scientific Guideline - EMA/CHMP/236981/2011, Corr. 1.

Last updated

3 June 2024

About this guideline

Adopted by the TGA: 28 February 2020

Overseas effective date: 1 July 2016

Categories: Clinical efficacy and safety | Nervous system

TGA annotations: Nil

Where EU guidelines adopted in Australia include references to EU legislation (including EC Directives and Regulations), the requirements contained in the referenced EU legislation are not applicable to the evaluation of medicines by the TGA.
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