Give your opinion on a genetically modified drug for the treatment of Duchenne muscular dystrophy

Source: FAMHP

September 29, 2020

The FPS Public Health and FAMHP would like to invite you to take part in the public consultation on a clinical trial testing the genetically modified drug PF-06939926 for the treatment of Duchenne muscular dystrophy. The public consultation will run from 23 September 2020 to 23 October 2020.

For each clinical trial application related to the use of genetically modified organisms, the authority organises a public consultation lasting 30 days (in accordance with the Royal Decree of 21 February 2005). This gives you the opportunity, as a citizen, to share your opinion on the clinical trial application for the genetically modified drug PF-06939926 for the treatment of Duchenne muscular dystrophy. More information.