Sarepta cites 'overburdened' FDA as factor in DMD gene therapy delay

Sarepta cites 'overburdened' FDA as factor in DMD gene therapy delay

Source: 
Fierce Biotech
snippet: 

Burdens placed on the FDA by COVID-19 and the rapid proliferation of cell and gene therapies are a factor in the recent setback to Sarepta Therapeutics’ Duchenne muscular dystrophy (DMD) prospect, according to CEO Douglas Ingram.