FDA Sets May 1 PDUFA Action Date for uniQure’s Huntington’s Disease Gene Therapy
uniQure has aligned with the FDA on what the company calls key elements of the confirmatory study design: The study is being designed as a randomized, standard-of-care trial enrolling approximately 200 patients in a 2:1 ratio of ifezuntirgene inilparvovec to standard of care, with Total Functional…
Sources
- T2FDA Sets May 1 PDUFA Action Date for uniQure’s Huntington’s Disease Gene TherapyFierce Biotech / Fierce Healthcare / MedCity / GEN