BREAKING NEWS: New drug approved by the FDA for Duchenne muscular dystrophy. Learn more about this new treatment option.

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The CIFFREO Study

Activity Snapshot

Activity Type: 
On-Demand Webinar
Release Date: 
Tuesday, July 5, 2022
Sponsor Information: 

This Industry Update Webinar is sponsored by Pfizer. This program is not sponsored, endorsed, or accredited by MDA.

Faculty

Kasia Lobello, MD
Global Clinical Lead
Duchenne Muscular Dystrophy Gene Therapy Program Pfizer
Activity Overview: 

This Industry Update Webinar for clinicians is presented by Pfizer and features information on the CIFFREO study. On June 15, 2022 at 12:00PM EST in a 30-minutes webinar, Dr. Kasia Labello, Global Clinical Lead for the Duchenne Muscular Dystrophy Gene Therapy Program at Pfizer, provided an overview of the CIFFREO study. The CIFFREO Study is a Phase 3, Global, Multicenter, Randomized, Double-blind, Placebo-controlled Study to Assess the Safety and Efficacy of mini-dystrophin Gene Therapy (fordadistrogene movaparvovec) in Ambulatory Boys with DMD.