Justin’s Blog – The Chris Carrino Foundation for FSHD

Avidity Shares Promising Interim Data from its FORTITUDE Trial

by ccfshd_admin1Justin's Blog July 12, 2024No Comments

By Justin Cohen, PhD Avidity Biosciences recently announced exciting interim results from their randomized, double-blind, placebo-controlled Phase 1/2 FORTITUDE trial in facioscapulohumeral muscular dystrophy (FSHD). Termed delpacibart braxlosiran or del-brax for short, this first-in-class therapy is a muscle targeting antibody bound to a payload that targets DUX4, the toxic protein that causes FSHD. Once attached …

Hope for the Future of Muscular Dystrophy Treatment: Kate Therapeutics Harnesses their myoAAV Technology for FSHD

by ccfshd_admin1Justin's Blog July 8, 2023September 17, 2023No Comments

By Justin Cohen, PhD Kate Therapeutics, a San Diego base biotechnology company has announced funding to advance their muscle and cardiovascular disease portfolio. Among the first diseases to be explored is Facioscapulohumeral muscular dystrophy (FSHD), exciting news for patients like myself and their families who are impacted from this affliction. Included among these ranks is …

Breaking Barriers in the Sky: The Future of Air-Travel for Wheelchair Users

by ccfshd_admin1Justin's Blog June 30, 2023September 17, 2023No Comments

By Justin Cohen, PhD Air-travel for wheelchair users come with a unique set of challenges that cause many to forgo the plane altogether. This could all change after the recent Aircraft Interiors Expo in Hamburg, Germany, which unveiled a new airplane seat prototype that could revolutionize air-travel for wheelchair users. In a collaboration with the …

Justin Cohen: Living with FSHD, and efforting to find a cure

by ccfshd_admin1Justin's Blog November 30, 2019September 13, 2023No Comments

Justin Cohen is a remarkable young researcher, living with FSHD, and efforting to find a cure for the disease. The Carrino Foundation is proud to make his work possible. Here is Justin’s story, in his own words.