Cart
×
September 21, 2023
CureDuchenne to offer free new virtual resource for DMD caregivers (Muscular Dystrophy News)September 21, 2023
CureDuchenne launches the CureDuchenne Caregiver Course: a free virtual resource for Duchenne muscular dystrophy caregivers (Rare Revolution Magazine)September 18, 2023
Michael Kelly, PhD, on Continuing Progress With Gene Therapy in Muscular Dystrophy (CGT Live)September 13, 2023
Join the Ladies Luncheon Fundraiser in Austin benefitting nonprofit CureDuchenne, whose mission is to cure Duchenne Muscular Dystrophy (CBS8 Austin)August 31, 2023
The Cali-Rad Fest is Reggae For A Cause (FOX5 San Diego)August 30, 2023
Cali-Rad Fest benefits CureDuchenne (CBS8 San Diego)August 30, 2023
Dyne Therapeutics and CureDuchenne partner to give the gift of mobility to two local families (Rare Revolution Magazine)August 25, 2023
Top Philanthropists Announced for 38th Annual National Philanthropy Day Orange County (Newport Beach Independent)August 22, 2023
Tevard Biosciences Pursues Gene Therapy to Treat Dravet Syndrome and Possibly DMD (Rare Disease Advisor)August 21, 2023
Texas Family Raises Millions for Groundbreaking Duchenne Research (Rare Disease Advisor)August 16, 2023
NHL All-Star Ryan Getzlaf returns to the links for the 12th annual Getzlaf Golf Shootout on September 9 benefiting CureDuchenne (Rare Revolution Magazine)August 8, 2023
Annual Getzlaf Golf Shootout on Sept. 9 Will Benefit Newport Beach-based CureDuchenne (Newport Beach Independent)July 31, 2023
Edgewise and Locanabio Target New Mechanisms for Treating DMD (Rare Disease Advisor)July 24, 2023
FDA Greenlights 35 Novel Approvals in H1, Biologics Stand Out (BioSpace)July 14, 2023
Novel Trial May Make Patients With DMD Suitable for Gene Therapy (Rare Disease Advisor)July 12, 2023
Listen: One Duchenne patient’s bittersweet hope for new treatment (STAT First Opinion Podcast)June 30, 2023
For Duchenne moms who pushed for cures, new breakthrough therapy can’t rebuild what’s lost (STAT)June 23, 2023
The FDA’s approval of a new gene therapy for Duchenne muscular dystrophy won’t help me — but it gives me hope (STAT)June 23, 2023
An important milestone for the Duchenne community (Rare Revolution Magazine)June 23, 2023
Rare Community Profiles: A Partnership Between CureDuchenne and PicnicHealth Bolsters the Power of CureDuchenne Link (Patient Worthy)June 23, 2023
First gene therapy for certain DMD patients gains FDA nod (The Pharma Letter)June 23, 2023
Anecdotal evidence and urgent need sway FDA panel toward Sarepta’s DMD therapy (BioCentury)