CureDuchenne Founder and CEO Debra Miller is an EY Entrepreneur of the Year 2014 Award Finalist in Orange County

CureDuchenne is pleased to announce that Debra Miller, founder and CEO of CureDuchenne, is a finalist for the EY Entrepreneur Of The YearÌ¢‰Û_å¢ 2014 Award in Orange County. The awards program recognizes entrepreneurs who demonstrate excellence and extraordinary success in such areas as innovation, financial performance and personal commitment to their businesses and communities. Miller was selected as a finalist from nearly 80 applications by a panel of independent judges. Award winners will be announced at a special gala event on June 4, 2014 at The St. Regis Resort in Dana Point.

Sarepta to Host Webinar Tuesday, May 13

  Sarepta Therapeutics, Inc. will host a webcast and conference call for the Duchenne muscular dystrophy (DMD) community on Tuesday, May 13, 2014, beginning at 11:00 am EDT (8:00 am […]

Prosensa Provides Update on Drisapersen

Re-dosing plans are underway and 96-week data from an open-label extension study of drisapersen for the treatment of DMD presented at the American Academy of Neurology (AAN) Leiden, The Netherlands, […]

Sarepta to File Eteplirsen NDA by Year End

Summary from Seeking Alpha Based on updated guidance from the FDA regarding an  early approval pathway for eteplirsen, Sarepta Therapeutics (SRPT) plans to file an NDA by the end of 2014. The […]

Champions to CureDuchenne Newport Beach Gala Raises More Than $360,000 to Fund Duchenne Muscular Dystrophy Research

CureDuchenne, a nonprofit that raises awareness and funds research to find a cure for Duchenne muscular dystrophy, held its annual Champions to CureDuchenne Newport Beach Gala on March 29 at the Balboa Bay Club & Resort. More than 250 guests attended the gala that celebrated CureDuchenneÌ¢‰â‰ã¢s 10 years of successfully advancing Duchenne research. The event raised more than $360,000 that will fund promising Duchenne research.

Drisapersen Update with Prosensa

Prosensa will present a status update on Drisapersen and its follow-on compounds in a patient focused webinar hosted by United Parent Projects Muscular Dystrophy (UPPMD) on Tuesday, March 25 at […]