This is historical material “frozen in time”. The website is no longer updated and links to external websites and some internal pages may not work.

Encourage the FDA to fast track approval of the drug Eteplirsen by Sarepta for Duchenne Muscular Dystrophy.

Created by A.J. on May 14, 2013

The pharmaceutical company Sarepta Therapeutics Inc.has created a medication named eteplirsen (also known as AVI-4658). It is designed for treatment of some mutations which cause Duchenne muscular dystrophy (DMD), a genetic degenerative muscle disease. This treatment could allow for victims of DMD to be active for longer periods, and prevent deterioration for longer.

There is currently no cure for DMD, and treatment methods to minimize symptoms would be greatly helped by this medication.

Please encourage the FDA to utilize the Fast Track process to consider approving Eteplirsen.

Health Care
Return to top