A suggestion to the desperate DMD parents, Contact your state's attorney general's office and report that the FDA is "killing" your son[s] due to special interest influence. I believe if the AG's office subpoenaed the MD's on the FDA panel that made irresponsible comments at the Sarepta meeting by citing a different inferior drug, at a sub therapeutic dose, as reason for reversing their very favorable comments supporting AA for eteplirsen, they will find "gift" payments to many of these MD's in their financials from GSK. This might sound extreme to many here but these families are desperate and I would do anything to save my son. This is gov't corruption at it's worse. Is the FDA aware that the 2012 FDASIA law directs them to use "surrogate" and "intermediate" endpoints to approve drugs for life-saving therapies???
Sentiment: Strong Buy