We are thrilled to report that last night the Ensuring Access to Clinical Trials Act of 2015 (EACT) passed a vote in the House of Representatives (after passing the Senate by unanimous consent in July) and will go to the President for his signature!
This a result of everyone who contacted their Representative – over 400 families in…
ContinueAdded by Ryan Fischer on September 29, 2015 at 11:08am — No Comments
URGE THE SENATE TO PRIORITIZE CURES!
One minute of your day could mean millions of minutes for those diagnosed with Duchenne.
Today, patient advocates from across the country will unite in a day of action to urge the Senate to make medical innovation a top priority.
Earlier this year the Duchenne…
ContinueAdded by Ryan Fischer on September 25, 2015 at 9:30am — No Comments
As we make advancements in Duchenne drug development, the potential therapeutic opportunities for Duchenne patients across the spectrum of the disease continues to grow — as do the opportunities to participate in clinical trials. This is a hopeful and exciting time for our Duchenne community and we must ensure unnecessary barriers don’t hamper clinical…
ContinueAdded by Ryan Fischer on September 18, 2015 at 10:29am — No Comments
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