Earlier this year, 109 members of the House of Representatives sent a powerful letter to the FDA urging them to “utilize all available tools, resources, and authorities” in reviewing a treatment for Duchenne muscular dystrophy. Congressional champions Congressmen Mike Fitzpatrick (R-PA), Bill Keating (D-MA), and Peter King (R-NY) led this incredible bipartisan letter. It was because of YOU and your advocacy that we were able to get 109 signatures!
We are now ready to turn to the Senate!
In an effort to make the message from Congress bicameral (both House and Senate) with one unified voice, our long-standing champions in the Senate, Senator Roger Wicker (R-MS) and Senator Amy Klobuchar (D-MN) are leading a similar Senate letter urging the FDA to utilize all available resources and authorities to accelerate the process of getting safe and effective treatments to Duchenne patients. Senator Elizabeth Warren (D-MA) has already signed on as an original co-signer!
With only a few weeks left before Sarepta’s Advisory Committee Meeting with the FDA and in anticipation of future Ad Comms and FDA product reviews, we need everyone to reach out to your two Senators today and urge them to sign this important letter, to help ensure that the FDA is using all available tools during the review process.
Please urge your Senators to join this effort by signing this important letter. Patients need and deserve therapeutic options and the FDA must use the tools they have been given to expedite these options.
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