[Congressional Record Volume 162, Number 66 (Thursday, April 28, 2016)]
[Senate]
[Pages S2513-S2514]
From the Congressional Record Online through the Government Publishing Office [www.gpo.gov]
DUCHENNE MUSCULAR DYSTROPHY
Mr. WICKER. Mr. President, the fight against muscular dystrophy is a
cause I have championed since my days in the House of Representatives.
My fight against Duchenne muscular dystrophy began when a parent told
me about his son's diagnosis with the disease.
This parent refused to accept that there was no hope. The House and
Senate agreed with the MD-CARE Act and, since that time, the life
expectancy of the average Duchenne muscular dystrophy patient has
increased by a full decade. This is progress we have made on behalf of
sick people whose lives were threatened, and this is an example of
government at its best.
On Monday of this week, I saw the same devotion in the hundreds of
Duchenne families who attended a meeting of the advisers of the Food
and Drug Administration. The meeting's attendance broke records. I
thank the FDA for making the appropriate accommodations to handle a
crowd of this size. Some 11,000 people also tuned in remotely, watching
the meeting via live stream.
Monday's gathering was about what could be the first disease-
modifying therapy for Duchenne muscular dystrophy. For more than 3
hours, the advisory committee heard from parents, doctors, and patients
about the drug's impact on their lives. The stories were heartfelt and
hopeful, reinforcing the importance of patient engagement in the drug
approval process. The dedication of the Duchenne community continues to
set an example for advocates of other rare diseases.
Patient voices should be part of the drug review process, and I am
glad to see the FDA is implementing greater stakeholder involvement in
this process. This was one of the goals of the Food and Drug
Administration Safety and Innovation Act, which Congress passed in
2012. It continues to be a goal of my Patient-Focused Impact Assessment
Act, introduced last year, which would require FDA to share how they
use feedback from patients and advocates in the drug approval process.
Unfortunately, the advisory committee decided this week not to
recommend the approval of the first Duchenne drug. This is
disappointing news for me and for thousands of Duchenne families, even
those who might not benefit directly from this drug but from other
advancements that could stem from it.
Before a final decision is made next month, I hope the FDA will take
into consideration the perspectives of Duchenne patients and parents.
The individuals fighting the good fight every day are ``the real
experts,'' to quote Austin Leclaire, who suffers from Duchenne and has
experienced increased mobility because of the drug. People like Austin
have a life-threatening disease now. They don't have much time.
No matter the outcome of the FDA's decision next month, I will
continue to fight the good fight on behalf of those with Duchenne
muscular dystrophy. In the 15 years since I introduced the MD-CARE, I
have learned that small wins can lead to big victories.
MD-CARE was the first Federal law to focus on muscular dystrophy. It
helped set in motion the research and
[[Page S2514]]
trials that have produced groundbreaking therapies. The life of
muscular dystrophy patients now is an average of 12 years longer--I
think I earlier said a decade; it is actually 12 years longer than it
was in 2001--a wonderful achievement. There are more trial participants
needed today than there are Duchenne patients.
Young adults with Duchenne were a population that did not exist when
we first funded research for the disease. They never got to adulthood.
Today they are getting to adulthood because Congress acted. Because of
the MD-CARE amendments that became law last Congress, research at the
National Institutes of Health has been updated in ways that could help
patients lead even longer, healthier lives. We want this research to
continue. We want companies to continue to invest in drugs and
therapies that could change the lives of those with rare diseases.
Duchenne is still a fatal disease, affecting 1 out of every 3,500
boys--mostly boys. Most young men with Duchenne live only to their mid
to late twenties. We should take every opportunity to find a
breakthrough. We should take every opportunity to improve quality of
life. This is about the futures of young people who face this disease
every day and the families who refuse to give up hope.
I look forward to the FDA's full and final decision on this matter
next month, and I certainly am hoping for a positive answer from the
FDA.
Thank you.
I yield the floor.
The PRESIDING OFFICER. The Senator from South Dakota.
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