[Congressional Record Volume 163, Number 132 (Thursday, August 3, 2017)]
[Senate]
[Pages S4809-S4810]
From the Congressional Record Online through the Government Publishing Office [www.gpo.gov]
BENEFIT ACT
Mr. WICKER. Mr. President, my esteemed colleague from Delaware says
that we have plenty to do when we get back, and he is, certainly,
correct. I would join many of my colleagues today, though, in pointing
out that in the last 3 days, we have actually gotten substantial work
done. Perhaps we have crammed into 3 days what using the regular order
and the filibuster and the motions to proceed might have taken 3 weeks
otherwise. So the leadership on both sides of the aisle are to be
commended for this burst of progress we have made, and I hope we can
continue that when we get back.
Earlier today, this Congress passed a significant piece of
legislation offered by the Senator who occupies the Chair, my good
friend, Senator Johnson of Wisconsin. It is the Right to Try Act, which
seeks to streamline the way people who are willing to take a bit of a
chance on a drug in order to save their lives--streamline the way they
can have access to perhaps life-enhancing and lifesaving drugs. It is a
real achievement. I congratulate my colleague from Wisconsin and
congratulate the leadership facilitating this breakthrough.
Moments later, the Senate passed a companion bill authored by Senator
Klobuchar and me known as the Better Empowerment Now to Enhance
Framework and Improve Treatments Act or the BENEFIT Act. This is
another win for patients--patients who deserve to have a voice in the
drug approval process. This bill, which is a companion bill to the very
important Right to Try Act, will do that.
The BENEFIT Act calls for a simple amendment to the Food, Drug, and
Cosmetic Act--one that could make a big difference to patients whose
lives may depend on a new therapy or drug. Specifically, the Wicker-
Klobuchar bill would require the use of patient experience and patient-
focused drug development and related data in assessing the risk versus
the benefit of these particular therapies.
The bill also includes information from patient advocacy groups and
academic institutions. This is a small but important step forward.
If signed into law--and I certainly hope the House passes it and I
hope the President will sign it into law--this bill would greatly
enhance the data and information available to FDA when reviewing drugs,
when reviewing medical products, and when reviewing therapies. It would
also add to the progress Congress has made in recent years, reaffirming
the importance of patients' perspectives in drug decisions--decisions
that can have a profound and lasting impact on the lives of these
patients. Ask any American who suffers from a disease or who is
watching a loved one suffer, and they will tell us that all information
should be on the table when a breakthrough or a cure is at stake.
Last year, Senator Klobuchar and I joined together to make the FDA's
use of patient perspectives more transparent with what we call the
Patient-Focused Impact Assessment Act. This was passed and was signed
into law as part of the 21st Century Cures Act.
The BENEFIT Act, passed by the Senate today, would keep that momentum
going, building on the progress we have made.
Now, what progress have we made? Let me tell my colleagues this. For
years, I have sought to find a cure for the devastating, fatal disease
known as Duchenne muscular dystrophy. I have worked on this issue since
my early years in the House of Representatives. Young boys--almost all
males--is whom this affects. These young boys face this fatal disease,
and they know better than anyone what a drug can do to improve the
quality of their lives.
Since the Congress passed and the President signed the MD-CARE Act
dealing with Duchenne muscular dystrophy more than 15 years ago,
research has led to innovative therapies
[[Page S4810]]
that have added a decade to the lives of these young boys. What an
achievement by scientists in America. What an achievement for the
government to have unleashed cures and research in this area.
We need their voices heard, we need their stories heard, and we need
the voices of patients with other diseases heard.
I thank my colleagues in the Senate for joining with us on a
unanimous consent request to pass this legislation. I thank the
leadership on this side of the aisle and our Democratic counterparts on
the other side.
Particular appreciation goes to Senator Alexander, the chairman of
the HELP Committee, and to Senator Murray, the ranking Democrat on the
HELP Committee, for their valuable help. Appreciation goes to perhaps a
new attitude for the rest of the year in the Senate to join together
with unanimous consent and move bills and nominations forward that have
widespread support and consensus around the country.
I congratulate the Presiding Officer, the Senator from Wisconsin, on
an outstanding achievement, and I congratulate the Senate for joining
with Senator Klobuchar and me to help out in another way.
Thank you.
I yield the floor.
I suggest the absence of a quorum.
The PRESIDING OFFICER. The clerk will call the roll.
The senior assistant legislative clerk proceeded to call the roll.
Mr. WICKER. Mr. President, I ask unanimous consent that the order for
the quorum call be rescinded.
The PRESIDING OFFICER. Without objection, it is so ordered.
____________________