ALS Placebo No More Act
This bill requires the Food and Drug Administration and the National Institutes of Health to collaborate to provide all patients with ALS (amyotrophic lateral sclerosis, also referred to as Lou Gehrig's disease) with access to medicines in clinical trials.
[Congressional Bills 116th Congress]
[From the U.S. Government Publishing Office]
[H.R. 5480 Introduced in House (IH)]
<DOC>
116th CONGRESS
1st Session
H. R. 5480
To ensure that ALS patients have access to treatment within clinical
trials.
_______________________________________________________________________
IN THE HOUSE OF REPRESENTATIVES
December 18, 2019
Mr. Fortenberry introduced the following bill; which was referred to
the Committee on Energy and Commerce
_______________________________________________________________________
A BILL
To ensure that ALS patients have access to treatment within clinical
trials.
Be it enacted by the Senate and House of Representatives of the
United States of America in Congress assembled,
SECTION 1. SHORT TITLE.
This Act may be cited as the ``ALS Placebo No More Act''.
SEC. 2. AUTHORITY FOR HHS AND AGENCIES TO DEVELOP RESOURCES AND
POLICIES TO PROVIDE ACCESS TO PROMISING TREATMENTS FOR
PATIENTS WITH ALS.
The Food and Drug Administration (FDA) and the National Institutes
of Health (NIH) shall collaborate on any current amyotrophic lateral
sclerosis (ALS) trial to ensure that all patients in treatment and
placebo arms are provided access to the drug.
The FDA shall move expeditiously to implement its guidance on ALS
clinical trials to assure that all trials going forward shall require
treatment arms for all patients.
The Federal Government shall develop incentives to expand access to
investigational therapies for life-threatening conditions with fewer
than two treatments.
<all>
Introduced in House
Introduced in House
Referred to the House Committee on Energy and Commerce.
Referred to the Subcommittee on Health.
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