[Congressional Bills 118th Congress]
[From the U.S. Government Publishing Office]
[S. 607 Introduced in Senate (IS)]

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118th CONGRESS
  1st Session
                                 S. 607

To allow the Secretary of Health and Human Services to deny approval of 
  a new drug application for an opioid analgesic drug on the basis of 
such drug not being clinically superior to other commercially available 
                                 drugs.


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                   IN THE SENATE OF THE UNITED STATES

                             March 1, 2023

Mr. Manchin (for himself and Mr. Braun) introduced the following bill; 
     which was read twice and referred to the Committee on Health, 
                     Education, Labor, and Pensions

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                                 A BILL


 
To allow the Secretary of Health and Human Services to deny approval of 
  a new drug application for an opioid analgesic drug on the basis of 
such drug not being clinically superior to other commercially available 
                                 drugs.

    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 ``Ensuring the FDA Fully Examines 
Clinical Trial Impact and Vitalness before Endorsement Act'' or the 
``EFFECTIVE Act''.

SEC. 2. REQUIREMENT FOR APPROVAL OF NEW OPIOID ANALGESICS.

    Section 505(c) of the Federal Food, Drug, and Cosmetic Act (21 
U.S.C. 355(c)) is amended by adding at the end the following:
    ``(6) Notwithstanding any other provision of this section, the 
Secretary may deny approval of an application submitted under 
subsection (b) for an opioid analgesic drug if the Secretary determines 
that such drug does not provide a significant advantage, in terms of 
greater safety or effectiveness, compared to an appropriate comparator 
drug, as determined by the Secretary.''.
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