[Congressional Bills 119th Congress]
[From the U.S. Government Publishing Office]
[H.R. 10212 Introduced in House (IH)]

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119th CONGRESS
  2d Session
                               H. R. 10212

  To direct the Secretary of Veterans Affairs to study the potential 
benefits of peptide-based therapies for veterans receiving care through 
      the Department of Veterans Affairs, and for other purposes.


_______________________________________________________________________


                    IN THE HOUSE OF REPRESENTATIVES

                           September 1, 2026

   Ms. Mace introduced the following bill; which was referred to the 
                     Committee on Veterans' Affairs

_______________________________________________________________________

                                 A BILL


 
  To direct the Secretary of Veterans Affairs to study the potential 
benefits of peptide-based therapies for veterans receiving care through 
      the Department of Veterans Affairs, and for other purposes.

    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 ``Providing Evidence-based Peptide 
Therapies to Improve Delivery and Expanded Services for Veterans Act'' 
or the ``PEPTIDES for Veterans Act''.

SEC. 2. REVIEW OF REGULATIONS AND GUIDANCE RELATING TO PEPTIDES.

    (a) Review Required.--The Secretary of Veterans Affairs shall 
conduct a review of the regulations and guidance relating to peptides 
and, in particular, the scope of ``peptide'' as a defined term in 
Federal regulations and guidance, and shall establish an appropriate 
definition of ``peptide'' for purposes of this Act. A primary focus of 
the review shall be to consider addressing developments in research 
relating to peptides, if any, since the regulations, guidance, and 
defined terms were established.
    (b) Report.--Not later than 180 days after the date of the 
enactment of this Act, the Secretary shall submit to Congress a report 
on the results of the review. The report shall--
            (1) summarize the regulations, guidance, and defined terms;
            (2) describe the research developments, if any, since the 
        regulations, guidance, and defined terms were established;
            (3) set forth the definition of ``peptide'' established by 
        the Secretary for purposes of this Act;
            (4) set forth a definition of ``peptide-based therapy'' for 
        purposes of this Act and any guidance the Secretary determines 
        to be appropriate regarding what constitutes such a therapy; 
        and
            (5) explain the rationale for the definition established by 
        the Secretary and the differences, if any, between such 
        definition and other definitions of ``peptide'' in Federal 
        regulations and guidance.

SEC. 3. STUDY ON POTENTIAL BENEFITS OF PEPTIDE-BASED THERAPIES FOR 
              VETERANS AND PILOT PROGRAM TO EVALUATE THERAPIES.

    (a) Study Required.--
            (1) In general.--Beginning on the date on which the report 
        required by section 2 is submitted to Congress, the Secretary 
        of Veterans Affairs shall carry out a study on the safety, 
        efficacy, and potential therapeutic benefits of peptide-based 
        therapies for veterans receiving care at medical facilities of 
        the Department of Veterans Affairs.
            (2) Matters included.--In carrying out the study, the 
        Secretary shall--
                    (A) review medical research;
                    (B) establish clinical protocols;
                    (C) identify potential applications relating to 
                recovery, rehabilitation, chronic pain, mental health, 
                physical wellness, and other service-connected 
                conditions affecting veterans; and
                    (D) consider the extent to which peptides are safe 
                to use for clinical and rehabilitation purposes.
            (3) Completion of study.--The study shall be completed not 
        later than the date that is 18 months after the date on which 
        the report required by section 2 is submitted to Congress.
            (4) Report.--Upon completing the study, the Secretary shall 
        submit to Congress a report on the results of the study. The 
        report shall include findings, recommendations, and a 
        determination as to whether peptide-based therapies should be 
        made available to veterans receiving care at medical facilities 
        of the Department of Veterans Affairs.
    (b) Pilot Program.--
            (1) In general.--If the Secretary determines, in the report 
        required by subsection (a)(4), that peptide-based therapies 
        should be provided to such veterans, then the Secretary shall 
        carry out a pilot program under which peptide-based therapies 
        are made available to such veterans and the results of those 
        therapies are assessed.
            (2) Limitations on pilot program.--Participation in the 
        pilot program shall be limited to veterans who elect to 
        participate, and the Secretary shall impose such other 
        geographic, clinical, or other limitations on the pilot program 
        as the Secretary considers appropriate.
            (3) Completion of pilot program.--The pilot program shall 
        be completed not later than the date that is 5 years after the 
        date on which it is established.
            (4) Report.--Upon completing the pilot program, the 
        Secretary shall submit to Congress a report on the results of 
        the pilot program. The report shall include--
                    (A) a detailed description of the effectiveness of 
                peptide treatments for clinical and rehabilitation 
                purposes, including a determination as to what 
                conditions or ailments are improved by use of peptides;
                    (B) guidance on large-scale implementation of 
                peptides throughout the medical facilities of the 
                Department; and
                    (C) any challenges encountered in carrying out the 
                pilot program.
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