SB 631: "Veterans Mental Health Innovations Act"; enact
Introduced version, the latest LegiScan holds · Last action March 25, 2026 · Introduced
The text as LegiScan holds it, read from the PDF the legislature publishes with its margin line numbers, running heads, and page footers removed. Line breaks are joined into paragraphs here; no word is changed.
Underlined words are what the bill adds to current law and struck-through words are what it removes, as the printed bill shows them.
Senate Bill 631
By: Senators Halpern of the 39th, Anderson of the 43rd, Wicks of the 34th, Jackson of the 41st and Parent of the 44th
A BILL TO BE ENTITLED
AN ACT
To amend Article 1 of Chapter 2A Title 31 of the Official Code of Georgia Annotated, relating to general provisions of the Department of Public Health, so as to authorize the department to award grants to eligible entities to conduct clinical trials approved by the United States Food and Drug Administration as a part of a multistate consortium using ibogaine as an investigational new drug for the treatment of opioid use disorder, co-occurring substance use disorder, and any other neurological or mental health conditions as related to veterans for which ibogaine demonstrates efficacy; to provide for waiver; to provide for definitions; to provide for revenue attributable to intellectual property rights and other commercial rights relative to clinical trials; to provide for the awarding of grants by the Department of Public Health; to provide for certain eligibility requirements; to provide for certain verifications; to provide for certain limitations on disbursement; to provide for reporting; to provide for construction; to provide for related matters; to provide for a short title; to provide for an effective date; to provide for contingencies; to repeal conflicting laws; and for other purposes.
BE IT ENACTED BY THE GENERAL ASSEMBLY OF GEORGIA:
SECTION 1.
This Act shall be known and may be cited as the "Veterans Mental Health Innovations Act."
SECTION 2.
Article 1 of Chapter 2A Title 31 of the Official Code of Georgia Annotated, relating to general provisions of the Department of Public Health, is amended by adding a new Code section to read as follows:
"31-2A-21.
(a) As used in this Code section, the term:
(1) 'Armed forces' means the United States army, navy, marine corps, space force, coast guard, air force, Georgia National Guard, or other reserve unit of the United States military.
(2) 'Clinical trial' means a clinical trial program approved by the federal Food and Drug Administration and conducted in this state as part of a multistate consortium for the investigational use of ibogaine for the treatment of opioid use disorder, co-occurring substance use disorder, and any other neurological or mental health conditions as related to veterans for which ibogaine demonstrates efficacy.
(3) 'Ibogaine' means ibogaine and ibogaine based therapeutics, including ibogaine analogs.
(4) 'Multistate consortium' means a collection of state, research institutions or state agencies from different states collaborating or associating for the purpose of conducting clinical trials concerning the medicinal use of ibogaine.
(5) 'Veteran' means a former member of the armed forces who received an honorable discharge.
(b) Subject to appropriations by the General Assembly for such purpose, the department shall be authorized to award grants to entities to participate in clinical trials, provided that the department has obtained a waiver or authorization from the federal government if such department determines that such waiver or authorization is required under federal law for the implementation of any provision of this Code section. The department shall only award a grant pursuant to this Code section to an applicant that:
(1) Is located within this state;
(2) Has a history of proven research and treatment of neurological conditions and expertise in substance dependence and emotional, physical or neurological trauma as related to veterans;
(3) Has a neurosurgery program with clinical and research facilities authorized to enter into a multistate consortium agreement and is:
(A) Staffed by professionals with expertise in neurological and neurosurgical conditions; and
(B) Capable of providing the necessary infrastructure and expertise to deliver cardiac intensive care services;
(4) Has the ability to facilitate research and innovation in the diagnosis and treatment of neurological conditions as related to veterans;
(5) Has demonstrated to the department that the entity has the financial capability to match moneys from gifts, grants, and donations from sources other than this state in the amount of at least $7 million to conduct the clinical trials described in this Code section; and
(6) Has agreed to enter into an agreement with a multistate consortium by which the applicant or an agent or joint venture thereof has agreed to:
(A) Submit an investigational new drug application to the United States Food and Drug Administration in accordance with 21 C.F.R. Part 312; and
(B) Request a breakthrough therapy designation for ibogaine from the United States Food and Drug Administration under 21 U.S.C. Section 356.
(c) An applicant selected to conduct clinical trials shall quarterly, prepare and submit to the department:
(1) A report on the progress of the clinical trials conducted under this Code section; and
(2) A financial status report, including information verifying expenditures of state funds and required matching funds.
(d) All revenue attributable to all intellectual property rights and other commercial rights that may arise from the clinical trials conducted by the entity receiving the grant described in subsection (b) of this Code section during the period for which trials are funded shall be deposited into the state general fund. For purposes of this subsection, intellectual property rights and other commercial rights arising from the clinical trials conducted under this Code section shall include any of the following as related to such trials:
(1) Intellectual property, technology, and inventions;
(2) Patents, trademarks, and licenses;
(3) Proprietary and confidential information;
(4) Trade secrets, data, and databases;
(5) Tools, methods, and processes;
(6) Treatment models or techniques;
(7) Administration protocols; and
(8) Works of authorship.
(e) The commissioner shall prepare an accounting of the funds expended pursuant to this Code section during the most recently completed fiscal year to be reported to the Office of Planning and Budget, the House Budget and Research Office, and the Senate Budget and Evaluation Office by January 1 of each year.
(f) The department shall submit to the General Assembly a report on the progress of the clinical trials and their related financial status conducted under this Code section not later than December 1 of each year. Such report shall include information verifying expenditures of state funds and required matching funds.
(g) Nothing in this Code section shall be construed to preclude a physician from administering ibogaine in accordance with federal law and state law."
SECTION 3.
(a) This Act shall become effective only if funds are specifically appropriated for purposes of this Act in an appropriations Act enacted by the General Assembly.
(b) If funds are so appropriated, then this Act shall become effective on the later of:
(1) The date on which such appropriations Act becomes effective; or
(2) The beginning date of the fiscal year for which such appropriations are made.
(c) If funds are not appropriated by July 1, 2029, as described in this section, this Act shall stand repealed.
SECTION 4.
All laws and parts of laws in conflict with this Act are repealed.