Bill Text For HB4293 - Introduced

 1|                          STATE OF OKLAHOMA                            |
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 2|             2nd Session of the 60th Legislature (2026)                |
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 3|HOUSE BILL 4293                      By: Pae                           |
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 6|                            AS INTRODUCED                              |
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 7|       An Act relating to controlled dangerous substances;             |
  |       creating the Veterans Mental Health Innovation Act;             |
 8|       authorizing certain entities to conduct scientific              |
  |       research and clinical trials related to ibogaine;               |
 9|       specifying certain uses for which scientific research           |
  |       or clinical trials are authorized; limiting number of           |
10|       memoranda of agreement that universities or                     |
  |       institutions of higher education may enter into;                |
11|       imposing requirements with respect to studies;                  |
  |       requiring registration with the State Department of             |
12|       Health and the Oklahoma Department of Agriculture,              |
  |       Food, and Forestry; prescribing requirements for                |
13|       registration information; providing for specified               |
  |       nonrefundable fees; requiring additional registration           |
14|       with the Oklahoma State Bureau of Narcotics and                 |
  |       Dangerous Drugs Control; stipulating duration of                |
15|       registration; requiring certain notification of                 |
  |       change of facility location; requiring written                  |
16|       certifications for clinical trial participants;                 |
  |       prescribing content of written certifications;                  |
17|       providing for expiration of certifications; providing           |
  |       immunity to persons conducting or participating in              |
18|       research or clinical trials; requiring submission of            |
  |       written reports by certain date; providing for                  |
19|       confidentiality of certain personal information;                |
  |       requiring specified agencies to maintain                        |
20|       confidentiality with respect to information;                    |
  |       directing promulgation of rules; providing for                  |
21|       codification; and providing an effective date.                  |
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   Req. No. 15634                                                  Page 1
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 1|BE IT ENACTED BY THE PEOPLE OF THE STATE OF OKLAHOMA:                  |
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 2|    SECTION 1.     NEW LAW     A new section of law to be codified     |
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 3|in the Oklahoma Statutes as Section 2-810 of Title 63, unless there    |
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 4|is created a duplication in numbering, reads as follows:               |
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 5|    A.  This act shall be known and may be cited as the "Veterans      |
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 6|Mental Health Innovation Act".                                         |
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 7|    B.  The purpose of this act is to allow states and commonwealths   |
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 8|to join a multistate consortium to advance research on ibogaine as     |
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 9|medical treatment.                                                     |
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10|    SECTION 2.     NEW LAW     A new section of law to be codified     |
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11|in the Oklahoma Statutes as Section 2-811 of Title 63, unless there    |
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12|is created a duplication in numbering, reads as follows:               |
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13|    A.  A university or other institution of higher education          |
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14|located in this state, or a research facility that has entered into    |
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15|a memorandum of agreement with a university or institution of higher   |
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16|education located in this state, may conduct scientific research on    |
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17|ibogaine for the treatment of persons eighteen (18) years of age or    |
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18|older who experience any of the following medical conditions:          |
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19|    1.  Posttraumatic stress disorder;                                 |
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20|    2.  Treatment-resistant/refractory depression;                     |
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21|    3.  Treatment-resistant/refractory anxiety;                        |
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22|    4.  Treatment-resistant/refractory obsessive-compulsive            |
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23|disorder;                                                              |
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24|    5.  Traumatic brain injury;                                        |
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   Req. No. 15634                                                  Page 2
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 1|    6.  Early-stage dementia;                                          |
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 2|    7.  Palliative care;                                               |
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 3|    8.  End-of-life care;                                              |
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 4|    9.  Opioid use disorder; or                                        |
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 5|    10.  Moderate to severe chronic pain.                              |
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 6|    B.  The university or institution of higher education may enter    |
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 7|into no more than one memorandum of agreement with a research          |
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 8|facility for the purposes of conducting scientific research under      |
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 9|this section.                                                          |
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10|    C.  In conducting such scientific research as described in         |
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11|subsection B of this section, the studies shall:                       |
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12|    1.  Study the therapeutic efficacy of using ibogaine in the        |
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13|treatment of the medical conditions listed in subsection B of this     |
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14|section;                                                               |
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15|    2.  Review the current literature regarding:                       |
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16|         a.    the safety and efficacy of using ibogaine in the        |
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17|              treatment of the medical conditions listed in            |
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18|              subsection C of this section, and                        |
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19|         b.    the access persons have to ibogaine for the treatment   |
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20|              of the medical conditions listed in subsection A of      |
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21|              this section; and                                        |
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22|    3.  Examine the science of cultivation, synthesis, extraction,     |
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23|and processing of ibogaine as well as any other naturally occurring    |
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24|source organisms of these molecules.                                   |
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   Req. No. 15634                                                  Page 3
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 1|    D.  1.  Eligible entities as described in subsection A of this     |
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 2|section shall register with the State Department of Health and the     |
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 3|Oklahoma Department of Agriculture, Food, and Forestry prior to and    |
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 4|for the purposes of growing, studying, processing, or dispensing       |
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 5|ibogaine-containing Tabernanthe iboga plant, or studying,              |
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 6|extracting, synthesizing, or dispensing ibogaine.  The registration    |
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 7|submission information shall include:                                  |
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 8|         a.    the name and address of the research facility,          |
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 9|         b.    a prospectus approved by a university or other          |
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10|              institution of higher education, and                     |
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11|         c.    certification from the institutional review board of    |
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12|              the university or institution of higher education if     |
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13|              human trials are part of the research.                   |
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14|    2.  By registering, the registrant acknowledges and agrees that:   |
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15|         a.    the information contained in the registration           |
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16|              submissions may be provided to law enforcement           |
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17|              agencies, and                                            |
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18|         b.    the registrant shall submit an annual report            |
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19|              detailing compliance with annual regulation              |
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20|              requirements.                                            |
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21|    3.  The State Department of Health shall collect a one-time,       |
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22|nonrefundable fee of Five Hundred Dollars ($500.00) from the           |
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23|registrant at the time of registration and the Oklahoma Department     |
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24|of Agriculture, Food, and Forestry shall collect a one-time            |
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   Req. No. 15634                                                  Page 4
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 1|nonrefundable fee of One Hundred Dollars ($100.00) from the            |
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 2|registrant at the time of registration.  The registrant shall, upon    |
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 3|completion of registration with the State Department of Health and     |
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 4|the Oklahoma Department of Agriculture, Food, and Forestry, register   |
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 5|with the Oklahoma State Bureau of Narcotics and Dangerous Drugs        |
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 6|Control as provided by Section 2-301 et seq. of Title 63 of the        |
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 7|Oklahoma Statutes annually for as long as the research remains         |
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 8|active.                                                                |
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 9|    4.  Registration under this subsection is valid for one (1)        |
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10|year, effective upon confirmation and receipt of all registrations     |
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11|required by this subsection.  Notwithstanding the registration fee     |
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12|listed in Section 2-303 of Title 63 of the Oklahoma Statutes, the      |
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13|registration required by this subsection shall satisfy and supersede   |
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14|all other registration and reporting requirements otherwise imposed    |
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15|by state law.                                                          |
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16|    5.  Should the registrant change facility locations for the        |
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17|cultivation, testing, synthesis, storage, or dispensing of ibogaine,   |
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18|it shall report such changes within fourteen (14) business days to     |
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19|the State Department of Health, the Oklahoma Department of             |
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20|Agriculture, Food, and Forestry, and the Oklahoma State Bureau of      |
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21|Narcotics and Dangerous Drugs Control.                                 |
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22|    E.  1.  A written certification shall be issued to persons         |
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23|qualifying for participation in the pilot program described in this    |
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   Req. No. 15634                                                  Page 5
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 1|section by a physician participating in the pilot program.  The        |
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 2|written certification shall contain the following:                     |
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 3|         a.    the name, address, and telephone number of the          |
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 4|              issuing physician,                                       |
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 5|         b.    the name and address of the patient to whom the         |
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 6|              written certification is issued,                         |
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 7|         c.    the date on which the written certification was made,   |
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 9|         d.    the signature of the physician,                         |
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10|         e.    the quantity of ibogaine to be dispensed, and           |
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11|         f.    the form of ibogaine to be dispensed.                   |
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12|    2.  The written certification issued under this subsection shall   |
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13|expire one (1) year after its issuance unless the written              |
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14|certification specifies an earlier date of expiration.                 |
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15|    F.  1.  A scientific researcher or physician operating under a     |
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16|valid registration issued in accordance with this section shall not    |
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17|be subject to arrest, prosecution, or any civil or administrative      |
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18|penalty for the possession, cultivation, synthesis, extraction, or     |
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19|distribution of ibogaine insofar as the scientific researcher's or     |
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20|physician's conduct is in compliance with the provisions of this       |
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21|section.                                                               |
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22|    2.  A patient participating in the pilot program under a valid     |
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23|written certification issued in accordance with this section shall     |
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24|not be subject to arrest, prosecution, or any civil or                 |
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   Req. No. 15634                                                  Page 6
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 1|administrative penalty for the use or possession of ibogaine insofar   |
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 2|as the patient's conduct is in compliance with the provisions of       |
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 3|this section.                                                          |
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 4|    3.  In any prosecution involving possession of ibogaine as those   |
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 5|terms are specified in subsection C of Section 2-204 of Title 63 of    |
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 6|the Oklahoma Statutes, it shall be an affirmative defense if a         |
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 7|person can demonstrate by clear and convincing evidence that he or     |
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 8|she has one or more of the qualifying medical conditions or            |
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 9|circumstances listed in subsection B of this section.  This            |
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10|subsection shall not be understood to be the decriminalization of      |
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11|ibogaine.                                                              |
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12|    G.  Researching entities shall submit a final written report to    |
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13|the President Pro Tempore of the Oklahoma State Senate and the         |
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14|Speaker of the Oklahoma House of Representatives containing the        |
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15|results of the studies conducted under this section and any            |
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16|recommendations for legislative or other actions not later than        |
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17|December 1, 2029.                                                      |
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18|    H.  Researching entities shall ensure any protected health         |
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19|information collected during the pilot program done in accordance      |
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20|with this section does not personally identify any individual.         |
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21|    I.  The State Department of Health, the Oklahoma Department of     |
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22|Agriculture, Food, and Forestry, the Oklahoma State Bureau of          |
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23|Narcotics and Dangerous Drugs Control, and any other state agency      |
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24|with access to the research programs authorized by this section        |
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   Req. No. 15634                                                  Page 7
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 1|shall not release or allow to be released through inaction any         |
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 2|protected health information.  The protected health information of     |
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 3|pilot program participants shall be exempt from the Oklahoma Open      |
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 4|Records Act.                                                           |
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 5|    J.  The State Commissioner of Health, the State Board of           |
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 6|Agriculture, and the Director of the Oklahoma State Bureau of          |
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 7|Narcotics and Dangerous Drugs Control shall promulgate rules           |
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 8|necessary to implement the program authorized in this section.         |
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 9|    K.  On the condition that ibogaine is approved by the Untied       |
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10|States Food and Drug Administration to treat a medical condition:      |
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11|    1.  A licensed physician shall prescribe ibogaine for a patient;   |
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12|and                                                                    |
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13|    2.  A licensed physician shall supervise the administration of     |
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14|ibogaine at a hospital or other licensed health care facility to       |
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15|ensure the patient's safety while the patient is under the influence   |
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16|of ibogaine.                                                           |
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17|    SECTION 3.  This act shall become effective November 1, 2026.      |
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19|    60-2-15634     TKR    01/12/26                                     |
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   Req. No. 15634                                                  Page 8
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