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152.21 THC THERAPEUTIC RESEARCH ACT.
    Subdivision 1. Findings and purpose. The legislature finds that scientific literature
indicates promise for delta-9-tetrahydro-cannabinol (THC), the active component of marijuana,
in alleviating certain side effects of cancer chemotherapy under strictly controlled medical
circumstances.
The legislature also finds that further research and strictly controlled experimentation
regarding the therapeutic use of THC is necessary and desirable. The intent of this section is to
establish an extensive research program to investigate and report on the therapeutic effects of
THC under strictly controlled circumstances in compliance with all federal laws and regulations
promulgated by the federal Food and Drug Administration, the National Institute on Drug Abuse
and the Drug Enforcement Administration. The intent of the legislature is to allow this research
program the greatest possible access to qualified cancer patients residing in Minnesota who meet
protocol requirements. The establishment of this research program is not intended in any manner
whatsoever to condone or promote the illicit recreational use of marijuana.
    Subd. 2. Definitions. For purposes of this section, the following terms shall have the
meanings given.
(a) "Commissioner" means the commissioner of health.
(b) "Marijuana" means marijuana as defined in section 152.01, subdivision 9, and
delta-9-tetrahydro-cannabinol (THC), tetrahydrocannabinols or a chemical derivative of
tetrahydrocannabinols, and all species of the genus Cannabis.
(c) "Principal investigator" means the individual responsible for the medical and scientific
aspects of the research, development of protocol, and contacting and qualifying the clinical
investigators in the state.
(d) "Clinical investigators" means those individuals who conduct the clinical trials.
(e) "Sponsor" means that individual or organization who, acting on behalf of the state, has
the total responsibility for the state program.
    Subd. 3. Research grant. The commissioner of health shall grant funds to the principal
investigator selected by the commissioner pursuant to subdivision 4 for the purpose of conducting
a research program under a protocol approved by the FDA regarding the therapeutic use of oral
THC and other dosage forms, if available, according to the guidelines and requirements of the
federal Food and Drug Administration, the Drug Enforcement Administration and the National
Institute on Drug Abuse. The commissioner shall ensure that the research principal investigator
complies with the requirements of subdivision 5. The commissioner may designate the principal
investigator as the sponsor.
    Subd. 4. Principal investigator. Within three months of April 25, 1980, the commissioner
shall, in consultation with a representative chosen by the state Board of Pharmacy and a
representative chosen by the state Board of Medical Examiners, select a person or research
organization to be the principal investigator of the research program.
    Subd. 5. Duties. The principal investigator shall:
(1) Apply to the Food and Drug Administration for a notice of "Claimed Investigational
Exemption for a New Drug (IND)" pursuant to the Federal Food, Drug and Cosmetic Act,
United States Code, title 21, section 301, et seq., and shall comply with all applicable laws and
regulations of the federal Food and Drug Administration, the Drug Enforcement Administration,
and the National Institute on Drug Abuse in establishing the program;
(2) Notify every oncologist in the state of the program, explain the purposes and requirements
of the program to them, provide on request each of them with a copy of the approved protocol
which shall include summaries of current papers in medical journals reporting on research
concerning the safety, efficacy and appropriate use of THC in alleviating the nausea and emetic
effects of cancer chemotherapy, and provide on request each of them with a bibliography of
other articles published in medical journals;
(3) Allow each oncologist (clinical investigator) in the state who meets or agrees to meet all
applicable federal requirements for investigational new drug research and who so requests to be
included in the research program as a clinical investigator to conduct the clinical trials;
(4) Provide explanatory information and assistance to each clinical investigator in
understanding the nature of therapeutic use of THC within program requirements, including the
informed consent document contained in the protocol, informing and counseling patients involved
in the program regarding the appropriate use and the effects of therapeutic use of THC;
(5) Apply to contract with the National Institute on Drug Abuse for receipt of dosage
forms of THC, fully characterized as to contents and delivery to the human system, pursuant to
regulations promulgated by the National Institute on Drug Abuse, and the federal Food and Drug
Administration. The principal investigator shall ensure delivery of the THC dosages to clinical
investigators as needed for participation in the program;
(6) Conduct the research program in compliance with federal laws and regulations
promulgated by the federal Food and Drug Administration, the Drug Enforcement Administration,
the National Institute on Drug Abuse, and the purposes and provisions of this section;
(7) Submit periodic reports as determined by the commissioner on the numbers of oncologists
and patients involved in the program and the results of the program;
(8) Submit reports on intermediate or final research results, as appropriate, to the major
scientific journals in the United States; and
(9) Otherwise comply with the provisions of this section.
    Subd. 6. Exemption from criminal sanctions. For the purposes of this section, the
following are not violations under this chapter:
(1) use or possession of THC, or both, by a patient in the research program;
(2) possession, prescribing use of, administering, or dispensing THC, or any combination of
these actions, by the principal investigator or by any clinical investigator; and
(3) possession or distribution of THC, or both, by a pharmacy registered to handle schedule I
substances which stores THC on behalf of the principal investigator or a clinical investigator.
THC obtained and distributed pursuant to this section is not subject to forfeiture under
sections 609.531 to 609.5316.
For the purposes of this section, THC is removed from schedule I contained in section
152.02, subdivision 2, and inserted in schedule II contained in section 152.02, subdivision 3.
    Subd. 7. Citation. This section may be cited as the "THC Therapeutic Research Act."
History: 1980 c 614 s 93; 1988 c 665 s 2; 1989 c 290 art 3 s 23; 1997 c 7 art 2 s 22