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Current as of January 01, 2021 | Updated by FindLaw Staff
A patient shall be eligible for treatment with an investigational drug, biological product, or device if the patient has:
(1) A terminal illness that is attested to by the patient's treating health care provider;
(2) Considered all other treatment options currently approved by the United States Food and Drug Administration;
(3) Received a recommendation from the patient's treating health care provider for an investigational drug, biological product, or device;
(4) Given written informed consent for the use of the investigational drug, biological product, or device; and
(5) Documentation from the treating health care provider that the patient meets the requirements of this section.
Cite this article: FindLaw.com - Kentucky Revised Statutes Title XVIII. Public Health § 217.5403.Eligibility requirements for treatment with investigational drug, biological product, or device - last updated January 01, 2021 | https://codes.findlaw.com/ky/title-xviii-public-health/ky-rev-st-sect-217-5403/
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