Referred to the Subcommittee on Health and Environment.
Congressional Research Service
Official summary
Version 00 · Introduced in House · Mar 21, 1996
Terminally Ill Access to Treatment Act of 1996 - Directs the Secretary of Health and Human Services to approve, for treating the terminally ill only, drugs and devices that have not received final approval from the Food and Drug Administration (FDA) and that have not been shown to be unsafe. Declares that it is not illegal for a health care practitioner to administer a drug or device approved under this Act to a terminally ill patient if the practitioner has notified the patient that the drug or device is not FDA-approved and is experimental and if the practitioner has received written approval from the patient or the patient's representative. Requires a practitioner to report acute harm done by such a drug or device. Requires the Secretary to give public notice of the benefits and harm caused by such a drug or device.
No related bills are listed in this snapshot. This does not establish whether the proposal has appeared in earlier Congresses.
Source last updated: Jun 3, 2026. Consult Congress.gov for the current record.
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