West Virginia law defines which seriously ill patients qualify as eligible and what risks, care changes, and possible costs their written consent must explain.
The law defines eligible patients as seriously ill people who have considered approved options and have a physician’s recommendation, written consent, and documentation. Hospital inpatients are excluded.
Written consent must explain possible treatment outcomes, including worsened symptoms or death coming sooner, and warn that care or related bills may be affected.
The law defines which patients count as eligible and which treatments count as investigational. The definitions cover patients with life-threatening or severely debilitating illnesses and drugs, biological products, or devices. A patient must have a life-threatening or severely debilitating illness attested to by a treating physician, have considered FDA-approved options, receive a physician’s recommendation, and have the required written consent and physician documentation. A parent or legal guardian may consent for a minor or a person unable to consent. A person being treated as a hospital inpatient is excluded. The treatment definition covers products that completed phase one of a clinical trial but lack FDA approval for general use, and products made exclusively for one patient based on that person’s genetic profile. The act took effect June 12, 2026, 90 days after passage.
The law requires written consent to explain treatment risks, costs, and possible effects on care. These consent requirements apply when an eligible patient seeks to use an investigational drug, biological product, or device. The document must be signed by the patient and attested to by the patient’s physician and a witness. It must explain approved treatments, identify the proposed treatment, and describe possible outcomes, including worsened symptoms or death coming sooner. It must explain that insurers and providers may not have to pay for related care; hospice eligibility may be withdrawn and later restored if requirements are met; in-home care may be denied; and the patient or estate may owe related expenses unless a manufacturer contract says otherwise. The act took effect June 12, 2026, 90 days after passage.
No hearings or votes scheduled.