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Committee hears "right to try" bill for individualized treatments; regulator urges clarity on consent and estate liability
Summary
The committee heard Senate Bill 250, which would create a pathway for patients with life‑threatening or severely debilitating illnesses to obtain individualized investigational treatments (bespoke therapies based on a patient’s genetic profile). Supporters said the bill modernizes right‑to‑try law for genomic medicine; the Kansas State Board of
The House Committee on Health and Human Services heard Senate Bill 250, a proposal to enact a “right to try for individualized treatments” that would allow manufacturers to provide an individualized investigational treatment to an eligible patient — defined in the bill as someone with a life‑threatening or severely debilitating illness who has exhausted other FDA‑approved options and has a physician recommendation.
Carly (committee staff) summarized the bill’s provisions, including definitions, a manufacturer’s option (rather than requirement) to provide treatment, provisions that allow but do not require insurers or governmental payers to cover costs, and language shielding manufacturers and providers from a private cause of action in some circumstances. The staff summary noted that the bill passed the Senate…
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