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Conferees accept federal definition of "life-threatening" in HB 701-FN but leave eligibility, provider scope and conscience protections unresolved

3847161 · June 16, 2025
AI-Generated Content: All content on this page was generated by AI to highlight key points from the meeting. For complete details and context, we recommend watching the full video. so we can fix them.

Summary

The Committee of Conference on HB 701-FN agreed to adopt federal language (citing FDA guidance) to define "life-threatening" or "terminal" illness for access to investigational treatments, but deferred decisions about eligible facilities, which licensed providers may participate, and conscience protections for physicians.

Conferees on House Bill 701-FN, a bill addressing access to investigational drugs, biologics and devices for patients with terminal illnesses, agreed to adopt federal language for defining "life-threatening" or "terminal" illness but did not resolve three major outstanding issues: the definition of an eligible facility, which licensed providers may offer investigational treatments, and legal protections for physicians who decline to provide requested treatments.

Senators and representatives spent substantial time debating the definition of a terminal or life-threatening condition. Several conferees recommended relying on federal standards. One conferee read the U.S. Food and Drug Administration regulation at 21 C.F.R. § 312.81, which the participants said defines "life-threatening" to include diseases where "the likelihood of death is high unless the course of…

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