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MN HF4064

Bill

Status

Introduced

3/9/2026

Primary Sponsor

Liz Reyer

Click for details

Origin

House of Representatives

94th Legislature 2025-2026

AI Summary

  • Commissioner of Health must conduct a comprehensive study on Minnesota's capacity for rare disease cell and gene therapy research, development, delivery, and access, in consultation with the University of Minnesota and the Minnesota Rare Disease Advisory Council

  • Study must assess 10 areas including: other states' capabilities, clinical trial capacity, biomanufacturing opportunities, health system delivery readiness, workforce needs, payment policies under Medicaid and commercial insurers, regulatory barriers, and health equity issues for rural and underserved communities

  • Commissioner must seek input from patients, caregivers, advocacy groups, health care providers, academic institutions, payers, pharmacy benefit managers, and biotechnology/pharmaceutical industries

  • Report due to the legislature by January 1, 2028, with findings, short-term and long-term recommendations for state investments and policy changes, and identification of federal funding opportunities and public-private partnerships

  • One-time general fund appropriation in fiscal year 2027 (amount unspecified in bill text) available through June 30, 2028

Legislative Description

Commissioner of health directed to study and report on activities to support innovations in cell and gene therapy to treat rare diseases, report required, and money appropriated.

Last Action

Introduction and first reading, referred to Health Finance and Policy

3/9/2026

Committee Referrals

Health Finance & Policy3/9/2026

Full Bill Text

No bill text available