All Roll Calls
Yes: 310 • No: 0
Sponsored By: Paul Bettencourt (Republican), Ken King
Signed by Governor
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6 provisions identified: 2 benefits, 1 costs, 3 mixed.
Beginning September 1, 2025, Texas patients can request experimental drugs, biologic products, or devices made only for their genetic profile. Patients must have a life-threatening illness or one causing major, lasting harm, and must have considered all FDA-approved treatments. A treating doctor must confirm eligibility and recommend treatment based on genetic or other specified biological information. Access runs through facilities operating under a federal assurance protecting human subjects; manufacturers and facilities can decline, and hospitals need not add services. State officials cannot block access that follows the law, but providers can still give advice consistent with medical standards.
Beginning September 1, 2025, heirs are protected if a patient dies while receiving treatment under this law. They are not liable for unpaid treatment debt or debt caused by lost health coverage due to the treatment. This protection does not erase separate liability of the patient or estate.
Beginning September 1, 2025, participating facilities and manufacturers may provide treatment free or charge manufacturing and related costs. The law sets no price. Required consent states that patients bear treatment-related expenses, potentially extending to their estates, unless a manufacturer contract provides otherwise. Health plans, plan administrators, and government agencies may cover treatment and related care, but this law creates no payment duty. Existing legal and contract duties remain, including insurance and clinical-trial coverage requirements.
Beginning September 1, 2025, patients need written informed consent, confirmed in writing by a doctor and witness, before treatment. A parent, guardian, managing conservator, or designated agent can consent for a minor or patient lacking mental capacity. Consent must describe approved treatments, the patient's statement that recognized treatments are unlikely to prolong life, and the proposed treatment. It must explain best, worst, and most likely outcomes, including harm or earlier death, possible lack of insurance payment, and patient expense liability that may reach the estate. It must also warn that hospice eligibility may end when treatment starts and may return after treatment ends if hospice requirements are met.
Beginning September 1, 2025, Texas licensing boards cannot punish providers solely for recommending access to these personalized experimental treatments. The Health and Human Services Commission also cannot harm a provider's Medicaid participation solely for that recommendation. These protections do not prevent action on other grounds.
Beginning September 1, 2025, this law creates no new private lawsuit right for treatment harm against manufacturers or others involved in care. That limit applies when they follow the law in good faith and use reasonable care. It does not say that all other legal claims are barred.
Paul Bettencourt
Republican • Senate
Ken King
House
There are no cosponsors for this bill.
All Roll Calls
Yes: 310 • No: 0
House vote • 5/20/2025
Record vote
Yes: 147 • No: 0
House vote • 5/19/2025
Record vote
Yes: 143 • No: 0
Senate vote • 4/10/2025
Record vote
Yes: 0 • No: 0
Senate vote • 4/10/2025
Record vote
Yes: 0 • No: 0
House vote • Unknown
Committee vote: Public Health
Yes: 11 • No: 0
Senate vote • Unknown
Committee vote: Health & Human Services
Yes: 9 • No: 0
Effective on 9/1/25
Signed by the Governor
Sent to the Governor
Signed in the House
Signed in the Senate
Reported enrolled
House passage reported
Record vote (RV#3009)
Passed
Read 3rd time
Statement(s) of vote recorded in Journal
Record vote (RV#2939)
Passed to 3rd reading
Read 2nd time
Placed on General State Calendar
Considered in Calendars
Corrected committee report sent to Calendars
Corrected comm. report distributed
Corrected com rept filed w/ Comte Coordinator
Committee report sent to Calendars
Committee report distributed
Comte report filed with Committee Coordinator
Reported favorably w/o amendment(s)
Considered in formal meeting
Referred to Public Health
Engrossed
Enrolled
House Committee Report
Introduced
Senate Committee Report
SB 785, Relating to the regulation of new HUD-code manufactured housing.
SB 650, Relating to requiring the use of electronically readable information to verify a purchaser's age in the retail sale of alcoholic beverages.
SB 646, Relating to repayment of certain mental health professional education loans.
SB 25, Relating to health and nutrition standards to promote healthy living, including requirements for food labeling, primary and secondary education, higher education, and continuing education for certain health care professionals; authorizing a civil penalty.
HB 4325, Relating to civil liability for prohibited barratry.
HB 4042, Relating to the applicability of certain safety provisions and regulatory fees administered by the Railroad Commission of Texas to gas distribution pipelines.