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Enacted

Utah expands patient access to investigational drugs and medical devices under Right to Try law

Original title: Right to Try Amendments

Last action · March 18, 2026: Governor SignedSponsors: Chris Wilson and 1 other

Introduced
Committee
Floor Vote
Passed
Law

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Public stanceCommunity reactions are separate from the official record and reporting.

What This Bill Does

Utah law now allows eligible patients with severe or life-threatening conditions to obtain s and devices under expanded circumstances, while requiring manufacturers to submit annual safety and usage reports to the Legislature starting May 6, 2026.

Why it matters

Patients facing debilitating illnesses gain wider legal pathways to unapproved medical treatments, while medical manufacturers face a mandatory annual reporting requirement regarding patient outcomes and adverse events.

Who It Affects

Groups the bill's text affects, as described in the record. Being affected is not a position for or against it.

Directly affected

Eligible patients

Patients diagnosed with severe, debilitating, or terminal conditions gain expanded statutory access to investigational drugs and devices.

Directly affected

Investigational drug and device manufacturers

Manufacturers providing unapproved treatments to Utah residents must compile and submit annual adverse outcome and patient usage data to a legislative committee.

Directly affected

Physicians

Licensed medical and osteopathic physicians are authorized to diagnose qualifying conditions and determine patient eligibility for investigational treatments.

Key Facts

You don't have to trust us. Each fact below is taken straight from the official document - click any one to see the exact passage, highlighted in the original.

Frequently Asked Questions

Who qualifies to receive an investigational drug or device under this law?
An eligible patient is an individual diagnosed with a terminal illness or a condition that presents a substantial, severely debilitating, or life-threatening risk, provided they have explored conventional therapy options with no satisfactory comparable treatment.
What information must manufacturers report to the state?
Manufacturers must report the number of patients treated, each eligible illness being treated, adverse outcomes likely attributable to the product, and any other relevant information.
Are all manufacturers required to submit the annual report?
No. Manufacturers are exempt from the reporting requirement if the patient receiving the or device was part of a formal clinical investigation conducted under 21 C.F.R. Part 312 or 812.

What else do you want to know?

News Coverage

No news coverage found yet. Articles are indexed twice daily.

Where This Stands

Current status: Signed into law.

Procedural history

49 actions
  1. Mar 18, 2026Lieutenant Governor's office for filingEnrolled
    Governor Signed
  2. Mar 13, 2026Senate
    Senate/ to Governor
  3. Mar 13, 2026Senate
    Senate/ received enrolled bill from Printing
  4. Mar 11, 2026Senate
    Senate/ enrolled bill to Printing
  5. Mar 11, 2026Senate Secretary
    Enrolled Bill Returned to House or Senate
  6. Mar 6, 2026Legislative Research and General Counsel / Enrolling
    Draft of Enrolled Bill Prepared
Show 43 earlier actions
  1. Mar 6, 2026Legislative Research and General Counsel / Enrolling
    Bill Received from Senate for Enrolling
  2. Mar 6, 2026Senate
    Senate/ signed by President/ sent for enrolling
  3. Mar 6, 2026Senate
    Senate/ received from House
  4. Mar 5, 2026House
    House/ to Senate
  5. Mar 5, 2026House
    House/ signed by Speaker/ returned to Senate
  6. Mar 5, 2026HouseFloor
    House/ passed 3rd reading
  7. Mar 5, 2026House
    House/ 3rd reading
  8. Mar 2, 2026House
    House/ 2nd reading
  9. Mar 2, 2026House
    House/ committee report favorable
  10. Feb 27, 2026House
    House Comm - Favorable Recommendation
  11. Feb 25, 2026HouseCommittee
    House/ to standing committee
  12. Feb 24, 2026HouseIntroduced
    House/ 1st reading (Introduced)
  13. Feb 23, 2026House
    House/ received from Senate
  14. Feb 23, 2026Senate
    Senate/ to House
  15. Feb 23, 2026SenateFloor
    Senate/ passed 3rd reading
  16. Feb 23, 2026Senate
    Senate/ uncircled
  17. Feb 23, 2026Released
    LFA/ fiscal note publicly available for SB0222S02
  18. Feb 23, 2026Version Sponsor
    LFA/ fiscal note sent to sponsor for SB0222S02
  19. Feb 23, 2026Senate
    Senate/ circled
  20. Feb 23, 2026Senate
    Senate/ substituted
  21. Feb 23, 2026Senate
    Senate/ 3rd reading
  22. Feb 23, 2026Legislative Fiscal Agency
    LFA/ bill sent to agencies for fiscal input for SB0222S02
  23. Feb 23, 2026Legislative Fiscal Analyst
    LFA/ bill assigned to staff for fiscal analysis for SB0222S02
  24. Feb 20, 2026SenateFloor
    Senate/ passed 2nd reading
  25. Feb 20, 2026Senate
    Senate/ substituted
  26. Feb 20, 2026Senate
    Senate/ 2nd reading
  27. Feb 19, 2026Released
    LFA/ fiscal note publicly available for SB0222S01
  28. Feb 18, 2026Version Sponsor
    LFA/ fiscal note sent to sponsor for SB0222S01
  29. Feb 17, 2026Legislative Fiscal Agency
    LFA/ bill sent to agencies for fiscal input for SB0222S01
  30. Feb 17, 2026Legislative Fiscal Analyst
    LFA/ bill assigned to staff for fiscal analysis for SB0222S01
  31. Feb 4, 2026Senate
    Senate/ placed on 2nd Reading Calendar
  32. Feb 4, 2026Senate
    Senate/ committee report favorable
  33. Feb 3, 2026Senate
    Senate Comm - Favorable Recommendation
  34. Feb 2, 2026SenateCommittee
    Senate/ to standing committee
  35. Feb 2, 2026Senate
    Senate/ received fiscal note from Fiscal Analyst
  36. Feb 2, 2026Released
    LFA/ fiscal note publicly available for SB0222
  37. Feb 2, 2026Version Sponsor
    LFA/ fiscal note sent to sponsor for SB0222
  38. Jan 30, 2026SenateIntroduced
    Senate/ 1st reading (Introduced)
  39. Jan 29, 2026Senate
    Senate/ received bill from Legislative Research
  40. Jan 29, 2026Legislative Fiscal Agency
    LFA/ bill sent to agencies for fiscal input for SB0222
  41. Jan 29, 2026Legislative Fiscal Analyst
    LFA/ bill assigned to staff for fiscal analysis for SB0222
  42. Jan 29, 2026Legislative Research and General Counsel
    Numbered Bill Publicly Distributed
  43. Jan 29, 2026Legislative Research and General Counsel
    Bill Numbered but not Distributed

Version history

Only one version on file - nothing to compare yet. As later stages (committee substitute, engrossed, enrolled) are captured, the redline appears here.

View official text →

Lobbying Activity

No state lobbying filings in our records match this bill. Federal lobbying reports (LDA) cover Congress, so they are not listed on state bills.

Full breakdown

Who this bill affects and the strongest case for and against it, written only from the bill’s own text.

Sponsors

Discoveries

1 pattern noticed across the record

Patterns POLISCOPE noticed across the record. These are observations to investigate, not conclusions.

policy shift98% confidence

Expansion of Right to Try Framework

The state shifts from strictly terminal illness limitations to encompassing broader severely debilitating or life-threatening conditions.

Connected Entities

Health and Human Services Interim Committee, United States Food and Drug Administration
OrganizationHealth and Human Services Interim Committee“Recipient of annual manufacturer reports on investigational drug and device use.”Map →
OrganizationUnited States Food and Drug Administration“Regulates Phase 1 testing and clinical investigations for drugs and devices.”Map →

Sources

Analysis Score

0–100
  • Significance75
    How much this matters to a regular citizen
  • Controversy25
    Intensity of disagreement among stakeholders
  • Entertainment5
    Compellingness for a non-policy-wonk reader
  • Buzz35
    Current news / social attention level

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