Montana’s legislature has legalized so-called “experimental treatment centers,” allowing clinics to administer FDA-unapproved therapies—ranging from peptide and gene injections to NAD+ infusions—for longevity outside the typical trial framework.
Key points
- Montana law licenses clinics to administer Phase 1-only anti-aging therapies without FDA Phase 2/3 approval.
- Therapies include NAD+ infusions, peptide/gene protocols targeting follistatin and klotho proteins.
- Clinics must allocate 2% of profits to low-income patients, expanding access beyond terminally ill groups.
Why it matters: By cutting regulatory delays, this law could accelerate human testing of novel longevity modalities, but raises critical safety and equity considerations.
Q&A
- What is an experimental treatment center?
- How does NAD+ therapy work?
- What are follistatin and klotho therapies?
- What regulatory phases do these treatments skip?
- Are these treatments covered by insurance?