Study summary
Methylone, a relative of MDMA, was put on a fast FDA track
What was tested
Methylone (TSND-201), a shorter-acting chemical relative of MDMA given in supervised sessions without a structured therapy program.
What they found
- The FDA granted a national priority voucher in April 2026, which shortens review once an application is filed.
- Phase 3 began after positive mid-stage results.
- No application has been filed yet.
What it means
The PTSD drug most likely to reach an FDA decision next.
Last reviewed 2026-11-14 by the Find a Trial editorial team.
Information on this page is for educational purposes and is not medical advice.
Always consult qualified healthcare professionals about clinical trial participation.