An Evaluation of the Long-term Efficacy and Safety of Methylone for the Treatment of PTSD
Completed · Phase 2
Conditions studied: Post Traumatic Stress Disorder
In brief
This is an extension study of participants who previously completed a Transcend-sponsored clinical trial evaluating TSND-201 as a treatment for PTSD. Participants will be followed for up to 52 weeks. During the 52 week period, PTSD symptoms and safety will be assessed monthly. Participants' PTSD symptoms will be assessed at each observational visit and if criteria for Relapse has been met, participants may be eligible to receive a course of TSND-201 treatment.
Key facts
- Study ID
- NCT06237426
- Run by
- Transcend Therapeutics
- People needed
- 44
- Starts
- 2024-03-06
- Expected to finish
- 2025-10-06
- Last updated by the study team
- 2025-11-25
Who can join
Age: 18 and older, up to 71. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Participation in and successful completion of a prior Transcend-sponsored clinical trial with TSND-201.
- Agree to not participate in any other interventional clinical trials for the duration of this study.
- Willing and able to provide informed consent.
You may not qualify if…
- Had significant deviation(s)/non-compliance in parent study in the opinion of the Investigator which would deem them unsuitable for participation.
- Change or development of any physical or psychological finding that would make participant unsuitable for study.
Where it is running
- Mountain View Clinical Research — Denver, Colorado, United States
- Sunstone Medical — Rockville, Maryland, United States
- Cedar Clinical Research, Inc — Draper, Utah, United States
- La Nua Mental Health Centre — Galway, Ireland
- Cambridgeshire and Peterborough NHS Foundation Trust — Cambridge, England, United Kingdom
- Mirabilis Health — Belfast, Northern Ireland, United Kingdom
- NHS Greater Glasgow and Clyde — Glasgow, Scotland, United Kingdom
- Clerkenwell Health — London, United Kingdom
- Kings College — London, United Kingdom
Full record on ClinicalTrials.gov
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