An Evaluation of the Safety and Efficacy of TSND-201 for the Treatment of PTSD (EMPOWER-1)
Public ClinicalTrials.gov record NCT07456696. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.
Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.
Official title
A Phase 3, Randomized, Double-Blind, Placebo-Controlled, Evaluation of the Safety and Efficacy of TSND-201 for the Treatment of PTSD
Study identification
- NCT ID
- NCT07456696
- Recruitment status
- Recruiting
- Study type
- Interventional
- Phase
- Phase 3
- Lead sponsor
- Transcend Therapeutics
- Industry
- Enrollment
- 300 participants
Conditions and interventions
Conditions
Interventions
- Placebo Drug
- TSND-201 Drug
Drug
Eligibility (public fields only)
- Age range
- 18 Years and older
- Sex
- All
- Healthy volunteers
- Healthy volunteers not accepted
This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.
Study timeline
- Start date
- Apr 1, 2026
- Primary completion
- Nov 30, 2027
- Completion
- Nov 30, 2027
- Last update posted
- May 4, 2026
2026 – 2027
United States locations
- U.S. sites
- 19
- U.S. states
- 12
- U.S. cities
- 19
| Facility | City | State | ZIP | Site status |
|---|---|---|---|---|
| Preferred Research Partners | Little Rock | Arkansas | 72211 | Recruiting |
| CalNeuro Research Group | Los Angeles | California | 90025 | Recruiting |
| Catalina Research Institute | Montclair | California | 91763 | Recruiting |
| Inland Psychiatric Medical Group | San Juan Capistrano | California | 92675 | Recruiting |
| Starlight Clinical Research | Evergreen | Colorado | 80439 | Recruiting |
| CNS Healthcare | Jacksonville | Florida | 32256 | Recruiting |
| Segal Trials | Lauderhill | Florida | 33319 | Recruiting |
| Accel Clinical Research | Maitland | Florida | 32751 | Recruiting |
| CNS Healthcare | Orlando | Florida | 32801 | Recruiting |
| Uptown Research Institute | Chicago | Illinois | 60640 | Recruiting |
| Vitalix Clinical | Worcester | Massachusetts | 01608 | Recruiting |
| Midwest Research GRoup | Saint Charles | Missouri | 63304 | Recruiting |
| Global Medical Institutes | Princeton | New Jersey | 08540 | Recruiting |
| Bio Behavioral Health | Toms River | New Jersey | 08755 | Recruiting |
| Insight Clinical Trials | Independence | Ohio | 44131 | Recruiting |
| Suburban Research Associates | West Chester | Pennsylvania | 19380 | Recruiting |
| Austin Clinical Trial Partners | Austin | Texas | 78737 | Recruiting |
| Haracec Clinical Research | El Paso | Texas | 79902 | Recruiting |
| Inner Space Research | Orem | Utah | 84058 | Recruiting |
Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.
About this trial record page
- What this page shows
- Public field values for ClinicalTrials.gov record NCT07456696, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
- What this page does not do
- No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
- Where the data comes from
- Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
- Last refresh
- Last update posted May 4, 2026 · Synced May 6, 2026
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Open the official record
The complete protocol, eligibility criteria, and contact information for NCT07456696 live on ClinicalTrials.gov.