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Terminated Phase 3 Interventional Results available

12-Week Open-Label Extension Study of TNX-102 SL in PTSD Patients

ClinicalTrials.gov ID: NCT03110575

Public ClinicalTrials.gov record NCT03110575. 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.

ClinicalTrials.gov public records Last synced Sep 2, 2026, 5:27 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A 12-Week Open-Label Extension Study to Evaluate TNX-102 SL Taken Daily at Bedtime in Patients With PTSD

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

This is an open-label, extension trial designed to evaluate safety over 12 additional weeks of TNX-102 SL therapy taken daily at bedtime for the treatment of PTSD. Patients recruited into this trial are those who have successfully completed the double-blind lead-in study.

Study identification

NCT ID
NCT03110575
Recruitment status
Terminated
Study type
Interventional
Phase
Phase 3
Lead sponsor
Tonix Pharmaceuticals, Inc.
Industry
Enrollment
190 participants

Conditions and interventions

Conditions

Interventions

Drug

Eligibility (public fields only)

Age range
18 Years to 75 Years
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
Jun 19, 2017
Primary completion
Jul 26, 2018
Completion
Jul 26, 2018
Last update posted
Feb 5, 2025

2017 – 2018

United States locations

U.S. sites
32
U.S. states
15
U.S. cities
31
Facility City State ZIP Site status
Phoenix Phoenix Arizona 85032
Rogers Rogers Arkansas 72758
Beverly Hills Beverly Hills California 90210
Glendale Glendale California 91206
Oakland Oakland California 94607
Oceanside Oceanside California 92056
Orange Orange California 92868
Riverside Riverside California 92506
San Diego San Diego California 92123
San Diego San Diego California 92161
Temecula Temecula California 92591
Colorado Springs Colorado Springs Colorado 80910
Jacksonville Jacksonville Florida 32256
Lake City Lake City Florida 32607
Lauderhill Lauderhill Florida 33319
Tampa Tampa Florida 33609
Atlanta Atlanta Georgia 30341
New Bedford New Bedford Massachusetts 02740
Flowood Flowood Mississippi 39232
Las Vegas Las Vegas Nevada 89102
Berlin Berlin New Jersey 08009
Cedarhurst Cedarhurst New York 11516
New York New York New York 10128
Canton Canton Ohio 44718
Cincinnati Cincinnati Ohio 45219
Dayton Dayton Ohio 45417
Oklahoma City Oklahoma City Oklahoma 73103
Charleston Charleston South Carolina 29407
Austin Austin Texas 78754
Dallas Dallas Texas 75231
Houston Houston Texas 77098
San Antonio San Antonio Texas 78229

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 NCT03110575, 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 Feb 5, 2025 · Synced Sep 2, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT03110575 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →