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Terminated Phase 2 Interventional

A Clinical Trial of PRAX-114 in Participants With Post-Traumatic Stress Disorder

ClinicalTrials.gov ID: NCT05260541

Public ClinicalTrials.gov record NCT05260541. 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 11, 2026, 5:06 PM 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 Phase 2, Randomized, Placebo-Controlled Trial to Evaluate the Efficacy and Safety of PRAX-114 in Participants With Post-Traumatic Stress Disorder

Brief summary

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

This trial is comprised of a 4-week randomized, double-blind, placebo-controlled treatment period followed by an optional 8-week open-label extension (OLE) period. This trial will evaluate the efficacy and safety of oral PRAX-114 flexibly dosed at 40 to 60 mg for 4 weeks compared to placebo in adults with PTSD. The OLE period consisting of treatment with 40 mg PRAX-114 for 8 weeks will provide additional efficacy and safety data.

Study identification

NCT ID
NCT05260541
Recruitment status
Terminated
Study type
Interventional
Phase
Phase 2
Lead sponsor
Praxis Precision Medicines
Industry
Enrollment
11 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years to 65 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
Jan 24, 2022
Primary completion
Jul 31, 2022
Completion
Sep 22, 2022
Last update posted
Nov 30, 2022

2022

United States locations

U.S. sites
17
U.S. states
12
U.S. cities
17
Facility City State ZIP Site status
Praxis Research Site Phoenix Arizona 85012
Praxis Research Site Little Rock Arkansas 72211
Praxis Research Site Rogers Arkansas 72758
Praxis Research Site Lemon Grove California 91945
Praxis Research Site Westlake Village California 91362
Praxis Research Site Fort Myers Florida 33908
Praxis Research Site Decatur Georgia 30030
Praxis Research Site Boston Massachusetts 02131
Praxis Research Site Las Vegas Nevada 89102
Praxis Research Site Cincinnati Ohio 45219
Praxis Research Site Dayton Ohio 45417
Praxis Research Site Oklahoma City Oklahoma 73118
Praxis Research Site Allentown Pennsylvania 18104
Praxis Research Site Media Pennsylvania 19063
Praxis Research Site Austin Texas 78737
Praxis Research Site Dallas Texas 75231
Praxis Research Site Everett Washington 98201

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 NCT05260541, 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 Nov 30, 2022 · Synced Sep 11, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT05260541 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →