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Completed Phase 2 Interventional Results available

A Study of Flexible Dose Brexpiprazole as Monotherapy or Combination Therapy in the Treatment of Adults With Post-traumatic Stress Disorder (PTSD)

ClinicalTrials.gov ID: NCT03033069

Public ClinicalTrials.gov record NCT03033069. 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 Oct 27, 2026, 11:30 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 Phase 2, Multicenter, Randomized, Double-blind, Placebo- and Active-controlled Trial of Brexpiprazole (1 - 3 mg/Day) as Monotherapy or as Combination Therapy in the Treatment of Adults With Post-traumatic Stress Disorder

Brief summary

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

To evaluate the safety, efficacy and tolerability of brexpiprazole (with placebo) as monotherapy or combination therapy with Zoloft (sertraline) in adults with PTSD.

Study identification

NCT ID
NCT03033069
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Enrollment
336 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 26, 2017 (Actual)
Primary completion
Nov 12, 2018 (Actual)
Completion
Nov 12, 2018 (Actual)
Last update posted
Dec 8, 2021

2017 – 2018

United States locations

U.S. sites
54
U.S. states
22
U.S. cities
51
Facility City State ZIP Site status
Investigational Site Tuscaloosa Alabama 35404 —
Investigational Site Phoenix Arizona 85032 —
Investigational Site Little Rock Arkansas 72211 —
Investigational Site Rogers Arkansas 72758 —
Investigational Site Bellflower California 90706 —
Investigational Site Beverly Hills California 90210 —
Investigational Site Glendale California 91206 —
Investigational Site National City California 91950 —
Investigational Site Oceanside California 92054 —
Investigational Site Oceanside California 92056 —
Investigational Site Orange California 92868 —
Investigational Site Redlands California 92374 —
Investigational Site Riverside California 92506 —
Investigational Site San Diego California 92103 —
Investigational Site San Marcos California 92078 —
Investigational Site Torrance California 90502 —
Investigational Site Colorado Springs Colorado 80910 —
Investigational Site Bradenton Florida 34201 —
Investigational Site Fort Lauderdale Florida 33319 —
Investigational Site Fort Myers Florida 33912 —
Investigational Site Gainesville Florida 32607 —
Investigational Site Jacksonville Florida 32256 —
Investigational Site North Miami Florida 33161 —
Investigational Site Orlando Florida 32801 —
Investigational Site Orlando Florida 32806 —
Investigational Site Tampa Florida 33614 —
Investigational Site Atlanta Georgia 30341 —
Investigational Site Decatur Georgia 30030 —
Investigational Site Roswell Georgia 30076 —
Investigational Site Chicago Illinois 60640 —
Investigational Site St Louis Missouri 63141 —
Investigational Site Las Vegas Nevada 89102 —
Investigational Site Berlin New Jersey 08009 —
Investigational Site Princeton New Jersey 08540 —
Investigational Site Brooklyn New York 11235 —
Investigational Site Cedarhurst New York 11516 —
Investigational Site New York New York 10128 —
Investigational Site Rochester New York 14618 —
Investigational Site Charlotte North Carolina 28211 —
Investigational Site Raleigh North Carolina 27609 —
Investigational Site Cincinnati Ohio 45215 —
Investigational Site Oklahoma City Oklahoma 73103 —
Investigational Site Oklahoma City Oklahoma 73118 —
Investigational Site Portland Oregon 97214 —
Investigational Site Salem Oregon 97301 —
Investigational Site Media Pennsylvania 19063 —
Investigational Site Norristown Pennsylvania 19403 —
Investigational Site Lincoln Rhode Island 02865 —
Investigational Site Charleston South Carolina 29401 —
Investigational Site Memphis Tennessee 38119 —
Investigational Site Bellaire Texas 77401 —
Investigational Site San Antonio Texas 78229 —
Investigational Site Wichita Falls Texas 76309 —
Investigational 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 NCT03033069, 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 Dec 8, 2021 · Synced Oct 27, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT03033069 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →