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Terminated Phase 3 Interventional Results available

Brexpiprazole as an Adjunctive Treatment to Paroxetine or Sertraline in Adult Patients Suffering From Post-traumatic Stress Disorder (PTSD)

ClinicalTrials.gov ID: NCT01987960

Public ClinicalTrials.gov record NCT01987960. 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 May 7, 2026, 9:03 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

Interventional, Randomised, Double-blind, Parallel-group, Placebo-controlled, Flexible-dose Study of Brexpiprazole as Adjunctive Treatment to Paroxetine or Sertraline in Adult Patients Suffering From Post-traumatic Stress Disorder (PTSD)

Study identification

NCT ID
NCT01987960
Recruitment status
Terminated
Study type
Interventional
Phase
Phase 3
Lead sponsor
H. Lundbeck A/S
Industry
Enrollment
417 participants

Conditions and interventions

Interventions

  • Brexpiprazole Drug
  • Placebo Drug

Drug

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
Nov 30, 2013
Primary completion
Sep 30, 2015
Completion
Sep 30, 2015
Last update posted
Mar 12, 2017

2013 – 2015

United States locations

U.S. sites
22
U.S. states
13
U.S. cities
20
Facility City State ZIP Site status
US004 Los Angeles California 90024
US025 Los Angeles California 90102
US024 Riverside California 92504
US015 San Diego California 90103
US008 San Diego California 92123
US002 Bradenton Florida 34201
US006 Gainesville Florida 32607
US016 Jacksonville Florida 32256
US020 North Miami Florida 33161
US017 Tampa Florida 33609
US012 Indianapolis Indiana 46260
US021 Roslindale Massachusetts 02131
US019 Las Vegas Nevada 89102
US007 Nashua New Hampshire 03060
US001 The Bronx New York 10467
US009 Cincinnati Ohio 45219
US005 Dayton Ohio 45417
US010 Portland Oregon 97210
US014 Norristown Pennsylvania 19403
US011 Memphis Tennessee 38119
US003 Austin Texas 78731
US026 Seattle Washington 98104

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 37 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT01987960, 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 Mar 12, 2017 · Synced May 7, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT01987960 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →