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Completed Phase 3 Interventional Results available

Randomized, Double-blind, Placebo Controlled, Multi-center and Tolerability of RBP-7000 in Schizophrenia Patients

ClinicalTrials.gov ID: NCT02109562

Public ClinicalTrials.gov record NCT02109562. 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 23, 2026, 1:48 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 3, Randomized, Double-Blind, Placebo-Controlled, Multicenter Study to Evaluate the Efficacy, Safety and Tolerability of RBP-7000 as a Treatment in Subjects With Acute Schizophrenia Over 8 Weeks (2 Subcutaneous Doses)

Brief summary

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

The purpose of this study is to evaluate the efficacy and safety of RBP-7000 compared with placebo in the treatment of patients with schizophrenia. This will be a double-blind, placebo-controlled, Phase III study with 90 mg and 120 mg doses of RBP-7000 compared with placebo over an 8-week treatment period.

Study identification

NCT ID
NCT02109562
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Indivior Inc.
Industry
Enrollment
354 participants

Conditions and interventions

Conditions

Interventions

Drug

Eligibility (public fields only)

Age range
18 Years to 55 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
Apr 2014 (Type not available)
Primary completion
Nov 2014 (Actual)
Completion
Nov 2014 (Actual)
Last update posted
Oct 26, 2018

2014

United States locations

U.S. sites
32
U.S. states
15
U.S. cities
28
Facility City State ZIP Site status
Woodland International Research Group, Inc. Little Rock Arkansas 72211 —
Woodland International Research Group, Inc. Springdale Arkansas 72764 —
Comprehensive Clinical Development - Cerritos, CA Cerritos California 90703 —
Synergy Clinical Research of Escondido Escondido California 92025 —
Behavioral Research Specialists, LLC Glendale California 91206 —
Collaborative Neuroscience Networks, Inc. Long Beach California 90806 —
Apostle Clinical Trials, Inc. Long Beach California 90813 —
Pacific Research Partners Oakland California 94612 —
Excell Research, Inc. Oceanside California 92056 —
CNRI- Los Angeles, LLC Pico Rivera California 90660 —
CNRI - San Diego, LLC San Diego California 92012 —
Innovative Clinical Research Fort Lauderdale Florida 33308 —
Behavioral Clinical Research, Inc. North Miami Florida 33021 —
Florida Clinical Research Center, LLC Orlando Florida 32751 —
Uptown Research Institute Chicago Illinois 60640 —
Alexian Brothers Behavioral Health Hospital Hoffman Estates Illinois 60169 —
Via Christi Research Wichita Kansas 67214 —
Lake Charles Clinical Trials, LLC Lake Charles Louisiana 70629 —
J. Gary Booker, MD, APMC Shreveport Louisiana 71104-2136 —
St. Louis Clinical Trials St Louis Missouri 63118 —
PsychCare Consultants Research St Louis Missouri 63128 —
Altea Research Institute Las Vegas Nevada 89102 —
CRI Lifetree Marlton New Jersey 08053 —
Neurobehavioral Research, Inc. Cedarhurst New York 11516 —
New Hope Clinical Research Charlotte North Carolina 28204 —
Midwest Clinical Research Center, LLC Dayton Ohio 45417 —
Oklahoma Clinical Research Center Oklahoma City Oklahoma 73112 —
CRI Lifetree Philadelphia Pennsylvania 19139 —
FutureSearch Clinical Trials, L.P. Austin Texas 78734 —
Community Clinical Research, Inc. Austin Texas 78754 —
FutureSearch Clinical Trials, L.P. Dallas Texas 75231 —
Pillar Clinic Research, LLC Dallas Texas 75243 —

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 NCT02109562, 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 Oct 26, 2018 · Synced Oct 23, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT02109562 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →