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Completed Phase 2 Interventional

A Study of RO4917838 (Bitopertin) in Patients With Acute Exacerbation of Schizophrenia

ClinicalTrials.gov ID: NCT01234779

Public ClinicalTrials.gov record NCT01234779. 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 Jun 25, 2026, 4:54 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 II, Multi-center, Randomized, 4-week, Double-blind, Parallel Group, Placebo and Active-controlled Trial of the Safety and Efficacy of RO4917838 vs. Placebo in Patients With an Acute Exacerbation of Schizophrenia

Study identification

NCT ID
NCT01234779
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Hoffmann-La Roche
Industry
Enrollment
301 participants

Conditions and interventions

Conditions

Interventions

  • bitopertin [RO4917838] Drug
  • olanzapine 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
Jan 31, 2011
Primary completion
Aug 31, 2012
Completion
Aug 31, 2012
Last update posted
Nov 1, 2016

2011 – 2012

United States locations

U.S. sites
19
U.S. states
13
U.S. cities
19
Facility City State ZIP Site status
Not listed Little Rock Arkansas 72201
Not listed Cerritos California 90703
Not listed Oceanside California 92056
Not listed Pico Rivera California 90660
Not listed San Diego California 92121
Not listed Lauderhill Florida 33021
Not listed North Miami Florida 33161
Not listed Atlanta Georgia 30308
Not listed Lake Charles Louisiana 70601
Not listed Flowood Mississippi 39232
Not listed St Louis Missouri 63141
Not listed Willingboro New Jersey 08046
Not listed Holliswood New York 11423
Not listed New York New York 11004
Not listed Cincinnati Ohio 45219
Not listed Philadelphia Pennsylvania 19139
Not listed Charlesston South Carolina 29405
Not listed Austin Texas 78754
Not listed Irving Texas 75062

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 27 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT01234779, 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 1, 2016 · Synced Jun 25, 2026

Related: full search, browse by condition, browse by drug or therapy, browse by sponsor, browse by U.S. city.

Open the official record

The complete protocol, eligibility criteria, and contact information for NCT01234779 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →