Independent directory Public ClinicalTrials.gov records United States
ClinicalTrials.gov record
Completed Phase 2 Interventional

A Study of Bitopertin (RO4917838) in Combination With Selective Serotonin Reuptake Inhibitors (SSRIs) in Participants With Obsessive-Compulsive Disorder (OCD)

ClinicalTrials.gov ID: NCT01674361

Public ClinicalTrials.gov record NCT01674361. 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 19, 2026, 5:10 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 II, Multicenter, Randomized, Double-Blind, Parallel-Group, Placebo-Controlled Study to Evaluate Efficacy and Safety of RO4917838 in Combination With Selective Serotonin Reuptake Inhibitors in Patients With Obsessive Compulsive Disorder

Brief summary

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

This multicenter, randomized, double-blind, parallel-group, placebo-controlled study will evaluate the efficacy and safety of bitopertin in combination with SSRI in participants with obsessive-compulsive disorder. Participants will be randomized to receive either bitopertin 30 milligrams (mg) or bitopertin 10 mg or placebo orally daily in addition to their background therapy with an SSRI. Participants will be allocated to one of two strata. Participants in Stratum 1 will start study drug on Day 1. Participants in Stratum 2 will receive placebo from Day 1 (placebo lead-in) and will then start study drug at the Week 2 visit. Participants in both strata will receive the study drug in addition to their background therapy with an SSRI until Week 16.

Study identification

NCT ID
NCT01674361
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Hoffmann-La Roche
Industry
Enrollment
99 participants

Conditions and interventions

Interventions

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
Dec 31, 2012 (Actual)
Primary completion
Apr 30, 2015 (Actual)
Completion
Apr 30, 2015 (Actual)
Last update posted
Aug 2, 2017

2012 – 2015

United States locations

U.S. sites
27
U.S. states
19
U.S. cities
25
Facility City State ZIP Site status
Excell Research Oceanside California 92056 —
Stanford University School of Medicine Stanford California 94305 —
Yale University School of Medicine; Neuroscience Research Training Program New Haven Connecticut 06519 —
Compass Research North, LLC Leesburg Florida 34748 —
Medical Research Group of Central Florida Orange City Florida 3273 —
University of South Florida St. Petersburg Florida 33701 —
University of South Florida Tampa Florida 33613-4706 —
iResearch Atlanta Decatur Georgia 30030 —
Carman Research Smyrna Georgia 30080 —
Uni of Chicago; Centre For Advanced Medicine Chicago Illinois 60637 —
Louisiana Research Associates New Orleans Louisiana 70114 —
Massachusetts General Hospital - East Boston Massachusetts 02114 —
Boston Clinical Trials Boston Massachusetts 02131 —
Ambulatory Research Center (ARC), Department of Psychiatry Minneapolis Minnesota 55454 —
Precise Research Centers Flowood Mississippi 39232 —
St Louis Clinical Trials St Louis Missouri 63141 —
Mount Sinai School of Medicine; Department of Psychiatry New York New York 10029 —
Medical Research Network - New York New York New York 10128 —
Finger Lakes Clinical Research Rochester New York 14618 —
North Star Research Middleburg Heights Ohio 44130 —
Ips Research Company Oklahoma City Oklahoma 73103 —
Keystone Clinical Studies, LLC Norristown Pennsylvania 19403 —
Butler Hospital - Department of Psychiatry and Human Behavior Providence Rhode Island 02906 —
Clinical Neuroscience Solutions,Inc Memphis Tennessee 38119 —
FutureSearch Trials, LP Austin Texas 78731 —
Eastside Therapeutic Resource Kirkland Washington 98033 —
Dean Foundation Middleton Wisconsin 53562 —

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 7 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT01674361, 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 Aug 2, 2017 · Synced Oct 19, 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 public registry record, listed eligibility criteria, and available contact information for NCT01674361 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →