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NCT01234779 · ClinicalTrials.gov registry record · Phase 2

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

A Phase 2 study, sponsored by Hoffmann-La Roche.

Completed
Registry status
Phase 2
Development phase
301
Enrollment target

NCT01234779 is a Phase 2 study that has completed, run by Hoffmann-La Roche. The registered enrollment target is 301 participants.

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The verdict

NCT01234779, a Phase 2 study, has completed, sponsored by Hoffmann-La Roche.

COMPLETED
Registry status
Phase 2
Development phase
301 participants
Enrollment target

Study Summary

This randomized, double-blind, placebo- and active-controlled, parallel group study will evaluate the safety and efficacy of RO4917838 (bitopertin) in patients with acute exacerbation of schizophrenia. Patients will be randomized to receive either RO4917838 10 mg or RO4917838 30 mg or olanzapine 15 mg or placebo orally daily for 4 weeks as inpatients, with a 4-week follow-up period.

Interventions

  • DRUG placebo
  • DRUG olanzapine
  • DRUG bitopertin [RO4917838]

Trial Details

FieldValue
Enrollment Target 301 participants
Start Date 2011-02
Est. Completion 2012-09
Phase Phase 2

Sponsor

Hoffmann-La Roche

909 total trials

What the Registry Record Tells You About NCT01234779

The ClinicalTrials.gov registry entry for NCT01234779 describes a study currently listed as completed, categorized as Phase 2. The registered enrollment target is 301 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Hoffmann-La Roche, which has 909 total studies on file at ClinicalTrials.gov.

The record links to 0 conditions, and to 3 interventions - of which placebo is the first listed.

NCT01234779 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT01234779 about?

NCT01234779 is a clinical study titled "A Study of RO4917838 (Bitopertin) in Patients With Acute Exacerbation of Schizophrenia". This randomized, double-blind, placebo- and active-controlled, parallel group study will evaluate the safety and efficacy of RO4917838 (bitopertin) in patients with acute exacerbation of schizophrenia. Patients will be randomized to receive either RO4917838 10 mg or RO4917838 30 mg or olanzapine 15 ...

What is the current status of trial NCT01234779?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 301 participants. The study started on 2011-02. Estimated completion is 2012-09.

What interventions are being tested in trial NCT01234779?

The interventions under investigation include: placebo (DRUG), olanzapine (DRUG), bitopertin [RO4917838] (DRUG).

Who is sponsoring clinical trial NCT01234779?

This trial is sponsored by Hoffmann-La Roche, which has 909 total clinical trials registered on ClinicalTrials.gov.

Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.