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NCT02951988 · ClinicalTrials.gov registry record · Phase 3

A Study of Rapastinel as Adjunctive Therapy in the Prevention of Relapse in Patients With Major Depressive Disorder

A Phase 3 study, sponsored by Naurex, Inc, an affiliate of Allergan.

Completed
Registry status
Phase 3
Development phase
1,304
Enrollment target

NCT02951988 is a Phase 3 study that has completed, run by Naurex, Inc, an affiliate of Allergan. The registered enrollment target is 1,304 participants.

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The verdict

NCT02951988, a Phase 3 study, has completed, sponsored by Naurex, Inc, an affiliate of Allergan.

COMPLETED
Registry status
Phase 3
Development phase
1,304 participants
Enrollment target

Study Summary

This study will evaluate the efficacy, safety and tolerability of rapastinel 450 milligrams (mg) intravenous (IV) once weekly or once every 2 weeks versus placebo as an adjunctive treatment to ongoing anti-depressive therapy (ADT) in the prevention of relapse in participants with Major Depressive Disorder (MDD).

Interventions

  • DRUG Rapastinel
  • DRUG Placebo-matching Rapastinel

Trial Details

FieldValue
Enrollment Target 1,304 participants
Start Date 2016-11-13
Est. Completion 2019-02-22
Phase Phase 3

What the Registry Record Tells You About NCT02951988

The ClinicalTrials.gov registry entry for NCT02951988 describes a study currently listed as completed, categorized as Phase 3. The registered enrollment target is 1,304 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Naurex, Inc, an affiliate of Allergan, which has 18 total studies on file at ClinicalTrials.gov.

The record links to 0 conditions, and to 2 interventions - of which Rapastinel is the first listed.

NCT02951988 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT02951988 about?

NCT02951988 is a clinical study titled "A Study of Rapastinel as Adjunctive Therapy in the Prevention of Relapse in Patients With Major Depressive Disorder". This study will evaluate the efficacy, safety and tolerability of rapastinel 450 milligrams (mg) intravenous (IV) once weekly or once every 2 weeks versus placebo as an adjunctive treatment to ongoing anti-depressive therapy (ADT) in the prevention of relapse in participants with Major Depressive Di...

What is the current status of trial NCT02951988?

This trial is currently completed. It is a Phase 3 study. The enrollment target is 1,304 participants. The study started on 2016-11-13. Estimated completion is 2019-02-22.

What interventions are being tested in trial NCT02951988?

The interventions under investigation include: Rapastinel (DRUG), Placebo-matching Rapastinel (DRUG).

Who is sponsoring clinical trial NCT02951988?

This trial is sponsored by Naurex, Inc, an affiliate of Allergan, which has 18 total clinical trials registered on ClinicalTrials.gov.

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

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.