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NCT03668600 · ClinicalTrials.gov registry record · Phase 3

Study of Adjunctive or Monotherapy Rapastinel Treatment in Patients With Major Depressive Disorder (MDD)

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

Terminated
Registry status
Phase 3
Development phase
230
Enrollment target

NCT03668600: Clinical Trial Phase 3 study, sponsored by Naurex, Inc, an affiliate of Allergan.

NCT03668600 is a Phase 3 study that was terminated before completion, run by Naurex, Inc, an affiliate of Allergan. The registered enrollment target is 230 participants, below the 772-participant average among 15,282 other Phase 3 trials with a reported enrollment target (70% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT03668600, a Phase 3 study, was terminated before completion, sponsored by Naurex, Inc, an affiliate of Allergan.

TERMINATED
Registry status
Phase 3
Development phase
230 participants
Enrollment target

Study Summary

Multicenter, open-label, long-term extended access treatment protocol in adult patients with a primary diagnosis of MDD.

Primary Outcome

A Treatment Emergent Adverse Event was considered any unfavorable and unintended sign, symptom, or disease associated with the use of the study drug, whether or not considered related to the study drug. An Adverse Drug Reaction was a harmful and unintended reaction that is incurred during routine administration or use of the drug, whose causal relationship with the drug cannot be excluded.

Interventions

  • DRUG Rapastinel

Trial Details

FieldValue
Enrollment Target 230 participants
Start Date 2018-08-23
Est. Completion 2019-07-03
Phase Phase 3

Why NCT03668600 stopped before completion

NCT03668600 is an interventional study that assigns participants to a tested intervention. The registered 230 participants enrollment target is mid-sized for trials with a published cap, below the 772-participant average among 15,282 other Phase 3 trials with a reported enrollment target (70% lower).

The record links to 0 conditions, and to 1 intervention - of which Rapastinel is the first listed.

NCT03668600 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT03668600 about?

NCT03668600 is a clinical study titled "Study of Adjunctive or Monotherapy Rapastinel Treatment in Patients With Major Depressive Disorder (MDD)". Multicenter, open-label, long-term extended access treatment protocol in adult patients with a primary diagnosis of MDD.

What is the current status of trial NCT03668600?

This trial is currently terminated. It is a Phase 3 study. The enrollment target is 230 participants. The study started on 2018-08-23. Estimated completion is 2019-07-03.

What interventions are being tested in trial NCT03668600?

The interventions under investigation include: Rapastinel (DRUG).

Who is sponsoring clinical trial NCT03668600?

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

How this trial's enrollment target compares

Where NCT03668600's enrollment target sits among peer trials

230 1304th of 2000 higher than 692 of 2,000 other Phase 3 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 3 trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT03668600, the US trial registry maintained by the National Library of Medicine. NCT03668600 (mid enrollment · none site footprint · terminated) retrieved and formatted by PlainTrial, see methodology.