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NCT02192099 · ClinicalTrials.gov registry record · Phase 2

Open Label Extension for GLYX13-C-202, NCT01684163

A Phase 2 study, sponsored by Naurex, Inc, an affiliate of Allergan.

Terminated
Registry status
Phase 2
Development phase
61
Enrollment target

NCT02192099: Clinical Trial Phase 2 study, sponsored by Naurex, Inc, an affiliate of Allergan.

NCT02192099 is a Phase 2 study that was terminated before completion, run by Naurex, Inc, an affiliate of Allergan. The registered enrollment target is 61 participants, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (54% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT02192099, a Phase 2 study, was terminated before completion, sponsored by Naurex, Inc, an affiliate of Allergan.

TERMINATED
Registry status
Phase 2
Development phase
61 participants
Enrollment target

Study Summary

Examine the safety of long term repeat exposure to GLYX-13 in subjects who participated in GLYX13-C-202.

Primary Outcome

An adverse event (AE) was any untoward medical occurrence in a patient or clinical investigation participant administered a pharmaceutical product and that does not necessarily have a causal relationship with this treatment. A TEAE was an AE that occurred after receiving the first dose of investigational product or an AE present prior to first dose but increased in severity during the Treatment Period.

Interventions

  • DRUG Rapastinel (225 mg/450 mg IV administration)

Trial Details

FieldValue
Enrollment Target 61 participants
Start Date 2014-09-08
Est. Completion 2018-11-08
Phase Phase 2

Why NCT02192099 stopped before completion

NCT02192099 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 61 participants, a relatively small participant target, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (54% lower).

The record links to 0 conditions, and to 1 intervention - of which Rapastinel (225 mg/450 mg IV administration) is the first listed.

NCT02192099 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT02192099 about?

NCT02192099 is a clinical study titled "Open Label Extension for GLYX13-C-202, NCT01684163". Examine the safety of long term repeat exposure to GLYX-13 in subjects who participated in GLYX13-C-202.

What is the current status of trial NCT02192099?

This trial is currently terminated. It is a Phase 2 study. The enrollment target is 61 participants. The study started on 2014-09-08. Estimated completion is 2018-11-08.

What interventions are being tested in trial NCT02192099?

The interventions under investigation include: Rapastinel (225 mg/450 mg IV administration) (DRUG).

Who is sponsoring clinical trial NCT02192099?

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 NCT02192099's enrollment target sits among peer trials

61 1026th of 2000 higher than 974 of 2,000 other Phase 2 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 2 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 NCT02192099, the US trial registry maintained by the National Library of Medicine. NCT02192099 (small enrollment · none site footprint · terminated) retrieved and formatted by PlainTrial, see methodology.