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NCT02436239 · ClinicalTrials.gov registry record · Phase 3

A Study of Vilazodone in Pediatric Patients With Major Depressive Disorder

A Phase 3 study, sponsored by Forest Laboratories.

Completed
Registry status
Phase 3
Development phase
330
Enrollment target

NCT02436239: Completed Phase 3 study, sponsored by Forest Laboratories.

NCT02436239 is a Phase 3 study that has completed, run by Forest Laboratories. The registered enrollment target is 330 participants, below the 772-participant average among 15,282 other Phase 3 trials with a reported enrollment target (57% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT02436239, a Phase 3 study, has completed, sponsored by Forest Laboratories.

COMPLETED
Registry status
Phase 3
Development phase
330 participants
Enrollment target

Study Summary

The purpose of this study is to evaluate the long-term safety and tolerability of vilazodone for the treatment of MDD in pediatric outpatients (7-17 years).

Primary Outcome

The number of Participants who experienced a treatment emergent adverse events during the 27 week period from screening to the end of the open-label treatment period

Interventions

  • DRUG Vilazodone

Trial Details

FieldValue
Enrollment Target 330 participants
Start Date 2015-05-02
Est. Completion 2018-07-23
Phase Phase 3
Forest Laboratories

145 total trials

What the finished NCT02436239 record still lists

NCT02436239 is an interventional study that assigns participants to a tested intervention. The registered 330 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 (57% lower).

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

NCT02436239 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT02436239 about?

NCT02436239 is a clinical study titled "A Study of Vilazodone in Pediatric Patients With Major Depressive Disorder". The purpose of this study is to evaluate the long-term safety and tolerability of vilazodone for the treatment of MDD in pediatric outpatients (7-17 years).

What is the current status of trial NCT02436239?

This trial is currently completed. It is a Phase 3 study. The enrollment target is 330 participants. The study started on 2015-05-02. Estimated completion is 2018-07-23.

What interventions are being tested in trial NCT02436239?

The interventions under investigation include: Vilazodone (DRUG).

Who is sponsoring clinical trial NCT02436239?

This trial is sponsored by Forest Laboratories, which has 145 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT02436239's enrollment target sits among peer trials

330 1066th of 2000 higher than 927 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 NCT02436239, the US trial registry maintained by the National Library of Medicine. NCT02436239 (mid enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.