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NCT02102698 · ClinicalTrials.gov registry record · Phase 2

Ecopipam Treatment of Tourette's Syndrome in Subjects 7-17 Years

A Phase 2 study, sponsored by Emalex Biosciences.

Completed
Registry status
Phase 2
Development phase
40
Enrollment target

NCT02102698: Completed Phase 2 study, sponsored by Emalex Biosciences.

NCT02102698 is a Phase 2 study that has completed, run by Emalex Biosciences. The registered enrollment target is 40 participants, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (70% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT02102698, a Phase 2 study, has completed, sponsored by Emalex Biosciences.

COMPLETED
Registry status
Phase 2
Development phase
40 participants
Enrollment target

Study Summary

Tourette's Syndrome is a neurological disease characterized by motor and vocal tics. It has been hypothesized that abnormal interactions of dopamine with its receptors may cause the tics. The purpose of this study is to test the hypothesis that a drug (ecopipam) that selectively blocks dopamine D1/D5 receptors can reduce the frequency and severity of the tics.

Primary Outcome

The Yale Global Tic Severity Scale (YGTSS) is the standard rating scale used to assess the effects of a new treatment on the symptoms of Tourette's Disorder (TD). The YGTSS is a clinician-rated, multi-dimensional instrument for assessing tic symptom severity in children and adults with TD. Both motor and vocal tics are assessed for symptom number, frequency, intensity, complexity, and interference on a 0-5 Likert scale. Scores from each dimension are totaled to reflect the severity of motor tic

Interventions

  • DRUG Ecopipam

Trial Details

FieldValue
Enrollment Target 40 participants
Start Date 2014-06-19
Est. Completion 2019-12
Phase Phase 2
Emalex Biosciences

14 total trials

What the finished NCT02102698 record still lists

NCT02102698 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 40 participants, a relatively small participant target, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (70% lower).

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

NCT02102698 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT02102698 about?

NCT02102698 is a clinical study titled "Ecopipam Treatment of Tourette's Syndrome in Subjects 7-17 Years". Tourette's Syndrome is a neurological disease characterized by motor and vocal tics. It has been hypothesized that abnormal interactions of dopamine with its receptors may cause the tics. The purpose of this study is to test the hypothesis that a drug (ecopipam) that selectively blocks dopamine D1/D...

What is the current status of trial NCT02102698?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 40 participants. The study started on 2014-06-19. Estimated completion is 2019-12.

What interventions are being tested in trial NCT02102698?

The interventions under investigation include: Ecopipam (DRUG).

Who is sponsoring clinical trial NCT02102698?

This trial is sponsored by Emalex Biosciences, which has 14 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT02102698's enrollment target sits among peer trials

40 1362nd of 2000 higher than 542 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 NCT02102698, the US trial registry maintained by the National Library of Medicine. NCT02102698 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.