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NCT02195700 · ClinicalTrials.gov registry record · Phase 2

Aim to Reduce Movements in Tardive Dyskinesia

A Phase 2 study, sponsored by Auspex Pharmaceuticals.

Completed
Registry status
Phase 2
Development phase
117
Enrollment target

NCT02195700: Completed Phase 2 study, sponsored by Auspex Pharmaceuticals.

NCT02195700 is a Phase 2 study that has completed, run by Auspex Pharmaceuticals. The registered enrollment target is 117 participants, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (12% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT02195700, a Phase 2 study, has completed, sponsored by Auspex Pharmaceuticals.

COMPLETED
Registry status
Phase 2
Development phase
117 participants
Enrollment target

Study Summary

The purpose of this study is to determine whether an investigational drug, SD-809 (deutetrabenazine), will reduce the severity of abnormal involuntary movements of tardive dyskinesia.

Primary Outcome

AIMS is an assessment tool used to detect and follow the severity of TD over time. The AIMS is composed of 12 clinician-administered and scored items. AIMS was digitally video recorded using a standard protocol and independently reviewed by blinded central raters who were experts in movement disorders. This outcome sums items 1 through 7 which cover orofacial movements, and extremity and truncal dyskinesia. Severity ratings were from 0 (none) to 4 (severe) for a total scale of 0 (no orofacial,

Interventions

  • DRUG Placebo
  • DRUG SD-809

Trial Details

FieldValue
Enrollment Target 117 participants
Start Date 2014-06
Est. Completion 2015-05
Phase Phase 2
Auspex Pharmaceuticals

5 total trials

What the finished NCT02195700 record still lists

NCT02195700 is an interventional study that assigns participants to a tested intervention. The registered 117 participants enrollment target is mid-sized for trials with a published cap, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (12% lower).

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

NCT02195700 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT02195700 about?

NCT02195700 is a clinical study titled "Aim to Reduce Movements in Tardive Dyskinesia". The purpose of this study is to determine whether an investigational drug, SD-809 (deutetrabenazine), will reduce the severity of abnormal involuntary movements of tardive dyskinesia.

What is the current status of trial NCT02195700?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 117 participants. The study started on 2014-06. Estimated completion is 2015-05.

What interventions are being tested in trial NCT02195700?

The interventions under investigation include: Placebo (DRUG), SD-809 (DRUG).

Who is sponsoring clinical trial NCT02195700?

This trial is sponsored by Auspex Pharmaceuticals, which has 5 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT02195700's enrollment target sits among peer trials

117 623rd of 2000 higher than 1,378 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 NCT02195700, the US trial registry maintained by the National Library of Medicine. NCT02195700 (mid enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.