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NCT02970292 · ClinicalTrials.gov registry record · Phase 3
Efficacy and Safety of Adjunctive Pimavanserin for the Treatment of Schizophrenia (ENHANCE-1)
A Phase 3 study of Schizophrenia, sponsored by ACADIA Pharmaceuticals.
- Completed
- Registry status
- Phase 3
- Development phase
- 396
- Enrollment target
- 20
- Study locations
NCT02970292 is a Phase 3 study of Schizophrenia that has completed, run by ACADIA Pharmaceuticals. The registered enrollment target is 396 participants, above the 218-participant average among 315 other Schizophrenia trials with a reported enrollment target (82% higher). The trial reports 20 study locations across 6 states.
The verdict
NCT02970292, a Phase 3 study of Schizophrenia, has completed, sponsored by ACADIA Pharmaceuticals.
- COMPLETED
- Registry status
- Phase 3
- Development phase
- 396 participants
- Enrollment target
- 20
- Study locations
Study Summary
To evaluate the efficacy and safety of adjunctive pimavanserin compared with adjunctive placebo in the treatment of schizophrenia
Conditions Studied
Interventions
- DRUG Placebo
- DRUG Pimavanserin
Study Locations (20)
California
- - Bellflower
- - Cerritos
- - Culver City
- - Lemon Grove
- - Long Beach
- - San Diego
- - San Diego
- - Santa Ana
- - Torrance
Florida
- - Boca Raton
- - Lauderhill
- - Miami
Illinois
- - Chicago
- - Chicago
- - Hoffman Estates
Arkansas
- - Little Rock
- - Rogers
Georgia
- - Atlanta
- - Atlanta
Arizona
- - Phoenix
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 396 participants |
| Start Date | 2016-10-26 |
| Est. Completion | 2019-06-25 |
| Phase | Phase 3 |
Interested in This Trial?
Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT02970292
The ClinicalTrials.gov registry entry for NCT02970292 describes a study currently listed as completed, categorized as Phase 3. The registered enrollment target is 396 participants, a figure that helps gauge the scale of data the investigators plan to collect, above the 218-participant average among 315 other Schizophrenia trials with a reported enrollment target (82% higher). The listed sponsor is ACADIA Pharmaceuticals, which has 35 total studies on file at ClinicalTrials.gov.
The record links to 1 condition, with Schizophrenia appearing as the primary indexed condition, and to 2 interventions - of which Placebo is the first listed.
NCT02970292 reports 20 study locations spanning 6 distinct geographic areas - top geographies include California, Florida, Illinois.
Frequently Asked Questions
What is clinical trial NCT02970292 about?
NCT02970292 is a clinical study titled "Efficacy and Safety of Adjunctive Pimavanserin for the Treatment of Schizophrenia (ENHANCE-1)". To evaluate the efficacy and safety of adjunctive pimavanserin compared with adjunctive placebo in the treatment of schizophrenia
What is the current status of trial NCT02970292?
This trial is currently completed. It is a Phase 3 study. The enrollment target is 396 participants. The study started on 2016-10-26. Estimated completion is 2019-06-25.
What conditions does trial NCT02970292 study?
This clinical trial studies the following conditions: Schizophrenia.
What interventions are being tested in trial NCT02970292?
The interventions under investigation include: Placebo (DRUG), Pimavanserin (DRUG).
Who is sponsoring clinical trial NCT02970292?
This trial is sponsored by ACADIA Pharmaceuticals, which has 35 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT02970292 being conducted?
This trial has 20 study locations across Arizona, Arkansas, California, Florida, Georgia. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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Read our methodology - how this data is sourced, computed, and verified.
Related
Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.