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Efficacy, Safety, and Tolerability of AVP-786 for the Treatment of Residual Schizophrenia
NCT02477670 · View on ClinicalTrials.gov ↗
Study Summary
The objectives of this 12-week study are to evaluate the efficacy, safety, and tolerability of AVP-786 as an adjunctive treatment compared with placebo in patients with residual schizophrenia.
Conditions Studied
Interventions
- DRUG Placebo
- DRUG AVP-786
Study Locations (17)
California
- — Cerritos
- — Garden Grove
- — National City
- — Oakland
- — San Diego
New York
- — Jamaica
- — New York
- — Rochester
Georgia
- — Atlanta
- — Augusta
Massachusetts
- — Boston
- — Worcester
District of Columbia
- — Washington D.C.
Florida
- — Orlando
Illinois
- — Chicago
Michigan
- — Grand Rapids
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 145 participants |
| Start Date | 2015-09 |
| Est. Completion | 2017-07-21 |
| Phase | Phase 2 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT02477670
The ClinicalTrials.gov registry entry for NCT02477670 describes a study currently listed as completed. It is categorized as Phase 2, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 145 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Avanir Pharmaceuticals, which has 4 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.
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. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.
Geographic footprint matters for practical reasons: NCT02477670 reports 17 study locations spanning 9 distinct geographic areas — top geographies include California, New York, Georgia. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.
Frequently Asked Questions
What is clinical trial NCT02477670 about?
NCT02477670 is a clinical study titled "Efficacy, Safety, and Tolerability of AVP-786 for the Treatment of Residual Schizophrenia". The objectives of this 12-week study are to evaluate the efficacy, safety, and tolerability of AVP-786 as an adjunctive treatment compared with placebo in patients with residual schizophrenia.
What is the current status of trial NCT02477670?
This trial is currently completed. It is a Phase 2 study. The enrollment target is 145 participants. The study started on 2015-09. Estimated completion is 2017-07-21.
What conditions does trial NCT02477670 study?
This clinical trial studies the following conditions: Schizophrenia. These conditions were identified from the trial registry and reflect the primary focus areas of the research.
What interventions are being tested in trial NCT02477670?
The interventions under investigation include: Placebo (DRUG), AVP-786 (DRUG). Each intervention is being evaluated for safety and efficacy as part of this clinical study.
Who is sponsoring clinical trial NCT02477670?
This trial is sponsored by Avanir Pharmaceuticals, which has 4 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.
Where is trial NCT02477670 being conducted?
This trial has 17 study locations across California, District of Columbia, Florida, Georgia, Illinois. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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