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CompletedNCT02477670

Efficacy, Safety, and Tolerability of AVP-786 for the Treatment of Residual Schizophrenia

This study evaluated the safety and effectiveness of AVP-786 for people with schizophrenia.

Medication studyAges 18–60United States
The study in practice

Understand this study

What did researchers investigate?

This study evaluated the safety and effectiveness of AVP-786 for people with schizophrenia.

Who was this study for?

This study was for people with schizophrenia. Listed age limits: 18 years to 60 years. Other eligibility criteria applied.

Listed locations
Cerritos, United States · Garden Grove, United States and 15 more locationsSee all locations and recruitment
Activities
Medication described in the protocol · Placebo comparator
Compensation
Payment and expense reimbursement have not been verified.
Study clarity

Study information

Study start dateStarted: September 1, 2015
Recruitment status
Completed
Enrollment listed in the registry
145
Sponsor
Otsuka Pharmaceutical Development & Commercialization, Inc.
Sponsor type
Pharmaceutical company
Study type
Drug
Intervention type
Medication / drug
Study phase
Phase 2Usually explores whether the intervention may work, while continuing to monitor safety.
Locations
United States
Age range
From 18 Years to 60 Years
Official registry ID
NCT02477670
Official title
Show the full official title

A Phase 2, Multicenter, Randomized, Double-blind, Placebo-controlled, Sequential Parallel Comparison Design (SPCD) Study to Assess the Efficacy, Safety and Tolerability of AVP-786 (Deuterated [d6]-Dextromethorphan Hydrobromide [d6-DM]/Quinidine Sulfate [Q]) as an Adjunctive Treatment for Patients With Residual Schizophrenia

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Recruitment & locations

Completed

Cerritos · Garden Grove · National City

14 more locations
  • Oakland
  • San Diego
  • Washington D.C.
  • Orlando
  • Atlanta
  • Augusta
  • Chicago
  • Boston
  • Worcester
  • Grand Rapids
  • Marlton
  • Jamaica
  • New York
  • Rochester
FAQ

Questions about this study

What did researchers investigate?

This study evaluated the safety and effectiveness of AVP-786 for people with schizophrenia.

Who is behind this study?

The study sponsor is Otsuka Pharmaceutical Development & Commercialization, Inc., a pharmaceutical company.

Did this study involve medication?

Yes. The study involved medication, including AVP-786 and Placebo.

Who was this study for?

This study was for people with schizophrenia. Listed age limits: 18 years to 60 years. Other eligibility criteria applied.

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