CI

At a glance

ClinicalIndex Comparison Record
Phase 2Completed· 403 enrolled
Drug / intervention
Pimavanserin +1 moredrug
Likely dose
Pimavanserin 34 mgfrom record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT02970305
NCT02970305Phase 2Completed

A Phase 2, Randomized, Double-Blind, Placebo-Controlled Study to Evaluate the Efficacy and Safety of Pimavanserin as Adjunctive Treatment for the Negative Symptoms of Schizophrenia

ACADIA Pharmaceuticals Inc.·interventional·Posted Nov 22, 2016·Updated Dec 22, 2020

In Brief

A Phase 2 clinical trial evaluating Pimavanserin and Placebo for Schizophrenia. Completed, enrolled 403 participants across 101 sites in 10 countries.

Detailed Summary

To evaluate the efficacy and safety of adjunctive pimavanserin compared with adjunctive placebo in the treatment of the negative symptoms of schizophrenia

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsSchizophrenia
CountriesBulgaria, Canada, Czechia, Hungary, Poland, Russia, Serbia, Spain, Ukraine, United States
Collaborators--

Timeline

Phase 2CompletedFinished
2017201820192020202120222023202420252026
First PostedNov 22, 2016
Enrollment StartNov 4, 2016
Primary CompletionOct 16, 2019
Study CompletionOct 28, 2019
TodayJul 2, 2026
Enrollment to primary: 2.9 yearsPosted 9.6 years ago

Interventions

Pimavanserindrug

Pimavanserin 34 mg, 20 mg, or 10 mg, taken as two tablets, once daily by mouth

Placebodrug

Placebo, taken as two tablets, once daily by mouth