CI

At a glance

ClinicalIndex Comparison Record
Phase 2Completed· 71 enrolled
Drug / intervention
PF-03463275 +1 moredrug
Likely dose
Not stated in 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/NCT01911676
NCT01911676Phase 2Completed

Translational Neuroscience Optimization of GlyT1 Inhibitor

Yale University·interventional·Posted Jul 30, 2013·Updated Aug 19, 2024

In Brief

A Phase 2 clinical trial evaluating PF-03463275 and Placebo for Cognitive Impairments Associated With Schizophrenia. Completed, enrolled 71 participants across 2 sites.

Detailed Summary

This is a Phase II, randomized, double-blind, placebo-controlled, cross-over POC study of stable patients with Schizophrenia or Schizoaffective disorder. The primary objective of this study is to test the efficacy of treatment with one of two does of a glycine transporter inhibitor (GlyT1I) combined with cognitive remediation to enhavce cognitive function. Subjects will be randomized to one of two doses of the glycine transporter inhibitor (GlyT1I) and placebo twice daily in addition to their antipsychotic medication for 2 treatment periods, each lasting a minimum of 5 weeks. Treatment periods will be separated by a washout period lasting approximately 3 weeks.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesUnited States

Timeline

Phase 2CompletedFinished
2014201520162017201820192020202120222023202420252026
First PostedJul 30, 2013
Enrollment StartAug 1, 2013
Primary CompletionDec 1, 2018
TodayJul 2, 2026
Enrollment to primary: 5.3 yearsPosted 12.9 years ago

Interventions

PF-03463275drug

Placebodrug