At a glance
ClinicalIndex Comparison RecordPhase 1Completed· 103 enrolled
Drug / intervention
PF-06412562 3mg BID +3 moredrug
Likely dose
PF-06412562 3mg BIDfrom 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.
A RANDOMIZED, DOUBLE-BLIND, PLACEBO CONTROLLED, PARALLEL GROUP, SPONSOR OPEN, PHASE 1B STUDY TO EXAMINE THE SAFETY, TOLERABILITY, PHARMACOKINETICS, AND PHARMACODYNAMICS OF PF-06412562 IN PSYCHIATRICALLY STABLE SUBJECTS WITH SCHIZOPHRENIA
In Brief
A Phase 1 clinical trial evaluating PF-06412562 3mg BID, PF-06412562 9mg BID, and 2 other interventions for Schizophrenia. Completed, enrolled 103 participants across 6 sites.
Detailed Summary
This study is designed to investigate the safety, tolerability pharmacokinetics and pharmacodynamic effects of PF-06412562 following multiple dose administration as MR tablets in subjects with schizophrenia.
Study Details
Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsSchizophrenia
CountriesUnited States
Collaborators--
Timeline
Phase 1CompletedFinished
201520162017201820192020202120222023202420252026
Enrollment StartApr 2015
First PostedApr 2015
Primary CompletionOct 2016
TodayJul 2026
First PostedApr 16, 2015
Enrollment StartApr 1, 2015
Primary CompletionOct 1, 2016
TodayJul 2, 2026
Enrollment to primary: 1.5 yearsPosted 11.2 years ago
Interventions
PF-06412562 3mg BIDdrug
PF-06412562
PF-06412562 9mg BIDdrug
PF-06412562
PF-06412562 45mg BIDdrug
PF-06412562
Placeboother
Placebo