CompletedNCT02418819
A Study To Examine Safety, Pharmacokinetics, And Pharmacodynamic Of Pf 06412562 In Subjects With Schizophrenia
Medication studyAges 18–45United States
Understand this study
Who was this study for?
This study was for people with schizophrenia. Listed age limits: 18 years to 45 years. Other eligibility criteria applied.
- Listed locations
- Arcadia and 5 more locationsSee all locations and recruitment
- Study phase
- Phase 1Usually an early study focused on safety, tolerability, dosage, and side effects.
Study information
Study start dateStarted: April 2015
- Recruitment status
- Completed
- Enrollment listed in the registry
- 103
- Sponsor
- Pfizer
- Sponsor type
- Unknown or unclear
- Study type
- Drug
- Intervention type
- Medication / drug, OTHER
- Study phase
- Phase 1Usually an early study focused on safety, tolerability, dosage, and side effects.
- Locations
- United States
- Age range
- From 18 Years to 45 Years
- Official registry ID
- NCT02418819
- Official title
Show the full official title
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
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Recruitment & locations
CompletedArcadia · Glendale · Baltimore
2 more locations
- Gaithersburg
- Rockville
Questions about this study
Who is behind this study?
The study sponsor is Pfizer.
Did this study involve medication?
Yes. The study involved medication, including PF-06412562 3mg BID, PF-06412562 9mg BID and PF-06412562 45mg BID.
Who was this study for?
This study was for people with schizophrenia. Listed age limits: 18 years to 45 years. Other eligibility criteria applied.
