A Study of Cariprazine in Patients With Chronic Stable Schizophrenia

Part of paid clinical trials in Costa Mesa, California.

Sponsor
Forest Laboratories
Study ID
NCT00839852
Phase
PHASE2
Status
Completed

Conditions

Eligibility Criteria

Sex
ALL
Age
18 Years - 61 Years
Healthy Volunteers
Not accepted

Interventions

  • Cariprazine — DRUG
    Cariprazine was supplied in capsules.

Study Details

This is an outpatient study to evaluate the long-term safety, tolerability, and pharmacokinetics of cariprazine in patients with schizophrenia.

Key Dates

Start date
May 31, 2009
Status verified
Aug 2019
Primary completion
Aug 31, 2010
Completion
Aug 31, 2010

Study Design

Enrollment
97 participants (actual)
Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT

Arms

  • Experimental: Cariprazine 1.5mg
    Participants received cariprazine 1.5 mg capsule once, twice or three times a day depending on their response and tolerability

Primary Outcome Measure

Change From Baseline to Week 48 in the PANSS Total Score [ Time Frame: Baseline to Week 48 ]

Locations (17)

FacilityCityStateZIPSite coordinators
Forest Investigative SiteCosta MesaCalifornia92626-
Forest Investigative SiteLong BeachCalifornia90813-
Forest Investigative SiteOceansideCalifornia92056-
Forest Investigative SiteParamountCalifornia90723-
Forest Investigative SiteRiversideCalifornia92506-
Forest Investigative SiteWashington D.C.District of Columbia20016-
Forest Investigative SiteBradentonFlorida34208-
Forest Investigative SiteKissimmeeFlorida34741-
Forest Investigative SiteLake CharlesLouisiana70601-
Forest Investigative SiteBaltimoreMaryland21202-
Forest Investigative SiteFlowoodMississippi39232-
Forest Investigative SiteCreve CoeurMissouri63141-
Forest Investigative SiteCincinnatiOhio45267-
Forest Investigative SiteCharlestonSouth Carolina29405-
Forest Investigative SiteMemphisTennessee38119-
Forest Investigative SiteHoustonTexas77008-
Forest Investigative SiteIrvingTexas75062-

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