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Clinical Trials/JPRN-jRCT2080220563
JPRN-jRCT2080220563
Unknown
Phase 3

Randomized, Placebo-controlled, Double-blind, Parallel-group, Confirmatory Study of SM-13496 (lurasidone HCl) in Patients with Schizophrenia <Phase III Study>

Sumitomo Dainippon Pharma Co., Ltd.0 sites460 target enrollmentJune 9, 2008
ConditionsSchizophrenia

Overview

Phase
Phase 3
Intervention
Not specified
Conditions
Schizophrenia
Sponsor
Sumitomo Dainippon Pharma Co., Ltd.
Enrollment
460
Last Updated
2 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
June 9, 2008
End Date
TBD
Last Updated
2 years ago
Study Type
Interventional
Sex
All

Investigators

Eligibility Criteria

Inclusion Criteria

  • \- Patient meets DSM\-IV criteria for schizophrenia.
  • \- Patient is 18 or older but younger than 75 years of age on the day of signing informed consent.
  • \- Patient understands the objectives, nature, and other aspects of the study and voluntarily agrees to participate in the study by providing written informed consent.

Exclusion Criteria

  • \- Patient has a history of neuroleptic malignant syndrome, water intoxication, or paralytic ileus.
  • \- Patient has Parkinson's disease.
  • \- Patient has a history or complication of malignancy.

Outcomes

Primary Outcomes

Not specified

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