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Olanzapine Versus Active Comparator in the Treatment of Bipolar I Disorder

Phase 4
Completed
Conditions
Bipolar Disorder
Registration Number
NCT00034580
Lead Sponsor
Eli Lilly and Company
Brief Summary

This is a research study comparing the safety and efficacy of two active study medications for the treatment of bipolar I disorder.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
326
Inclusion Criteria
  • Male or female subject, 18-70 years of age
  • Female subjects of childbearing potential must be using a medically accepted means of contraception
  • Each subject must have a level of understanding sufficient to perform all tests and examinations required by the protocol
  • Subjects must be considered reliable

Exclusion:

  • Female subjects who are either pregnant or nursing
  • Uncorrected hypothyroidism or hyperthyroidism
  • Narrow-angle glaucoma
  • Subjects who present a serious and immediate risk of endangering him or herself
Exclusion Criteria

Not provided

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod
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