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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00034801
Other study ID # 5529
Secondary ID F1D-US-HGJU
Status Completed
Phase Phase 4
First received May 2, 2002
Last updated July 18, 2006
Start date September 2001
Est. completion date March 2003

Study information

Verified date July 2006
Source Eli Lilly and Company
Contact n/a
Is FDA regulated No
Health authority United States: Food and Drug Administration
Study type Interventional

Clinical Trial Summary

This is a research study comparing the safety and efficacy of two active study medications


Recruitment information / eligibility

Status Completed
Enrollment 378
Est. completion date March 2003
Est. primary completion date
Accepts healthy volunteers No
Gender Both
Age group 18 Years to 60 Years
Eligibility Inclusion Criteria:

- Male or female subjects 18-60 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 Criteria:

- Treatment with a drug within the last 30 days that has not received regulatory approval at the time of study entry

- Female subjects who are either pregnant or nursing

- Uncorrected hypothyroidism or hyperthyroidism

- Narrow-angle glaucoma

Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double-Blind, Primary Purpose: Treatment


Intervention

Drug:
olanzapine

ziprasidone


Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Eli Lilly and Company

Country where clinical trial is conducted

United States, 

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