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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00946387
Other study ID # B043712
Secondary ID
Status Completed
Phase Phase 1
First received July 24, 2009
Last updated March 27, 2017
Start date September 2004
Est. completion date September 2004

Study information

Verified date July 2009
Source Sandoz
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

To demonstrate the relative bioavailability study of Ondansetron HCl 24 mg tablets under fasting conditions.


Recruitment information / eligibility

Status Completed
Enrollment 26
Est. completion date September 2004
Est. primary completion date September 2004
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 22 Years to 58 Years
Eligibility Inclusion Criteria:

- No clinically significant abnormal finding on physical exam, medical history, or clinical laboratory results on screening.

Exclusion Criteria:

- Positive test results for HIV or hepatitis B or C.

- Treatment for drug or alcohol dependence.

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
Ondansetron HCl 24 mg Tablets (Sandoz, Inc.)

Zofran (Ondansetron HCl) 24 mg Tablets (GlaxoSmithKline)


Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Sandoz

Outcome

Type Measure Description Time frame Safety issue
Primary Bioequivalence based on AUC and Cmax 9 days
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