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Trials / Completed

CompletedNCT00659685

Bioavailability Study of Ondansetron 16 mg Orally Disintegrating Tablets Under Fasting Conditions

Comparative, Randomized, Single-Dose, Cross Over Bioavailability of Kali's Ondansetron 16 mg ODT With That of GlaxoSmithKine's Zofran 16 mg ODT in Healthy, Male and Female Subjects Under Fasting Conditions

Status
Completed
Phase
Phase 1
Study type
Interventional
Enrollment
24 (actual)
Sponsor
Par Pharmaceutical, Inc. · Industry
Sex
All
Age
18 Years – 55 Years
Healthy volunteers
Accepted

Summary

Single-dose cross over comparative bioavailability of Ondansetron 16 mg ODT and Zofran 16 mg ODT

Detailed description

To Compare the single-dose bioavailability of Kali's Ondansetron 16 mg ODT with that of GlaxoSmithKine's Zofran 16 mg ODT under fasting conditions

Conditions

Interventions

TypeNameDescription
DRUGOndansetronODT, single-dose, fasting
DRUGZofran ODT

Timeline

Start date
2003-11-01
First posted
2008-04-16
Last updated
2008-04-16

Locations

1 site across 1 country: Canada

Source: ClinicalTrials.gov record NCT00659685. Inclusion in this directory is not an endorsement.

Bioavailability Study of Ondansetron 16 mg Orally Disintegrating Tablets Under Fasting Conditions (NCT00659685) · Clinical Trials Directory