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
| Type | Name | Description |
|---|---|---|
| DRUG | Ondansetron | ODT, single-dose, fasting |
| DRUG | Zofran 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.