Clinical Trials Directory

Trials / Completed

CompletedNCT00960479

Relative Bioavailability Study of Ribavirin 200 Capsules and Rebetol 200 mg Capsules in Females Under Fasting Conditions

A Relative Bioavailability Study of Ribavirin (Geneva Pharmaceutical Technology Corporation, N.J., U.S.A.) 200 Capsules and Rebetol (Schering Corporation, N.J., U.S.A.) 200 mg Capsules in Females Under Fasting Conditions.

Status
Completed
Phase
Phase 1
Study type
Interventional
Enrollment
38 (actual)
Sponsor
Sandoz · Industry
Sex
Female
Age
18 Years – 65 Years
Healthy volunteers
Accepted

Summary

The purpose of this study is to demonstrate the relative bioavailability of Ribavirin 200 capsules and Rebetol 200 mg capsules in females under fasting conditions.

Conditions

Interventions

TypeNameDescription
DRUGRibavirin 200 mg Oral Capsule (Geneva Pharmaceutical, U.S.A.)
DRUGRebetol 200 mg Oral Capsule (Schering Corporation, U.S.A.)

Timeline

Start date
2001-01-01
Primary completion
2001-02-01
Completion
2001-02-01
First posted
2009-08-17
Last updated
2017-03-28

Source: ClinicalTrials.gov record NCT00960479. Inclusion in this directory is not an endorsement.

Relative Bioavailability Study of Ribavirin 200 Capsules and Rebetol 200 mg Capsules in Females Under Fasting Conditions (NCT00960479) · Clinical Trials Directory