Bioequivalence Study of Doxycycline Monohydrate Tablets Under Fasting Conditions

To Determine Bioequivalence Under Fasting Conditions Clinical Trial

Official title:
Randomized, 2-way Crossover, Comparative Bioequivalence Study of Par Pharmaceutical Inc. (USA) and Oclassen Pharmaceuticals Inc. (USA) (Monodox(R)) Doxycycline Monohydrate Equivalent to 100 mg Doxycycline Administered as a Single Dose of 100 mg In Healthy Adult Males Under Fasting Conditions

Status Completed

Clinical Trial Summary

The purpose of this study is to compare the single-dose bioequivalence of Par and Oclassen doxycycline monohydrate, 100 mg.

Clinical Trial Description

To compare the single-dose bioequivalence of Par and Oclassen (Monodox(R)), 100 mg doxycycline under fasting conditions. ;

Study Design

Allocation: Randomized, Endpoint Classification: Bio-equivalence Study, Intervention Model: Crossover Assignment, Masking: Open Label

Related Conditions & MeSH terms

Disease
To Determine Bioequivalence Under Fasting Conditions

Clinical Trial Details

NCT number	NCT01380483
Study type	Interventional
Source	Par Pharmaceutical, Inc.
Contact
Status	Completed
Phase	Phase 1
Start date	January 2000
Completion date	April 2000

View Details

See also
Status	Clinical Trial	Phase
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Completed	`NCT00653419` - Bioavailability Study of (Buspar) Buspirone HCl Tablets Under Fasting Conditions	Phase 1
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