Bioequivalence Study Doxycycline Tablets and Monodox Capsules Under Fasting Conditions

To Determine Bioequivalence Under Fasting Conditions Clinical Trial

Official title:
Randomized, 2-Way Crossover, Bioequivalence Study of Doxycycline 150 mg Tablet and Monodox 50 mg Capsule Administered as 1 x 150 mg Tablet or 3 x 50 mg Capsules in Healthy Subjects Under Fasting Conditions

Status Completed

Clinical Trial Summary

To compare the rate and extent of absorption of doxycycline tablet (Par) versus doxycycline capsule (Monodox)(Oclassen).

Clinical Trial Description

To compare the rate and extent of absorption of doxycycline 150 mg tablet (test) versus Monodox 50 mg capsule (reference) administered as 1 x 50 mg tablet or 3 x 50 mg capsules 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	NCT00652795
Study type	Interventional
Source	Par Pharmaceutical, Inc.
Contact
Status	Completed
Phase	Phase 1
Start date	July 2004
Completion date	September 2004

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
Completed	`NCT01380457` - Bioavailability Study of Dronabinol Capsules 10 mg Under Fasting Conditions	Phase 1
Completed	`NCT01380483` - Bioequivalence Study of Doxycycline Monohydrate Tablets Under Fasting Conditions	Phase 1
Completed	`NCT00652639` - Bioavailability Study of Clonazepam Tablets Under Fasting Conditions	Phase 1
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