Bioequivalence Study of Isotretinoin Capsules 40 mg Under Fed Condition

• Status: Completed
• Trial end date: 2001-06-01
• Target enrollment: 0
• Participant gender: Male

Summary

The purpose of this study is to determine the pharmacokinetics and bioequivalence of isotretinoin formulations after administration of single doses to normal, non-smoking,healthy males under fed conditions

• Phase: Phase 1
• Accepts Healthy Volunteers?: Accepts Healthy Volunteers

Details

• Lead Sponsor: Dr. Reddy's Laboratories Limited
• Treatments: Isotretinoin

Criteria

Inclusion Criteria:

1. Healthy males between 18 and 45 years of age inclusive.

2. Informed of the nature of the study and given written informed consent.

3. Have a body weight within 15% of the appropriate range as defined in the 1983 Metropolitan Life Company tables and weighing at least 125 lbs. (Appendix I).

Exclusion Criteria

1. Hypersensitivity to isotretinoin or related compounds.

2. Any history of a clinical condition which might affect drug absorption, metabolism or excretion.

3. Recent history of mental illness, drug addiction, drug abuse or alcoholism.

4. Donation of greater than 500 ml of blood in the past 4 weeks prior to study dosing or difficulty in donating blood.

5. Received an investigational drug within the 4 weeks prior to study dosing.

6. Currently taking any prescription medication within the 7 days prior to study dosing or over-the-counter medication within 3 days of study dosing. This prohibition does not include vitamins or herbal preparations taken as nutritional supplements for non-therapeutic indications as judged by the attending physician.

7. Regular tobacco use in the 3 months prior to study dosing.