To Demonstrate the Relative Bioavailability of Desipramine Hydrochloride 50 mg Tablets

To demonstrate the relative bioavailability of Desipramine Hydrochloride 50 mg tablets.

Completed

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Key information

Conditions

Depression Behavior Behavioral Symptoms

Age range

19 year–50 year

Sex eligibility

Male

Study type

Interventional

Phase

Phase 1

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

No clinically significant abnormal finding on physical exam, medical history, or clinical laboratory results on screening.

Exclusion criteria

Positive test results for HIV or hepatitis B or C.
Treatment for drug or alcohol dependence.

Treatment and study plan

Desipramine Hydrochloride 50 mg Tablets (Cord Laboratories)

Drug

Desipramine Hydrochloride 50 mg Tablets (Merrell Dow Pharmaceuticals, Inc)

Drug

Primary outcomes

Bioequivalence based on AUC and Cmax

Time frame: 28 days

Sponsors and collaborators

Lead sponsor

Sandoz

Industry

Registry information

Official study title

Randomized, 2-way Crossover Bioavailability Study of Desipramine Hydrochloride 50 mg Tablets

Important dates

Study start: 1987
Primary completion: 1987
Study completion: 1987
First posted: Jun 4, 2009
Registry last updated: Mar 28, 2017

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.

Completed