To Demonstrate the Relative Bioavailability of Desipramine Hydrochloride Tablets

Phase 1CompletedNCT00913822

Sandoz36 enrolled

Overview

To demonstrate the relative bioavailability of Desipramine Hydrochloride tablets.

Study Type

INTERVENTIONAL

Allocation

RANDOMIZED

Purpose

TREATMENT

Masking

NONE

Enrollment

Conditions

Depression

Interventions

Desipramine Hydrochloride 100 mg Tablets (Cord Laboratories)DRUG

Norpramin 100 mg Tablets (Merrell Dow Pharmaceuticals, Inc.)DRUG

Eligibility

Sex: MALEMin age: 18 YearsMax age: 40 YearsHealthy volunteers:

Medical Language ↔ Plain English

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.

Outcomes

Primary Outcomes

Bioequivalence based on AUC and Cmax

Time frame: 22 days

Data from ClinicalTrials.gov

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