To Demonstrate the Relative Bioavailability of Atenolol Tablets, 100 mg

Phase 1CompletedNCT00946725

Sandoz28 enrolled

Overview

To demonstrate the relative bioavailability of atenolol tablets, 100 mg.

Study Type

INTERVENTIONAL

Allocation

RANDOMIZED

Purpose

TREATMENT

Masking

NONE

Enrollment

Conditions

Angina Hypertension

Interventions

Atenolol (Tenormin) 100 mg Tablets Zeneca (Astra Zeneca Pharmaceutical)DRUG

Atenolol 100 mg Tablets (Geneva Pharmaceutical, Inc.)DRUG

Eligibility

Sex: MALEMin age: 18 YearsMax age: 50 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: 20 days

Data from ClinicalTrials.gov

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