Status:

COMPLETED

Relative Bioavailability Study of Nadolol (1 x 80 mg) Tablets Under Fasting Conditions

Lead Sponsor:

Sandoz

Conditions:

High Blood Pressure

Migraine Headaches

Eligibility:

MALE

18-40 years

Phase:

PHASE1

Brief Summary

The purpose of this study is to demonstrate the relative bioavailability of Nadolol (1 x 80 mg) tablets under fasting conditions.

Eligibility Criteria

Inclusion

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

Exclusion

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

Key Trial Info

Start Date :

July 1 1994

Trial Type :

INTERVENTIONAL

Allocation :

ACTUAL

End Date :

July 1 1994

Estimated Enrollment :

34 Patients enrolled

Trial Details

Trial ID

NCT00960245

Start Date

July 1 1994

End Date

July 1 1994

Last Update

March 28 2017

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Relative Bioavailability Study of Nadolol (1 x 80 mg) Tablets Under Fasting Conditions | DecenTrialz