Status:

COMPLETED

Bioequivalency Study of Levetiracetam 750 mg Tablets Under Fasting Conditions

Lead Sponsor:

Roxane Laboratories

Conditions:

Seizures

Eligibility:

FEMALE

18-45 years

Phase:

NA

Brief Summary

The objective of this study was to prove the bioequivalence of Levetiracetam 750 mg Tablets under fasted conditions

Eligibility Criteria

Inclusion

  • No clinically significant abnormal findings on the physical examination, medical history, or clinical laboratory results during screening

Exclusion

  • Positive test for HIV, Hepatitis B, or Hepatitis C. Treatment with known enzyme altering drugs. History of allergic or adverse response to Levetiracetam or any comparable or similar product.

Key Trial Info

Start Date :

August 1 2005

Trial Type :

INTERVENTIONAL

Allocation :

ACTUAL

End Date :

August 1 2005

Estimated Enrollment :

27 Patients enrolled

Trial Details

Trial ID

NCT00826865

Start Date

August 1 2005

End Date

August 1 2005

Last Update

January 23 2018

Active Locations (1)

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1

MDS Pharma Services

Phoenix, Arizona, United States, 85044