Expired Study
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Saint Charles, Missouri 63301


Purpose:

The objective of this study was the bioequivalence of a Roxane Laboratories' terbinafine tablets, 250 mg, to Lamisil® Tablets, 250 mg (Novartis Pharmaceutical Corporation.) under fed conditions using a single-dose, randomized, 2-treatment, 2-period, 2-sequence crossover design.


Criteria:

Inclusion Criteria: - No clinically significant abnormal findings on the physical examination, medical history, or clinical laboratory results during screening. Exclusion Criteria: - Positive test for HIV, Hepatitis B, or Hepatitis C. - Treatment with known enzyme altering drugs. - History of allergic or adverse response to terbinafine or any comparable or similar product.


NCT ID:

NCT00602251


Primary Contact:

Principal Investigator
Steven Herrmann, MD
Cetero Research, San Antonio


Backup Contact:

N/A


Location Contact:

Saint Charles, Missouri 63301
United States



There is no listed contact information for this specific location.

Site Status: N/A


Data Source: ClinicalTrials.gov

Date Processed: March 16, 2018

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