Expired Study
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Austin, Texas 78759


Purpose:

The objective of this study was to prove the bioequivalence of Ramipril 10 mg capsules under fed conditions.


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 Ramipril or any comparable or similar product.


NCT ID:

NCT00702260


Primary Contact:

Principal Investigator
Daniel V Freeland, D.O.
CEDRA Clinical Research


Backup Contact:

N/A


Location Contact:

Austin, Texas 78759
United States



There is no listed contact information for this specific location.

Site Status: N/A


Data Source: ClinicalTrials.gov

Date Processed: January 22, 2018

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