Expired Study
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Saint Charles, Missouri 63301


The objective of this study was the bioequivalence of a Roxane Laboratories' Amlodipine Besylate tablets, 10 mg, to Norvasc® Tablets, 10 mg (Pfizer) under fasting conditions using a single-dose, randomized, 2-treatment, 2-period, 2-sequence crossover design.


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 Amlodipine Besylate or any comparable or similar product.

Study is Available At:

Original ID:




Secondary ID:

Study Acronym:

Brief Title:

Bioequivalency Study of Amlodipine Tablets Under Fasting Conditions

Official Title:

A Single Dose, Two-Period, Two-Treatment, 2-Way Crossover Bioequivalency Study of 10 mg Amlodipine Besylate Tablets Under Fasting Conditions

Overall Status:


Study Phase:




Minimum Age:

18 Years

Maximum Age:

45 Years

Quick Facts

Healthy Volunteers
Oversight Has DMC
Study Is FDA Regulated
Study Is Section 801
Has Expanded Access

Study Source:

West-Ward Pharmaceutical

Oversight Authority:

United States: Food and Drug Administration

Reasons Why Stopped:

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Study Design:

Number of Arms:


Number of Groups:


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Overall Contact Information

Official Name:Steven Herrmann, MD
Principal Investigator
Cetero Research, San Antonio

Study Dates

Start Date:April 2004
Completion Date:May 2004
Completion Type:Actual
Primary Completion Date:May 2004
Primary Completion Type:Actual
Verification Date:January 2018
Last Changed Date:January 19, 2018
First Received Date:January 15, 2008

Study Outcomes

There are no available Study Outcomes

Study Interventions

Intervention Type:Drug

Study Arms

There are no available Study Arms

Study Agencies

Agency Class:Industry
Agency Type:Lead Sponsor
Agency Name:Roxane Laboratories

Sample and Retention Information

There are no available Sample and Retention Information

Study References

There are no available Study References

Data Source: ClinicalTrials.gov

Date Processed: October 09, 2019

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