Bioavailability Study of Amlodipine Besylate/Atorvastatin Calcium Tablets 10/80 mg Under Fasting Condition

Overview

This study is to assess the bioequivalence between Amlodipine besylate/Atorvastatin calcium Tablets 10mg/80mg of Dr. Reddy's Laboratories Limited, India and CADUET® (amlodipine besylate and atorvastatin calcium) tablets 10mg/80mg of Pfizer Ireland Pharmaceuticals Dublin, Ireland in Healthy Male and Female Volunteers under Fasting conditions.

Full Title of Study: “Open Label, Randomized, Two-treatment, Two-period, Two-sequence,Crossover, Single Dose, Oral Bioequivalence Study of Amlodipine Besylate/Atorvastatin Calcium Tablets 10mg/80mg Under Fasting Condition”

Study Type

  • Study Type: Interventional
  • Study Design
    • Allocation: Randomized
    • Intervention Model: Crossover Assignment
    • Primary Purpose: Treatment
    • Masking: None (Open Label)
  • Study Primary Completion Date: October 2011

Detailed Description

Open label, randomized, two-treatment, two-period, two-sequence, crossover, single dose, oral bioequivalence study of Amlodipine besylate/Atorvastatin calcium Tablets 10mg/80mg under Fasting conditions.

Interventions

  • Drug: Amlodipine besylate/Atorvastatin calcium
    • Amlodipine besylate/Atorvastatin calcium 10/80 mg

Arms, Groups and Cohorts

  • Experimental: Amlodipine besylate/Atorvastatin calcium tablets 10/80 mg
    • Amlodipine besylate/Atorvastatin calcium tablets 10/80 mg of Dr. Reddys Laboratories Limited
  • Active Comparator: Caduet
    • Caduet® 10/80 mg tablets of Pfizer, Ireland

Clinical Trial Outcome Measures

Primary Measures

  • Area under curve (AUC)
    • Time Frame: 0.50; 1.00; 2.00; 3.00; 4.00; 5.00; 6.00; 7.00; 8.00; 10.00; 11.00; 12.00 16.00; 24.00; 36.00;48.00 and 72.00 hours post dose for Amlodipine

Secondary Measures

  • Area under curve (AUC)
    • Time Frame: 10 min; 20 min; 30 min; 40 min; 50 min; 1.00; 1.25; 1.50; 1.75; 2.00; 2.25; 2.50; 2.75; 3.00; 3.50; 4.00; 4.50; 5.00; 6.00; 8.00; 10.00; 12.00 16.00;24.00; 36.00; 48.00 and 72.00 hours post dose for Atorvastatin

Participating in This Clinical Trial

Inclusion Criteria

1. Healthy male and female volunteers between 18 and 55 years of age 2. Subject with the Body Mass Index within 18.5 and 24.9 kg/m2, weight not less than 50 kg 3. Normal health as determined by personal medical history, haematology, clinical chemistry and urinalysis laboratory profiles 4. Non smokers or ex-smokers that gave up smoking for at least two years prior to the study 5. The subject agrees to abstain from alcohol, food and drinks containing methylxanthines (tea, cola, chocolate) for 48 hours prior to study drug administration and during each study period and from grapefruit-containing food and beverages for 48 hours prior to study drug administration and during each study period 6. Ability to understand the full nature and purpose of the study, including possible risks and side effects; ability to cooperate with the Clinical Investigator and to comply with the requirements of the entire study 7. Informed written consent given voluntary before the initiation of the pre-study screening 8. Negative results to the HIV, hepatitis C or hepatitis B test 9. Negative results from pregnancy tests (for female subjects only) 10. Non-lactating woman (for female subjects only) 11. Subjects using non-hormonal contraceptive measures during the study (for female subjects only) 12. Normal creatine phosphokinase (CPK) levels at the time of check-in of each period. Exclusion Criteria:

1. History of hypersensitivity to the test drug (Amlodipine Besylate/Atorvastatin Calcium) or to drugs belonging to the same pharmacological and chemical class and inactive ingredients of the formulation 2. Participation in a clinical study with an investigational product in the preceding three months or in a clinical study with a generic product in the preceding two months 3. Hospitalization for any reason within eight weeks prior to the study initiation 4. Donation of 450 ml or more of blood, within eight weeks prior to the study initiation 5. Intake of any prescription or non-prescription drug (including anti-acids, analgesics, statins, cyclosporin, fibric acid derivatives, erythromycin, azole antifungals, niacin, oral contraceptives etc.) during the two weeks preceding the study or throughout the study 6. History of presence of any relevant medical condition including cancer, significant disease of the renal, hepatic, immunological, dermatological, gastrointestinal, respiratory, cardiovascular, endocrine or locomotor systems, and any metabolic, haematological neurological disorder or psychiatric disorder 7. History or presence of drug or alcohol abuse, within the past year 8. History or any current condition or other disease known to interfere with the absorption, distribution, metabolism or excretion of investigational medicines 9. ECG having evidence of clinically significant abnormalities 10. Presence of any acute or chronic infectious disease 11. Positive results to the HIV, hepatitis C or hepatitis B tests 12. Positive results to the breath alcohol test and drugs of abuse checks 13. Positive results to the pregnancy tests (for female subjects only) 14. Subject is vegetarian or follows particular diets 15. A history of difficulty with donating blood.

Gender Eligibility: All

Minimum Age: 18 Years

Maximum Age: 55 Years

Are Healthy Volunteers Accepted: Accepts Healthy Volunteers

Investigator Details

  • Lead Sponsor
    • Dr. Reddy’s Laboratories Limited
  • Provider of Information About this Clinical Study
    • Sponsor
  • Overall Official(s)
    • Dr. V Parasca, MD, Principal Investigator, 3S-Pharmacological Consultation & Research GmbH

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