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Bioequivalence Study of Amlodipine / Losartan/ Hydrochlorothiazide of PHARMALINE, Lebanon Under Fastion Conditions

Information source: Pharmaceutical Research Unit, Jordan
ClinicalTrials.gov processed this data on August 23, 2015
Link to the current ClinicalTrials.gov record.

Condition(s) targeted: Fasting

Intervention: Amlodipin, losartan, HCTZ (Drug)

Phase: Phase 1

Status: Completed

Sponsored by: Pharmaceutical Research Unit, Jordan

Official(s) and/or principal investigator(s):
Rana .T Bustami, Phd.pharmacy, Principal Investigator, Affiliation: PRU

Summary

To assess the bioequivalence of the investigational TEST product with the marketed REFERENCE products by measurement of Plasma concentrations of Amlodipine ,Losartan, Carboxylic acid losartan metabolite & Hydrochlorothiazide in plasma and calculation of the bioequivalence parameters from those measurements followed by ANOVA and 90% confidence interval statistical evaluation.

Clinical Details

Official title: Comparative, Randomized,, Single Dose, Open-label, Crossover Bioequivalence Study of LOSANET AM PLUS 10mg/100mg/12.5 mg Tablets (One Tablet) of (PHARMALINE, Lebanon) Versus NORVASC 10mg Tablets (One Tablet) of (Pfizer Canada Inc., Kirkland (Quebec)) and HYZAAR 100mg/12.5 Tablets (One Tablet) of (Merck Sharp & Dohme, Quimica de Puerto Rico, Inc, Road 2 Km. 60.3, Sabana Hoyos, Arecibo, PR 00688 for Merck Sharp & Dohme B.V. Haarlem, The Netherlands) in Healthy Subjects Under Fasting Conditions.

Study design: Allocation: Randomized, Endpoint Classification: Bio-equivalence Study, Intervention Model: Crossover Assignment, Masking: Open Label, Primary Purpose: Treatment

Primary outcome: To assess the bioequivalence of Test oral formulation of LOSANET AM PLUS versus References NORVASC and HYZAAR.

Eligibility

Minimum age: 18 Years. Maximum age: 50 Years. Gender(s): Male.

Criteria:

Inclusion Criteria: 1. Healthy subjects. 2. Ethnic Group: Arab & Mediterranean 3. Race: Mixed skin (white & black skin people). 4. Age 18-50 years 5. Body-mass index 18. 5 to 30. 0 kg/m2 inclusive (minimum of 50 kg weight). 6. Subject is available for the whole study period and gave written informed consent 7. Physical examination within normal ranges 8. All laboratory screening results within the normal range, or being assessed as clinically non-significant by the attending physician 9. Vital signs within normal ranges. 10. Kidney function test, Liver function test should be within normal ranges. 11. Pre dosing blood pressure more than 110/70 mmHg. Exclusion Criteria: 1. Women of childbearing potential, pregnant and lactating women. 2. Ethnic Group (Non- Arab &/ or Non- Mediterranean) 3. History of severe allergy or allergic reactions to study drug or related drugs or heparin 4. Known history or presence of food allergies, or any surgical or medical condition known to interfere with the absorption, distribution, metabolism or excretion of drugs 5. History of serious illness that can impact fate of drugs 6. Known history or presence of cardiac, pulmonary, gastrointestinal, endocrine, musculoskeletal, neurological, hematological, liver or kidney disease, unless judged not clinically significant by the Principal Investigator, or medical designate 7. Clinically significant illness 4 weeks before study Period I 8. Serious mental disease, drug, alcohol, solvents or caffeine abuse, smoking. 9. Regular use of medication 10. Having taken medication that could affect the investigated drug product: a) Regular consumption of drugs during the two weeks prior to study initiation day, b) consumption of enzyme stimulating or inhibiting drugs (e. g. Barbiturates, Carbamazepine, Phenytoin, Amphetamine, benzodiazepine, cannabinoid, cocaine, opiates, phencyclidine, and methadone) during one month before the study initiation 11. Presence of any significant physical or organ abnormality 12. Donation of 1) at least 400 ml of blood within 60 days, or 2) more than 150 ml of blood within 30 days, or 3) more than 100 ml blood plasma or platelets within 14 days before study Period I 13. Participation in another bioequivalence study within 80 days prior to the start of this study Period I 14. Following a special diet (e. g. vegetarian) or dieting one month before the study initiation. 15. Prior history of hypersensitivity to Amlodipine besylate, Losartan Potassium & Hydrochlorothiazide. 16. Consumption of grapefruit or grapefruit containing products within 7 days of drug administration 17. Ingestion of any vitamins or herbal products within 7 days prior to the initial dose of the study medication. 18. Exhausting physical exercise in the last 48 hours (e. g. weight lifting) or any recent significant change in dietary or exercise habits. 19. Any significant clinical abnormality including HBsAg, HCV, and HIV 20. Abnormal vital signs. 21. Abnormal Kidney or Liver function tests. 22. Vomiting, Diarrhea. 23. Pre dosing blood pressure less than 110/70 mmHg 24. Positive test for elicit drugs and alcohol prior to dosing in each period.

Locations and Contacts

Pharmaceutical research unit, Amman 1084, Jordan
Additional Information

Starting date: October 2012
Last updated: July 24, 2013

Page last updated: August 23, 2015

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