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

NCT ID: NCT01713647

Last Updated: 2013-07-25

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: PHASE1
• Total Enrollment: 39 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2012-10-31
• Study Completion Date: 2012-12-31

Brief 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.

Conditions

Fasting

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: CROSSOVER
• Primary Study Purpose: TREATMENT
• Blinding Strategy: NONE

Study Groups

LOSANET AM PLUS (10/100/12.5 mg) of PHARMALINE, Lebanon

Subjects will be fasted overnight and receive one tablet by mouth in accordance with randomization table, and blood samples will be taken at specified intervals over 3 days

intervention: Drug: LOSANET AM PLUS Amlodipine/ Losartan/Hydrochlorothiazide Other Name: NA

Group Type: EXPERIMENTAL

Amlodipin, losartan, HCTZ

Intervention Type: DRUG

NORVASC & HYZAAR (100/12.5 mg)

Subjects will be fasted overnight and receive one tablet of Norvasc &HYZAAR by mouth in accordance with randomization table, and blood samples will be taken over 3 days

intervention: Drug: LOSANET AM PLUS Amlodipine/ Losartan/Hydrochlorothiazide Other Name: NA

Group Type: ACTIVE_COMPARATOR

Amlodipin, losartan, HCTZ

Intervention Type: DRUG

Interventions

Amlodipin, losartan, HCTZ

Intervention Type: DRUG

Other Intervention Names

LOSANET AM PLUS

Eligibility 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.

• Minimum Eligible Age: 18 Years
• Maximum Eligible Age: 50 Years
• Eligible Sex: MALE
• Accepts Healthy Volunteers: Yes

Sponsors

Pharmaceutical Research Unit, Jordan

OTHER

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Rana .T Bustami, Phd.pharmacy

Role: PRINCIPAL_INVESTIGATOR

PRU

Locations

Pharmaceutical research unit

Amman, Amman Governorate, Jordan

Countries

Jordan

Other Identifiers

AMLH423/PRO-00

Identifier Type: -

Identifier Source: org_study_id