Bioequivalence Study of Fosinopril Sodium/ Hydrochlorothiazide 20/ 12.5 mg Tablets Under Fasting Conditions

Ranbaxy

Status

Completed

Conditions

Healthy

Treatments

Drug: Fosinopril sodium and hydrochlorothiazide 20-12.5 mg tablets

Study type

Interventional

Funder types

Industry

Identifiers

NCT00777972

B035501

Details and patient eligibility

About

The objective of this study was to compare the relative bioavailability of Fosinopril sodium and hydrochlorothiazide 20-12.5 mg tablets by Ranbaxy Laboratories Limited with that of Monopril ®.-HCT 20-12.5 mg tablets by Bristol-Meyers Squibb following a single oral dose (1 x 20-12.5 mg tablet) in healthy adult subjects under fasting conditions

Full description

This study was a single dose, randomized, two period, two treatment, two sequence crossover study design was used to evaluate the relative bioavailability of Fosinopril sodium and hydrochlorothiazide tablet products when dose (1 x 20-12.5 mg) under fasting conditions. The two periods of the study were separated by a washout period of at least a week.

A total of 36 healthy adult subjects were enrolled in the study. Of all the subjects 34 subjects (21 males and 13 females) completed the study.

Enrollment

34 patients

Sex

All

Ages

18+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

Subjects should be at least 18 years old
Female subjects with negative serum pregnancy test
Subject with no clinically significant abnormal lab values at the pre-entry evaluation
Subjects with negative or non-reactive urine drug of abuse, hepatitis B, hepatitis C and HIV screening
Subject has acceptable ECG
Subject has no evidence of underlying disease at the pre-entry physical examination
Subject has agreed to undergo at least a 14 day washout period for prescription drugs prior to the first dosing of the study and throughout the periods of blood sample collection
Subject has agreed to undergo at least a 7 day washout period for OTC products, herbal medications, etc. prior to the first dosing of the study medication and throughout the periods of blood sample collections
Subject agrees to abstain from consuming alcohol for at least 48 hours prior to each dosing and throughout the periods when blood samples are being obtained
Subject agrees to abstain from consuming grapefruit, grapefruit juice, or other foods containing grapefruit for at least 48 hours prior to each dosing and throughout the periods when blood samples are being obtained
Subject has given a written consent to participate

Exclusion criteria

Subject has a history of chronic alcohol consumption (during past 2 years) or drug addiction
Subject has a history of serious gastrointestinal, renal, hepatic or cardiovascular disease, tuberculosis, epilepsy, asthma (during past 5 years), diabetes, psychosis or glaucoma
Subject has a history of allergic responses to the class of drug being tested.
Subject has donated any blood and/ or plasma within the last thirty (30) days prior to the first dosing of the study
Subject has taken any investigational drug within thirty (30) days prior to the first dosing of the study
Female subjects who are pregnant, breast feeding, or likely to be come pregnant during the study. Female subjects of child bearing potential must either abstain from sexual intercourse or use a reliable barrier method (eg condom, IUD) of contraception during the course of the study (first dosing until the last blood collection)
Female subjects who have used implanted or injected hormonal contraceptives (except Lunelle ® Monthly Injection) anytime during the 6 months prior to study dosing, Lunelle ® Monthly Injection anytime during the 45 days prior to the study dosing, or used oral hormonal contraceptives within 14 days before dosing.
Subject with the inability to read and/ or sign the consent form