Status:
COMPLETED
Bioequivalence Study of Fenofibrate 160mg Tablets Under Fed Conditions
Lead Sponsor:
Ranbaxy Laboratories Limited
Conditions:
Healthy
Eligibility:
All Genders
18-55 years
Phase:
NA
Brief Summary
The objective of this study was to compare the single-dose relative bioavailability of Ranbaxy and Abbott (TriCor) 160 mg fenofibrate tablets under fed conditions.
Detailed Description
This was an open-label, randomized, single-dose, 2-way crossover, relative bioavailability study performed on 24 healthy adult male and female volunteers A total of 23 subjects (16 males and 7 females...
Eligibility Criteria
Inclusion
- Subject candidates must fulfill the following inclusion criteria to be eligible for participation in the study, unless otherwise specified:
- Healthy adult male and female volunteers, 18-55 years of age;
- Weighing at least 52 kg for males and 45 kg for females and within 15% of their ideal weights (Table of "Desirable Weights of Adults", Metropolitan Life Insurance Company, 1983);
- Medically healthy subjects with no clinically abnormal laboratories and ECGs, as deemed by the principal investigator;
- Females of childbearing potential should either be sexually inactive (abstinent) for 14 days prior to the study and throughout the study or be using one of the following acceptable birth control methods:
- Surgically sterile (tubal ligation, hysterectomy, bilateral oophorectomy) 6 months minimum. Proof is required for the hysterectomy and oophorectomy;
- IUD in place for at least 3 months;
- Barrier methods with spermicide (condom, diaphragm) for at least 14 days prior to the start of the study and throughout the study;
- Surgical sterilization of the partner (vasectomy for 6 months minimum);
- Hormonal contraceptives for at least 3 months prior to the start of the study. Other birth control methods may be deemed acceptable.
- Postmenopausal women with amenorrhea for at least 2 years;
- Voluntary consent to participate in the study.
Exclusion
- Subject candidates must not be enrolled in the study if they meet any of the following criteria:
- History or presence of significant: cardiovascular, pulmonary, hepatic, renal, hematologic, gastrointestinal, endocrine, immunologic, dermatologic, neurologic or psychiatric disease.
- In addition, history or presence of:
- alcoholism or drug abuse within the past 2 years;
- hypersensitivity or idiosyncratic reaction to fenofibrate or other lipid regulating agents.
- Female subjects who are pregnant or lactating.
- Subjects who have been on an abnormal diet (for whatever reason) during the 30 days prior to the first dosing.
- Subjects who have made a donation (standard donation amount or more) of blood or blood products (with the exception of plasma as noted below) within 30 days prior to the study.
- Subjects who have made a plasma donation within 7 days prior to the study.
- Subjects who have participated in another clinical trial within 30 days prior to the first dose.
Key Trial Info
Start Date :
August 1 2002
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
October 1 2002
Estimated Enrollment :
24 Patients enrolled
Trial Details
Trial ID
NCT00775359
Start Date
August 1 2002
End Date
October 1 2002
Last Update
October 20 2008
Active Locations (1)
Enter a location and click search to find clinical trials sorted by distance.
1
MDS Pharma Services
Phoenix, Arizona, United States, 85044