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Bioequivalence Study of Fenofibrate Capsules, 130 mg Under Fed Conditions

Information source: Ranbaxy Inc.
ClinicalTrials.gov processed this data on August 23, 2015
Link to the current ClinicalTrials.gov record.

Condition(s) targeted: Healthy

Intervention: fenofibrate (Drug); ANTARA® (fenofibrate) (Drug)

Phase: N/A

Status: Completed

Sponsored by: Ranbaxy Laboratories Limited

Summary

The study was conducted as an open-label, balanced, randomized, two-treatment, two-period, two-sequence, single-dose, crossover, bioequivalence study comparing Fenofibrate capsules, USP 130 mg manufactured by Ohm Laboratories Inc, NJ 08901 with ANTARA® (fenofibrate) capsules 130 mg manufactured by Ethypharm Industries Saint Cloud, France for Oscient Pharmaceuticals Corp. Waltham, MA 02451 in healthy, adult, male, human subjects under fed condition.

Clinical Details

Official title: An Open Label, Balanced, Randomized, Two-treatment, Two-period, Two-sequence, Single Dose, Crossover Bioequivalence Study Comparing Fenofibrate Capsule 130 mg of Ohm Laboratories Inc., USA (A Subsidiary of Ranbaxy Pharmaceuticals Inc., USA) With Antara® Capsule 130 mg (Containing Fenofibrate 130 mg) of Oscient Pharmaceutical Corporation, USA in Healthy, Adult, Male Human Subjects Under Fed Conditions

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

Primary outcome:

Area under the plasma concentration versus time curve (AUC) of fenofibric acid

Peak Plasma Concentration (Cmax) of fenofibric acid

Detailed description: The subjects were subjected to breath test for alcohol and test for drugs of abuse (opioids and cannabinoids) in urine prior to admission in each period. Following an overnight fast of at least 10 hour, a high-fat high calorie breakfast was served to the study subjects. Thirty minutes after start of this breakfast, a single oral dose of fenofibrate capsules 130 mg of either test or reference formulation was administered during each period of the study, along with 240 mL of drinking water at ambient temperature under low light condition and under supervision of trained study personnel. Blood samples were collected at pre-dose and at 1. 000, 2. 000, 3. 000, 4. 000, 4. 500, 5. 000, 5. 500, 6. 000, 6. 500, 7. 000, 7. 500, 8. 000, 8. 500, 9. 000, 9. 500, 10. 000, 11. 000, 12. 000, 16. 000, 24. 000, 36. 000, 48. 000, 72. 000 and 96. 000 hours post dose in each period under low light condition. The pre-dose blood samples in each period were collected in duplicate (2 x 5 mL), within a period of 1. 5 hour before dosing. Post-dose samples were generally collected within 2 minutes of the scheduled time. During the course of the study, safety parameters assessed were vital signs, clinical examination, medical history and clinical laboratory safety tests (hematology, biochemical parameters, serology and urine analysis at screening). Adverse event monitoring was done throughout the study. Laboratory parameters of hematology and biochemistry were repeated at the end of the study.

Eligibility

Minimum age: 18 Years. Maximum age: 45 Years. Gender(s): Male.

Criteria:

Inclusion Criteria: Volunteers who met the following criteria were included in the study

- Were in the age range of 18-45 years.

- Were neither overweight nor underweight for his height as per the Life Insurance

- Corporation of India height/weight chart for non-medical cases.

- Had voluntarily given written informed consent to participate in this study.

- Were of normal health as determined by medical history and physical examination of

the subjects performed within 21 days prior to the commencement of the study.

- Had a non-vegetarian dietary habit.

Exclusion Criteria:

- Subject had history of hypersensitivity to fenofibrate or any related drug or to any

other drug.

- Subjects with history of hepatic or severe renal dysfunction, including primary

biliary cirrhosis.

- Subjects with history of unexplained persistent liver function abnormality.

- Subjects with history of preexisting gallbladder disease.

- Subject had history of myalgia, muscle tenderness or weakness or myopathy

- Subject had any evidence of organ dysfunction or any clinically significant deviation

from the normal in physical or clinical determinations.

- Clinically abnormal ECG or Chest X-ray, or hematological and biochemical parameters

which was/were outside acceptable limits and was judged clinically significant by investigator.

- Investigations with blood samples of the subject showed presence of disease markers

of HIV 1 or 2, Hepatitis B or C Viruses of syphilis infection.

- Investigations with urine samples of the subject showed clinically abnormal chemical

and microscopic examination of urine defined as presence of RBC, WBC (>4 /HPF), glucose (Positive) or Protein (Positive).

- Subject had history of serious medical illnesses including but not limited to

gastrointestinal, hepatic, renal, cardiovascular, pulmonary, neurological or hematological disease, diabetes, glaucoma, any serious, potentially life-threatening illness.

- Inability to communicate well (i. e. language problem, poor mental development,

psychiatric illness or poor cerebral function) that might impair the ability to provide, written informed consent.

- Subject was a regular smoker, who smoked 10 or more cigarettes daily or had

difficulty abstaining from smoking for the duration of each study period.

- Subject had history of drug dependence or excessive alcohol intake on a habitual

basis or has difficulty in abstaining for the duration of each study period.

- Use of any regular medication (OTC or prescription) or any drug metabolizing enzyme

within 30 days prior to Day 1 of this study.

- Subject had participated in a clinical trial within 12 weeks preceding admission of

this study (except for the subjects who dropout/withdrawn from the previous study prior to period I dosing).

- Subject had donated and/or lost more than 350 mL of blood in the past 3 months,

including blood loss in this study.

- Consumption of alcohol for 48 hours prior to admission.

- Consumption of grapefruit juice and or grape fruit supplements containing products

for 48 hours prior to admission.

- Subject had problem(s) in complying with the study protocol.

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Starting date: October 2009
Last updated: December 1, 2014

Page last updated: August 23, 2015

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