Bioequivalence Study of Mycophenolate Mofetil 250 mg Capsule, Under Fed Conditions

• Status: Completed
• Trial end date: 2009-02-01
• Target enrollment: 0
• Participant gender: All

Summary

An open-label, balanced, randomized, two-treatment, two-period, two sequence, single dose, crossover, bioequivalence study of Mycophenolate mofetil 250 mg Capsule of Dr. Reddy's Laboratories limited, comparing with that of Cellcept 250 mg Capsule of Roche Laboratories in healthy, adult, human, male subjects under fed conditions.

• Phase: Phase 1
• Accepts Healthy Volunteers?: Accepts Healthy Volunteers

Details

• Lead Sponsor: Dr. Reddy's Laboratories Limited
• Treatments: Mycophenolate mofetil; Mycophenolic Acid

Criteria

Inclusion Criteria:

• Healthy, adult, human male volunteers between 18 - 55 years of age (both inclusive) living in and around Ahmedabad city of western part of India.

• Having a Body Mass Index (BMI) between 18.5 - 24.9 (both inclusive), calculated as weight in kg/height in meter2.

• Have no significant diseases or clinically significant abnormal findings during screening, medical history, physical examination, laboratory evaluations, 12- lead ECG and X-ray chest recordings.

• Able to comply with the study procedures, in the opinion of the Principal investigator.

• Able to give voluntary written informed consent for participation in the study.

Exclusion Criteria:

• Known hypersensitivity or idiosyncratic reaction to Mycophenolate mofetil or any related drug.

• Any disease or condition that compromised the haemopoietic, renal, hepatic, endocrine, pulmonary, central nervous, cardiovascular, immunological, dermatological, gastrointestinal or any other body system.

• Ingestion of a medicine at any time with in 14 days before dosing in Period-I. In any such case subject selection was at the discretion of the Principal Investigator.

• Any history or presence of asthma (including aspirin induced asthma) or nasal polyp or NSAID induced urticaria.

• A recent history of alcoholism (< 2 years) or of moderate (180 mL/day) alcohol use, or consumption of alcohol within 48 hours prior to receiving study medicine.

• Smokers, who smoked 10 or more than 10 cigarettes/day or inability to abstain from smoking during the study.

• Consumption of Grapefruits or its products within a period of 48 hours prior to dosing.

• The presence of clinically significant abnormal laboratory values during screening.

• Use of any recreational drugs or history of drug addiction or testing positive in pre-study drug scans.

• History of psychiatric disorders.

• A history of difficulty with donating blood.

• Donation of blood (1 unit or 350 mL) or receipt of an investigational product or participation in a drug research study within a period of 90 days prior to the first dose of study medicine. Elimination half-life of the study drug was taken into consideration for inclusion of the subject in the study.

Note: If subject had participated in a study in which blood loss was ≤ 200 mL, subject could be enrolled 60 days after the last sample of previous study.

• A positive hepatitis screen including hepatitis B surface antigen and HCV antibodies.

• A positive test result for HIV antibody and/or syphilis.

• An unusual diet, for whatever reason (e.g. low-sodium), for four weeks prior to receiving the study medicine and throughout the subjects' participation in the study. In any such case subject selection was at the discretion of the Principal Investigator.

All the enrolled subjects satisfied all the above inclusion and exclusion criteria.