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

• Status: Completed
• Trial end date: 2009-01-01
• 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 fasting 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:

• Subjects aged between 18 and 50 years (including both).

• Subjects' weight within the normal range according to normal values for the Body

• Mass Index (1 8.5 to 24.9 kg/m2) with minimum of 50 kg weight.

• Subjects with clinically acceptable normal health as determined by personal medical history, clinical examination and laboratory examinations within the clinically acceptable reference range.

• Subjects having clinically acceptable 12-lead electrocardiogram (ECG).

• Subjects having clinically acceptable chest X-Ray (PIA view).

• Subjects having negative urine screen for drugs of abuse (including amphetamines, barbiturates, benzodiazepines, marijuana, cocaine, and morphine).

• Subjects having negative alcohol breath test.

• Subjects willing to adhere to the protocol requirements and to provide written informed consent.

Exclusion Criteria:

The subjects were excluded from the study, if they meet any of the following criteria:

• Hypersensitivity to Mycophenolate Mofetil or related drugs.

• History or presence of significant cardiovascular, pulmonary, hepatic, renal, gastrointestinal, endocrine, immunological, dermatological, neurological or psychiatric disease or disorder.

• History or presence of significant alcoholism or drug abuse in the past one year.

• History or presence of significant smoking (more than 10 cigarettes day or consumption of tobacco products).

• History or presence of asthma, urticaria or other significant allergic reactions.

• History or presence of significant gastric and/or duodenal ulceration.

• History or presence of glaucoma, prostatic hypertrophy or obstruction of the bladder neck, cardio-spasm and myasthenia gravis.

• History or presence of significant thyroid disease, adrenal dysfunction, organic intracranial lesion such as pituitary tumor.

• History or presence of cancer.

• Difficulty with donating blood.

• Difficulty in swallowing solids like tablets or capsules.

• Use of any prescribed medication or OTC medicinal products during the last two week prior to initiation of study.

• Major illness during 3 months before screening.

• Participation in a drug research study within past 3 months.

• Donation of blood in the past 3 months before screening.

• Positive screening test for any one or more: HIV, Hepatitis B and Hepatitis C.

• History or presence of significant easy bruising or bleeding.

• History or presence of significant recent trauma.