Bioequivalence Study for Lamotrigine Tablets 200 mg Under Fasting Condition

NCT ID: NCT01513720

Last Updated: 2012-01-20

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: PHASE1
• Total Enrollment: 20 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2002-12-31
• Study Completion Date: 2002-12-31

Brief Summary

This is an single dose,two-way, crossover, oral bioequivalence study.

Detailed Description

The study was an single dose, two-way crossover, oral bioequivalence study of Lamotrigine tablets 200 mg of Dr. Reddy's Laboratories Limited, India comparing with that of LAMICTAL® tablets 200 mg of GlaxoSmithKline Inc, in healthy, adult, human subjects under fasting condition. 26 subjects (19 men and 7 womens) are enrolled and completed the study. The washout period is 14 days between the two periods of the study.

Conditions

Healthy

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: CROSSOVER
• Primary Study Purpose: TREATMENT
• Blinding Strategy: NONE

Study Groups

Lamotrigine Tablets 200 mg

Lamotrigine Tablets 200 mg of Dr. Reddy's Laboratories Limited

Group Type: EXPERIMENTAL

Lamotrigine

Intervention Type: DRUG

Lamotrigine Tablets 200 mg

Lamictal®

Intervention Type: DRUG

Lamictal® 200 mg Tablets

Lamictal® 200 mg Tablets

Lamictal® 200 mg Tablets of GlaxoSmithKline Inc

Group Type: ACTIVE_COMPARATOR

Lamotrigine

Intervention Type: DRUG

Lamotrigine Tablets 200 mg

Lamictal®

Intervention Type: DRUG

Lamictal® 200 mg Tablets

Interventions

Lamotrigine

Lamotrigine Tablets 200 mg

Intervention Type: DRUG

Lamictal®

Lamictal® 200 mg Tablets

Intervention Type: DRUG

Other Intervention Names

Lamictal® 200 mg

Eligibility Criteria

Inclusion Criteria

1. Healthy males and females at least 18 years of age inclusive

2. Informed of the nature of the study and given written informed consent

3. Have a body weight within 15% of the appropriate range as defined in the 1983 Metropolitan Life Company tables and weighing at least 100 lbs.

Exclusion Criteria

1. Hypersensitivity to Lamotrigine (Lamictal®) or similar compounds

2. Any history of a clinical condition which might affect drug absorption, metabolism or excretion

3. Recent history of mental illness, drug addition,drug abuse or alcoholism

4. Donation of greater than 500 ml of blood in the past 4 weeks prior to study dosing of difficulty in donating blood.

5. Received an investigational drug within the 4 weeks prior to study dosing.

6. Currently taking any prescription medication, except oral contraceptives, within the 7 days prior to study dosing or over-the -counter medication within 3 days of study dosing. This prohibition does not include vitamins or herbal preparations taken as nutritional supplements for non-therapeutics indications as judged by the attending physician.

7. Tobacco use (>5 cigarettes per day) in the 3 months prior to study dosing.

8. If female, the subjects is lactating or has a positive pregnancy test screening and prior to each of the two treatments periods. Females of child bearing potential must use a medical acceptable method of contraception throughout the entire study period and for one week after the study is completed. Medically acceptable methods or contraception that may be used by the subject and/or her partner are; oral contraceptives, progestin injection or implants, condom with spermicide, diaphragm with spermicide, IUD, vaginal spermicidal suppository, surgical sterilization of their partner(s) or abstinence. Females taking oral contraceptives must have taken them consistently for at least three months prior to receiving study medication.

• Minimum Eligible Age: 20 Years
• Maximum Eligible Age: 44 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: Yes

Sponsors

Dr. Reddy's Laboratories Limited

INDUSTRY

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Dr. Ralph Scallion, MD

Role: PRINCIPAL_INVESTIGATOR

AAI Clinic

Locations

AAI Clinic

Quadrangle Drive, North Carolina, United States

Countries

United States

Other Identifiers

AAI-US-137

Identifier Type: -

Identifier Source: org_study_id