Bioequivalency Study of Divalproex Sodium DR Tablets, 500 mg of Dr.Reddy's Under Fasting Conditions

The purpose of this study is to assess the bioavailability of Divalproex Sodium DR Tablets 500 mg versus Depakote DR 500 mg tablets with a washout period of 10 days in healthy subjects.

An open label, balanced, randomized, two-treatment, two-period, two-sequence, single dose, crossover, bioequivalence study of Divalproex sodium DR 500 mg tablets of Dr.Reddy's Laboratories Limited, Generics, India comparing with that of Depakote® DR (containing Divalproex sodium) 500 mg tablets of Abbott Laboratories PR Ltd., Barceloneta, PR, in healthy, adult, human subjects under fasting conditions.

• Experimental: Divalproex Sodium DR Tablets 500 mg
  Divalproex Sodium DR Tablets 500 mg of Dr. Reddy's Laboratories Limited
  Intervention: Drug: Divalproex Sodium
• Active Comparator: Depakote DR 500 mg Tablets
  Depakote DR 500 mg Tablets of Abbott Laboratories PR Ltd.,
  Intervention: Drug: Divalproex Sodium

Inclusion Criteria:

Subjects must fulfill all of the following criteria to be considered for inclusion into this study:

• Subjects who will provide written informed consent.
• Subjects must be healthy, adult, human beings within 18-45 years of age (both inclusive)weighing at least 50 kg.
• Having a Body Mass Index (BMI) between 18.5 and 24.9 (both inclusive), calculated as weight in Kg/height in m2
• Subjects must be of normal health as determined by medical history and physical examination performed within 21 days prior to the commencement of the study.
• Subjects whose screening laboratory values are within normal limits or considered by the physician/investigator to be of no clinical significance.
• Availability of the subject for the entire study period and willingness to adhere to the protocol requirements as evidenced by written informed consent.

Exclusion Criteria:

The subjects will be excluded based on the following criteria during screening and during the study

• Subjects incapable of understanding the informed consent.

• Subjects who have:

  • Systolic blood pressure less than 90 mm of Hg and more than 140 mm of Hg
  • Diastolic blood pressure less than 60 mm of Hg and more than 94 mm of Hg. Minor deviations (2-4 mm of Hg) at check-in may be acceptable at the discretion of the physician/investigator.
  • Pulse rate below 50/min and above 100/min.
• History of hypersensitivity or idiosyncratic reaction to Divalproex sodium or any other related drugs.
• Any evidence of impairment of renal, hepatic, cardiac, lung or gastrointestinal function.
• Consumption of grapefruit for the past ten days prior to the dosing day until the completion of the study.
• Regular smoker who has a habit of smoking more than nine cigarettes per day and has difficulty in abstaining from smoking from 48 hours before dosing and during sampling period
• Subjects who have taken over the counter or prescribed medications and enzyme modifying or any systemic medication for during the last 7 and 30 days respectively before dosing.
• Subjects who have participated in any other clinical investigation using experimental drug/donated blood in past 90 days before the date of start of study.
• Subjects with clinically significant abnormalities (such as Laboratory Findings, ECG, X-Ray,Drugs of abuse, Alcohol etc.,) and/or with significant diseases (such as HIV, HCV, Syphilis,Hepatitis B etc.,).
• Female subjects who are pregnant or who are able (women with child bearing potential) to become pregnant during the study.