Expired Study
This study is not currently recruiting Study Participants on ClinicalConnection.com. If you would like to find active studies please search for clinical trials.

Morgantown, West Virginia 26505


Purpose:

The objective of this study was to investigate the bioequivalence of Mylan's divalproex sodium-delayed-release tablets 500 mg tablets to Abbott's Depakote® 500 mg tablets following a single, oral 500 mg (1 x 500 mg) dose administration under fasting conditions.


Criteria:

Inclusion Criteria: 1. Age: 18 years and older. 2. Sex: Females not of child bearing potential and males. - No hormonal contraceptives or hormonal replacement therapies are permitted in this study. - Women will not be considered of childbearing potential if one of the following is reported and documented on the medical history: - postmenopausal with spontaneous amenorrhea for at least one (1) year, or spontaneous amenorrhea for less than one (1) year with serum FSH levels > 40 mIU/ml, or - bilateral oophorectomy with or without a hysterectomy and an absence of bleeding for at least 6 months, or - total hysterectomy and an absence of bleeding for at least 3 months. - During the course of the study, from study screen until study exit - including the washout period, all men must use a spermicide containing barrier method of contraception in addition to their current contraceptive method. These instructions should be documented in the informed consent form. 3. Weight Restrictions: - At least 60 kg (132 lbs) for men and - At least 48 kg (106 lbs) for women - All subjects will have a Body Mass Index (BMI) less than or equal to 30 but greater than or equal to 19 (see Part II, Administrative Aspects of Bioequivalence Protocols). BMI values should be rounded to the nearest integer (ex. 30.4 rounds down to 30, while 18.5 rounds up to 19) 4. All subjects should be judged by the principal or sub-investigator physician listed on the Form FDA 1572 as normal and healthy during a pre-study medical evaluation performed within 21 days of the initial dose of study medication which will include: 5. Normal or non-clinically significant physical examination including vital signs, 6. Within normal limits or non-clinically significant laboratory evaluation results for the following tests: - Serum Chemistries: sodium, potassium, chloride, BUN, iron, albumin, total protein AST, Alk. Phos., Calcium, Creatinine, ALT, Total bilirubin, Total Cholesterol, Phosphate, Uric Acid, Non-fasting Glucose Triglycerides - Hematology: Platelet Count, Hemoglobin, Leukocyte Differential, Hematocrit, Red Blood Cells - Urinalysis: Appearance, Specific Gravity, Protein pH, Microscopic Examination 7. Negative Hepatitis B and Hepatitis C tests, 8. Negative HIV test, 9. Normal or non-clinically significant 12-lead ECG 10. Negative urine drug screen for all of the following compounds: amphetamines, barbiturates, benzodiazepines, cannabinoid, cocaine, methadone, opiates, and phencyclidine Exclusion Criteria: 1. Institutionalized subjects will not be used. 2. Social Habits: - Use of any tobacco-containing products within 1 year of the start of the study. - Ingestion of any alcoholic, caffeine- or xanthine-containing food or beverage within the 48 hours prior to the initial dose of study medication. - Ingestion of any vitamins or herbal products within 7 days prior to the initial dose of the study medication. - Any recent, significant change in dietary or exercise habits. - Individual has a history of drug and/or alcohol abuse. 3. Medications: - Use of any prescription or over-the-counter (OTC) medications within fourteen (14) days prior to the initial dose of study medication. - Use of any hormone replacement therapy within 3 months prior to study medication dosing. - Use of any medication known to induce or inhibit hepatic enzyme activity within 28 days prior to the initial dose of study medication (see Part II, Administrative Aspects of Bioequivalence Protocols for list). 4. Diseases: - History of any significant cardiovascular, hepatic, renal, pulmonary, hematologic, gastrointestinal, endocrine, immunologic, dermatologic, congenital metabolic disorders or neurologic disease. - Acute illness at the time of either the pre-study medical evaluation or dosing. - All laboratory values reflecting hepatic function must be with in 10% of the upper range of normal in order to be considered not clinically significant. 5. Subjects who have known urea cycle disorders which are a group of uncommon genetic abnormalities (e.g. ornithine transcarbamylase deficiency). 6. Donation or loss of a significant volume of blood or plasma (> 450 mL) within 28 days prior to the initial dose of study medication. 7. Subjects who have received an investigational drug within 30 days prior to the initial dose of study medication. 8. Allergy or hypersensitivity to Divalproex Sodium or any related products. 9. History of difficulties in swallowing, or any gastrointestinal disease which could affect the drug absorption. 10. Consumption of grapefruit or grapefruit containing products within 7 days of drug administration


Study is Available At:


Original ID:

DIVA-0771


NCT ID:

NCT01184391


Secondary ID:


Study Acronym:


Brief Title:

Bioequivalence Study of Divalproex Sodium Delayed-Release Tablets, 500 mg


Official Title:

Single-Dose Fasting Bioequivalence Study of Divalproex Sodium Delayed-Release Tablets (500 mg; Mylan) and Depakote Tablets (500 mg; Abbott) in Healthy Adult Male And Female (Not of Childbearing Potential) Volunteers


Overall Status:

Completed


Study Phase:

Phase 1


Genders:

Both


Minimum Age:

18 Years


Maximum Age:

N/A


Quick Facts

Healthy Volunteers
Oversight Has DMC
Study Is FDA Regulated
Study Is Section 801
Has Expanded Access

Study Source:

Mylan Pharmaceuticals


Oversight Authority:

United States: Institutional Review Board


Reasons Why Stopped:


Study Type:

Interventional


Study Design:

Allocation: Randomized, Endpoint Classification:


Number of Arms:

2


Number of Groups:

0


Total Enrollment:

17


Enrollment Type:

Actual


Study Dates

Start Date:July 2007
Completion Date:August 2007
Completion Type:Actual
Primary Completion Date:August 2007
Primary Completion Type:Actual
Verification Date:August 2010
Last Changed Date:August 17, 2010
First Received Date:September 24, 2009

Study Outcomes

Outcome Type:Primary Outcome
Measure:AUCI
Time Frame:30 days
Safety Issues:False
Description:Area under the concentration time curve from time zero to infinity (micrograms x mL/hr)
Outcome Type:Primary Outcome
Measure:AUCL
Time Frame:30 days
Safety Issues:False
Description:Area under the concentration time curve from time zero to the last measurable concentration(micrograms x mL/hr)
Outcome Type:Primary Outcome
Measure:Cmax
Time Frame:30 days
Safety Issues:False
Description:Maximum plasma concentration (micrograms/mL)

Study Interventions

Intervention Type:Drug
Name:DIVALPROEX SODIUM DELAYED-RELEASE TABLETS, USP, 50
Description:1 X 500 mg Tablet, under fasting conditions.
Arm Name:Test: Divalproex Sodium
Intervention Type:Drug
Name:DEPAKOTE® Tablets, 500 MG
Description:1 x 500 mg tablet, under fasting conditions
Arm Name:Reference: Depakote Tablets

Study Arms

Study Arm Type:Experimental
Arm Name:Test: Divalproex Sodium
Description:DIVALPROEX SODIUM DELAYED-RELEASE TABLETS, USP, 500 MG
Study Arm Type:Active Comparator
Arm Name:Reference: Depakote Tablets
Description:DEPAKOTE® Tablets, 500 MG Abbott Laboratories

Study Agencies

Agency Class:Industry
Agency Type:Lead Sponsor
Agency Name:Mylan Pharmaceuticals

Sample and Retention Information

There are no available Sample and Retention Information

Study References

There are no available Study References

Data Source: ClinicalTrials.gov

Date Processed: October 09, 2019

Modifications to this listing: Only selected fields are shown, please use the link below to view all information about this clinical trial.


This study is not currently recruiting Study Participants. The form below is not enabled.