Buprenorphine 8 mg Sublingual Tablets Under Fasting Conditions

NCT ID: NCT01157169

Last Updated: 2020-01-18

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: PHASE1
• Total Enrollment: 40 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2007-08-31
• Study Completion Date: 2007-09-30

Brief Summary

The object of this study is to compare the rate and extent of absorption of an investigational formulation of buprenorphine 8 mg sublingual tablets manufactured by Barr Laboratories, Inc. to an equivalent oral dose of the commercially available reference product, Subutex® manufactured by Reckitt Benckiser, following and overnight fast of at least 10 hours.

Detailed Description

Criteria for Evaluation: FDA Bioequivalence Criteria

Statistical Methods: FDA Bioequivalence Statistical Methods

Conditions

Healthy

Study Design

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

Study Groups

Investigational Test Product

Buprenorphine 8 mg Sublingual Tablets

Group Type: EXPERIMENTAL

Buprenorphine

Intervention Type: DRUG

8 mg Sublingual Tablets

Reference Listed Drug

Subutex® 8 mg Sublingual Tablets

Group Type: ACTIVE_COMPARATOR

Buprenorphine

Intervention Type: DRUG

8 mg Sublingual Tablets

Interventions

Buprenorphine

8 mg Sublingual Tablets

Intervention Type: DRUG

Buprenorphine

8 mg Sublingual Tablets

Intervention Type: DRUG

Other Intervention Names

Subutex®

Eligibility Criteria

Inclusion Criteria

• Subject must be a male or non-pregnant, non-breastfeeding female.
• Subject must be between 18 and 45 years of age (inclusive).
• Subject's Body Mass Index (BMI) must be between 18 and 30 (inclusive), and subject must weigh a minimum of 50 kg (110 lbs).
• Female subjects must agree to utilize one of the following forms of contraception from screening through 4 weeks after completion of the study. Approved forms of contraception are abstinence, double barrier, IUD in place at least 30 days prior to study drug administration, vasectomized partner, surgically sterile for at least 6 months, or at least 2 years postmenopausal.
• Subject must voluntarily consent to participate in this study and provide their written informed consent prior to completion of any study-specific procedures.
• Subject is willing and able to remain in the study unit for the entire duration of the confinement period and return for all scheduled outpatient visits.

Exclusion Criteria

• History or presence of any clinically significant cardiovascular, pulmonary, hepatic, renal, hematologic, gastrointestinal, endocrine, immunologic, dermatologic, neurologic, oncologic, or psychiatric disease or any other condition that, in the opinion of the investigator, would jeopardize the safety of the subject or the validity of the study results.
• History or presence of pancreatitis, bowel obstruction, glaucoma, enlargement of the prostate, adrenal disease, hyperthyroidism, or gallbladder disease. Subjects with a history of cholecystectomy for the treatment of gallbladder disease will be excluded.
• Females taking any oral contraceptives including estrogen and progestin combined pills, progestin-only pills, patch, or vaginal ring within 28 days prior to the first dose of study medication; using injectable contraceptives within 6 months of first dose; or who have ever had progestational hormone implants.
• Females taking hormone replacement therapy within 60 days prior to the first dose of study medication.
• Has a clinically significant abnormal finding on the physical exam, medical history, ECG, or clinical laboratory results at screening.
• History or presence of allergic or adverse response to buprenorphine, naltrexone, or any comparable or similar product.
• Has been on a significantly abnormal diet during the 4 weeks preceding the first dose of study medication.
• Has donated blood or plasma within 30 days prior to the first dose of study medication.
• Has participated in another clinical trial within 30 days prior to the first dose of study medication.
• Has used any over-the-counter (OTC) medication, including cough and cold preparations, vitamins, and herbal supplements, within 7 days prior to the first dose of study medication.
• Has used any prescription medication within 14 days prior to the first dose of study medication.
• Has consumed beverages or food containing alcohol, caffeine/xanthine, or poppy seeds from 48 hours prior to the first dose of study medication or has consumed beverages or foods containing grapefruit from 14 days prior to the first dose of study medication.
• Has been treated with any known enzyme-altering drugs, such as barbiturates, phenothiazines, cimetidine, carbamazepine, etc., within 30 days prior to the first dose of study medication.
• Has smoked or used tobacco products within 60 days prior to the first dose of study medication.
• Has a history of treatment for substance abuse (including alcohol) in the past 5 years.
• Is a female with a positive pregnancy test result.
• Has any piercing of the tongue or has a lip piercing within 30 days prior to the first dose of study medication.
• Has a positive urine screen for drugs of abuse.
• Has a positive urine alcohol test or ethanol breath test.
• Has a positive test for or has been treated for hepatitis B, hepatitis C, or HIV.

• Minimum Eligible Age: 18 Years
• Maximum Eligible Age: 45 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: Yes

Sponsors

Teva Pharmaceuticals USA

INDUSTRY

Sponsor Role: lead

Responsible Party

TEVA Pharmaceuticals, USA

Principal Investigators

Frederick A Bieberdorf, M.D., CPI

Role: PRINCIPAL_INVESTIGATOR

CEDRA Clinical Research, LLC

Locations

CEDRA Clinical Research, LLC

Austin, Texas, United States

Countries

United States

Other Identifiers

20-A63-AU

Identifier Type: -

Identifier Source: org_study_id