Comparative Bioavailability Study of Extended-release and Immediate-release Trazodone in Healthy Adult Volunteers

NCT ID: NCT00839072

Last Updated: 2012-04-27

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: PHASE1
• Total Enrollment: 24 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2009-02-28
• Study Completion Date: 2009-03-31

Brief Summary

The objective of the study is to compare the pharmacokinetic profiles of extended-release and immediate-release trazodone formulations

Detailed Description

The bioavailability of once-daily trazodone extended-release 300 mg caplets (test product) and trazodone immediate-release 100 mg tablets administered q8h (reference product) will be compared in healthy adult volunteers in a randomized, crossover fashion. Morning doses will be administered after an overnight fast. Blood samples will be collected predose and at pre-defined times over 72 hours following the morning dose. Pharmacokinetic parameters will be analyzed using ANOVA. Comparative bioavailability will be assessed on the basis of the ratio of least-squares means and/or 90% confidence interval criteria.

Conditions

Healthy

Study Design

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

Study Groups

Trazodone Contramid OAD

Group Type: EXPERIMENTAL

Trazodone HCl

Intervention Type: DRUG

300 mg extended-release caplet, single dose

Desyrel

Group Type: ACTIVE_COMPARATOR

Trazodone HCl

Intervention Type: DRUG

100 mg immediate-release tablet, dosing q8h

Interventions

Trazodone HCl

100 mg immediate-release tablet, dosing q8h

Intervention Type: DRUG

Trazodone HCl

300 mg extended-release caplet, single dose

Intervention Type: DRUG

Other Intervention Names

Oleptro

Eligibility Criteria

Inclusion Criteria

• Availability for entire study period and willingness to adhere to protocol requirements as evidenced by signed informed consent
• Male or female volunteer, aged between 18 and 45 years inclusively
• BMI ≥20 and <30 kg/m2
• Minimum body weight: 60 kg
• Clinical laboratory values within normal range, or without clinical significance
• Healthy according to medical history, clinical laboratory results and physical examination
• Nonsmoker or ex-smoker

Exclusion Criteria

• Significant history of hypersensitivity to trazodone or any related products, or severe hypersensitivity reactions to any drugs
• Presence or history of significant gastrointestinal, liver or kidney disease, or any other conditions known to interfere with the absorption, distribution, metabolism, or excretion of drugs or known to potentiate or predispose to undesired effects
• Presence of significant cardiovascular, pulmonary, hematologic, neurological, psychiatric, endocrine, immunologic, or dermatologic disease
• Suicidal tendency, history of or disposition to seizures, state of confusion, clinically relevant psychiatric disease
• Use of MAO inhibitors within 28 days of day 1 of the study
• Presence of significant heart disease or disorder according to ECG
• Seated systolic blood pressure lower than 90 or over 140 mmHg or diastolic blood pressure lower than 50 or over 90 mmHg at screening
• Maintenance therapy with any drug, or significant history of drug dependency or alcohol abuse (>3 units of alcohol per day, intake of excessive alcohol, acute or chronic)
• Any clinically significant illness in the previous 28 days before day 1 of this study
• Use of any enzyme-modifying drugs, including strong inhibitors of cytochrome P450 (CYP) enzymes (such as cimetidine, fluoxetine, quinidine, erythromycin, ciprofloxacin, fluconazole, ketoconazole, diltiazem, and HIV antivirals) and strong inducers of CYP enzymes (such as barbiturates, carbamazepine, glucocorticoids, phenytoin, and rifampin), in the previous 28 days before day 1 of this study
• Females who are pregnant according to a positive serum pregnancy test, or are lactating
• Females of childbearing potential who refuse to use an acceptable method of contraception from the screening visit and throughout the study
• Volunteers who took an investigational product (in another clinical trial) or donated 50 mL or more of blood in the previous 28 days before day 1 of this study
• Poor motivation, intellectual problems likely to limit the validity of consent to participate in the study or limit the ability to comply with the protocol requirements or inability to cooperate adequately, inability to understand and to observe the instructions of the physician
• Donation of 500 mL or more of blood (Canadian Blood Services, Hema-Quebec, clinical studies, etc) in the previous 56 days before day 1 of the study
• Positive urine screening for drugs of abuse
• Any history of tuberculosis and/or prophylaxis for tuberculosis
• Positive results to HIV, HBsAg, or anti-HCV tests

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

Sponsors

Algorithme Pharma Inc

INDUSTRY

Sponsor Role: collaborator

Labopharm Inc.

INDUSTRY

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Eric Sicard, MD

Role: PRINCIPAL_INVESTIGATOR

Algorithme Pharma Inc

Locations

Algorithme Pharma Inc.

Laval, Quebec, Canada

Countries

Canada

Other Identifiers

TAN-P8-681

Identifier Type: -

Identifier Source: secondary_id

04ACL1-011

Identifier Type: -

Identifier Source: org_study_id