A Relative Bioavailability Study of Sertraline HCl 100 mg Tablets Under Non-fasting Conditions

Completed · Phase 1

Conditions studied: Healthy

In brief

To compare the rate of absorption and oral bioavailability of a test formulation of Sertraline 100 mg tablets manufactured by Purepac Pharmaceutical Company to an equivalent oral dose of the commercially available reference product, Zoloft® manufactured by Pfizer Inc. Following an overnight fast of at least 10 hours, subjects will consume a standard high-calorie, high-fat breakfast meal. This standard breakfast will begin 30 minutes prior to each dose.

Key facts

Study ID: NCT00864019
Run by: Actavis Inc.
People needed: 30
Starts: 2004-08-01
Expected to finish: 2004-08-01
Last updated by the study team: 2010-08-16

Who can join

Age: 18 and older, up to 55. Sex: any. Healthy volunteers: accepted.

You may qualify if…

Subject must be a male or non-pregnant, non-breast-feeding female.
Subject must be between 18 and 55 years of age inclusive.
Subject's body weight should be within ±15% of the ideal body weight for their height and estimated frame based on the Metropolitan Life Insurance Company Table.
Female subjects --- not surgically sterile or at least two years postmenopausal --- must agree to utilize one of the following forms of contraception, if sexually active with a male partner, from screening through completion of the study. Approved forms of contraception are abstinence, hormonal (oral, implant, transdermal or injection), double barrier (condom and diaphragm with spermicide), IUD, or vasectomized partner (6 months minimum).
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 each confinement period and return to the study site for all out-patient visits.

You may not qualify if…

History or presence of clinically significant cardiovascular, pulmonary, hepatic, renal, hematologic, gastrointestinal, endocrine, immunologic, dermatologic, neurologic, oncologic or psychiatric disease or any other condition which, in the opinion of the Investigator would jeopardize the safety of the subject or the validity of the study results.
Has a clinically significant abnormal finding on the physical exam, medical history or clinical laboratory results at screening.
History or presence of allergic or adverse response to the study drug or related drugs.
Has been on a significantly abnormal diet during the four 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 first dose of study medication.
Has used any over-the-counter (OTC) medication including vitamins, within 7 days prior to the first dose of study medication.
Has used any prescription medication, except hormonal contraceptive or hormonal replacement therapy, within 7 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.
Female with a positive pregnancy test.
Positive urine screen for drugs of abuse (amphetamines, barbiturates, benzodiazepines, cocaine, cannabinoids, opiates).
Has had a positive test for, or has been treated for hepatitis B, hepatitis C or HIV.

Where it is running

CEDRA Clinical Research, LLC — Austin, Texas, United States

Full record on ClinicalTrials.gov

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