Anastrozole 1 mg Tablets Under Fasting Conditions

Overview

The objective of this study is to evaluate the comparative bioavailability between Anastrozole 1 mg Tablets (Teva Pharmaceuticals USA) and Arimidex® 1 mg Tablets (AstraZeneca Pharmaceuticals LP, USA), after a single-dose in healthy subjects under fasting conditions.

Full Title of Study: “A Single-Dose, Comparative Bioavailability Study of Two Formulations of Anastrozole 1 mg Tablets Under Fasting Conditions”

Study Type

  • Study Type: Interventional
  • Study Design
    • Allocation: Randomized
    • Intervention Model: Crossover Assignment
    • Masking: None (Open Label)
  • Study Primary Completion Date: September 2005

Detailed Description

Criteria for Evaluation: FDA Bioequivalence Criteria Statistical Methods: FDA Bioequivalence Statistical Methods

Interventions

  • Drug: Anastrozole (Teva Pharmaceuticals USA)
    • 1 mg Tablets
  • Drug: Anastrozole (Arimidex®)
    • 1 mg Tablets

Arms, Groups and Cohorts

  • Experimental: Investigational Test Product
    • Anastrozole Tablets, 1 mg
  • Active Comparator: Reference Listed Drug
    • Arimidex® Tablets, 1 mg

Clinical Trial Outcome Measures

Primary Measures

  • Cmax of Anastrozole(Maximum Observed Concentration of Drug Substance in Plasma)
    • Time Frame: Blood samples collected over a 72 hour period.
    • Bioequivalence based on Anastrozole Cmax.
  • AUC0-t of Anastrozole(Area Under the Concentration-time Curve From Time Zero to Time of Last Measurable Concentration)
    • Time Frame: Blood samples collected over a 72 hour period.
    • Bioequivalence based on Anastrozole AUC0-t.

Participating in This Clinical Trial

Inclusion Criteria

  • Healthy, non-smoking, post-menopausal or surgically sterile female subjects 18 years or age or older. – Body mass index (BMI) between 19 and 30, inclusive. – Indicate non-child bearing status by one of the following criteria: – Indication of successful hysterectomy. – No spontaneous menses for at least 1 year, must have luteinizing hormone (LH) and follicle stimulating hormone (FSH) levels within postmenopausal range. – Indication of successful bilateral oophorectomy. – Negative for: – HIV. – Hepatitis B surface antigen and Hepatitis C antibody. – Urine drugs of abuse test (marijuana, amphetamines, barbiturates, cocaine, opiates, benzodiazepines, and methadone). – Urine cotinine test. – Serum pregnancy test. – No significant diseases or clinically significant findings in a physical examination. – No clinically significant abnormal laboratory values. – No clinically significant findings in the 12-lead electrocardiogram (ECG). – No clinically significant findings from the vital signs measurement. – Be informed of the nature of the study and given written consent prior to receiving any study procedure. – Participants in this study will be unable to have children (i.e. post-menopausal, hysterectomy). Exclusion Criteria:

  • Known history or presence of any clinically significant medical condition. – Known or suspected carcinoma. – Known history of: – Hypersensitivity or idiosyncratic reaction to anastrozole and/or any other drug substances with similar activity. – Alcoholism within the last 12 months. – Drug dependence and/or substance abuse. – Use of tobacco or nicotine-containing products within the last 6 months. – Taken any drug known to induce or inhibit hepatic drug metabolism in the 30 days prior to dosing. – Taken any hormone replacement therapy (HRT) for 4 weeks prior to dosing. – On a special diet within 4 weeks prior to drug administration (e.g. liquid, protein, raw food diet). – Participated in another clinical trial or received an investigational product within 30 days prior to drug administration. – Donated up to 250 mL of blood within the previous 30 days OR donated from 251 to 500 mL of blood in the previous 45 days OR donated more than 500 mL of blood in the previous 56 days. – Requirement of any non-topical medication (prescription and/or over-the-counter) on a routine basis. – Difficulty fasting or consuming the standard meals. – Do not tolerate venipuncture. – Unable to read or sign the informed consent form.

Gender Eligibility: Female

Minimum Age: 18 Years

Maximum Age: N/A

Are Healthy Volunteers Accepted: Accepts Healthy Volunteers

Investigator Details

  • Lead Sponsor
    • Teva Pharmaceuticals USA
  • Overall Official(s)
    • Xueyu (Eric) Chen, M.D., Ph.D., FRCP, Principal Investigator, Pharma Medica Research, Inc.

Clinical trials entries are delivered from the US National Institutes of Health and are not reviewed separately by this site. Please see the identifier information above for retrieving further details from the government database.

At TrialBulletin.com, we keep tabs on over 200,000 clinical trials in the US and abroad, using medical data supplied directly by the US National Institutes of Health. Please see the About and Contact page for details.