Bioequivalency Study of Anastrozole 1 mg Under Fasted Conditions

N/ACompletedNCT01155102

Roxane Laboratories31 enrolled

Overview

The objective of this study was to prove the bioequivalence of Anastrozole Tablet under fasted conditions.

Study Type

INTERVENTIONAL

Allocation

RANDOMIZED

Purpose

TREATMENT

Masking

NONE

Enrollment

Conditions

Breast Cancer

Interventions

AnastrozoleDRUG

1 mg tablet

Eligibility

Sex: ALLMin age: 18 YearsMax age: 45 YearsHealthy volunteers:

Medical Language ↔ Plain English

Inclusion Criteria: * No clinically significant abnormal findings on the physical examination, medical history, or clinical laboratory results during screening Exclusion Criteria: * Positive test for HIV, Hepatitis B, or Hepatitis C. * Treatment with known enzyme altering drugs. * History of allergic or adverse response to anastrozole or any comparable or similar product.

Locations (1)

Bio-Kinetic Clinical Applications

Springfield, Missouri, United States

Outcomes

Primary Outcomes

bioequivalence determined by statistical comparison Cmax

Time frame: 31 days

Data from ClinicalTrials.gov

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