ITA - Clinical Study Comparing ARIMIDEX™ With NOLVADEX™ in Women With Breast Cancer Treated With NOLVADEX for at Least 2 Years

NCT00286117 · Status: COMPLETED · Phase: PHASE3 · Type: INTERVENTIONAL · Enrollment: 448

Last updated 2009-05-01

No results posted yet for this study

Summary

The purpose of this study was to assess the difference in disease-free survival between post-menopausal women with hormone receptor-positive early breast cancer who switched from tamoxifen to anastrozole and those who continued on tamoxifen.

Conditions

Interventions

DRUG

Anastrozole

oral

DRUG

Tamoxifen

oral

Sponsors & Collaborators

  • Institute of Cancer Research, United Kingdom

    collaborator OTHER
  • AstraZeneca

    lead INDUSTRY

Principal Investigators

  • AstraZeneca Arimidex Medical Science Director, MD · AstraZeneca

  • Francesco Boccardo, MD · University and National Cancer Research Institute

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
PARALLEL

Eligibility

Max Age
75 Years
Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
1998-03-31
Completion
2006-05-31

Countries

  • Italy

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT00286117 on ClinicalTrials.gov