CompletedPhase 3ACTRN12605000389606

IBCSG 30-04 / NCIC CTG MA.27

A randomised phase III trial of exemestane versus anastrozole in postmenopausal women with receptor positive primary breast cancer


Sponsor

Australia and New Zealand Breast Cancer Trials Group Ltd

Enrollment

5,800 participants

Start Date

Nov 10, 2005

Study Type

Interventional

Conditions

Summary

For further information, please see www.clinicaltrials.gov NCT00066573


Eligibility

Sex: FemalesMin Age: 18 Yearss

Plain Language Summary

Simplified for easier understanding

This clinical trial is studying IBCSG 30-04 / NCIC CTG MA.27. It may be open to women aged 18 and older who postmenopausal women with completely resected, histologically proven, hormone receptor-positive primary breast cancer who have a minimum life expectancy of 5 years and are accessible for follow up. Participation typically involves regular medical visits, tests, and following the study's treatment plan.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

IBCSG 30-04 / NCIC CTG MA.27 is co-ordinated by the National Cancer Institute of Canada, Clinical Trials Group (NCIC CTG). The International Breast Cancer Study Group (IBCSG) is participating in the

IBCSG 30-04 / NCIC CTG MA.27 is co-ordinated by the National Cancer Institute of Canada, Clinical Trials Group (NCIC CTG). The International Breast Cancer Study Group (IBCSG) is participating in the NCIC CTG MA.27 trial, and the ANZ Breast Cancer Trials Group (ANZ BCTG) contribution is part of the IBCSG collaboration. The trial is conducted in Australia and New Zealand by the ANZ Breast Cancer Trials Group. This study will investigate which of two drugs (exemestane and anastrozole), if either, is better at preventing a recurrence of breast cancer in postmenopausal women with receptor positive, adequately excised, primary breast cancer. IBCSG 30-04 / NCIC CTG MA.27 is an international, multicentre, randomised phase III clinical trial of 5800 postmenopausal women who have had histologically or cytologically confirmed, receptor-positive primary breast cancer. Women will be randomised in a 2-arm design to receive one of the following: a. Exemestane 25mg b. Anastrozole 1mg All treatment will be on a daily basis for 5 years until recurrence or second malignancy is documented.


Locations(1)

NSW,SA,TAS,WA,VIC, Australia

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ACTRN12605000389606