Regulatory approval

Published by the Health Products Regulatory Authority. Approved

Aromasin is indicated for the adjuvant treatment of postmenopausal women with oestrogen receptor positive invasive early breast cancer (EBC), following 2 - 3 years of initial adjuvant tamoxifen therapy.

This is written in the approval document.

Citation

Pfizer Healthcare Ireland. Aromasin 25 mg coated tablets (Exemestane) [summary of product characteristics]. Health Products Regulatory Authority website. https://assets.hpra.ie/products/Human/23117/Licence_PA0822-111-001_09012025155108.pdf. Revised January 2025. Accessed May 25, 2025.

Therapeutic response

Precision oncology relationships for therapeutic response derived from this regulatory approval.

Organizations	Biomarkers	Cancer types	Therapies
HPRA (1)	ER positive	Invasive Breast Carcinoma	Exemestane

Contributions

Date	Contributor	Description
2024-11-10	Van Allen lab	Adding HRPA approvals for use to database