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A total of 521 pre/postmenopausal women were randomized 2:1 to IBRANCE plus fulvestrant or placebo plus fulvestrant and stratified by documented sensitivity to prior hormonal therapy, menopausal status at study entry (pre/peri versus postmenopausal), and presence of visceral metastases

Each batch is tested for purity and identity

Possible Side Effects Injection site pain or redness Mild and temporary

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For use by qualified researchers in appropriate laboratory settings only