Phase 3 Trial of Elacestrant Versus Standard of Care for the Treatment of ER+/HER2- Advanced Breast Cancer

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• Critical Inclusion Criteria:
• Participants with proven diagnosis of adenocarcinoma of the breast with evidence of either locally advanced disease not amenable to resection or radiation therapy with curative intent or metastatic disease not amenable to curative therapy.
• Participants must be appropriate candidates for endocrine monotherapy
• Participants must have measurable disease or bone only disease with evaluable lesions
• Female or male participants age ≥ 18 years; female participants must be postmenopausal women, and male participants must not allow pregnancy with their sperm (abstain, do not donate sperm, et cetera).
• Participants must have ER+ and HER2- tumor status
• Participants must have previously received at least one and no more than two lines of endocrine therapy for advanced/metastatic breast cancer and meet additional previous treatment criteria.
• Participants must have received prior treatment with a CDK4/6 inhibitor in combination with either fulvestrant or an aromatase inhibitor (AI) for advanced/metastatic breast cancer (mBC).
• Participants may have received no more than one line of chemotherapy in the advanced/metastatic setting.
  • Critical Exclusion Criteria:
• Prior treatment with elacestrant or other investigational selective estrogen receptor degrader (SERD) or ER antagonist (D-0502, GDC-0810, GDC-0927, GDC-9545, G1T-48, LSZ102, AZD9496, SAR439859, ZN-c5, H3B-6545, bazedoxifene, lasofoxifene).
• Prior anticancer or investigational drug treatment within the following windows:
  • Fulvestrant treatment < 42 days before first dose of study drug
  • Any endocrine therapy < 14 days before first dose of study drug
  • Chemotherapy < 21 days before first dose of study drug
  • Any investigational anti-cancer drug therapy < 28 days or five half-lives (whichever is shorter) before the first dose of study drug. Enrollment of participants whose most recent therapy was an investigational agent should be discussed with the Sponsor
  • Bisphosphonates or RANKL inhibitors initiated or dose changed < 3 months prior to first dose of study drug
• Presence of symptomatic visceral disease as defined in protocol.