The purpose of the study is to assess the efficacy and safety of the addition of Tersolisib (LY4064809/STX-478) to other anti-cancer drugs as first treatment for advanced hormone receptor-positive (HR+)/human epidermal growth factor receptor 2-negative (HER2-) breast cancer. Participants can remain in the study as long as the drug is helping the cancer without unbearable side effects.
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(Part 1): Overall Response Rate (ORR): Percentage of Participants with Confirmed Complete Response (CR) or Partial Response (PR)
Timeframe: Baseline through disease progression or death (Estimated up to 5 years)
(Part 2): Progression-Free Survival
Timeframe: Baseline to objective progression or death due to any cause (Estimated up to 5 years)
Trial questions or participation questions: 1-877-CTLILLY (1-877-285-4559) or