Skip to content
Trial Eligibility
Menu

A Study of Imlunestrant (LY3484356) in Premenopausal Women With Estrogen Receptor-Positive (ER+) Human Epidermal Growth Factor Receptor 2 Negative (HER2-) Early Breast Cancer

NCT07287098

This study is recruiting at 6 US sites in 5 states, according to its ClinicalTrials.gov record last updated .

Summary

This study will include two groups of patients: Cohort 1 and Cohort 2. Cohort 1: will help researchers learn how a medicine called imlunestrant (LY3484356) affects a specific type of breast cancer. Some patients will take both imlunestrant and another treatment to suppress their ovarian function. Some will take it without ovarian suppression. Researchers will compare the effects in breast cancer cells to those of another medicine called tamoxifen. All patients in this group will be premenopausal women who have a type of early breast cancer called estrogen receptor-positive, HER2-negative.

Shortened from the sponsor's brief summary. View official record on ClinicalTrials.gov

Conditions studied

  • Breast Neoplasms

Eligibility basics and study details

Study type
Interventional
Phase
Phase 2
Ages
18 years and older
Sex
Female
Healthy volunteers
Not accepted
Sponsor
Eli Lilly and Company
Last updated on ClinicalTrials.gov
October 8, 2026

These are the basic criteria only. The full inclusion and exclusion criteria are on the official record, and the study team decides who can take part.

US recruiting sites

Indiana · 1

  • Indiana University Melvin and Bren Simon Cancer Center · Indianapolis, IN

New York · 1

  • New York Cancer and Blood Specialists · Shirley, NY

Tennessee · 1

  • Tennessee Oncology · Nashville, TN

Texas · 2

  • Oncology Consultants P.A. · Houston, TX
  • University of Texas MD Anderson Cancer Center · Houston, TX

Virginia · 1

  • Inova Schar Cancer Institute · Fairfax, VA

Source: ClinicalTrials.gov, data processed . Recruiting US sites filtered by distance and site status; summaries shortened.