Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

NCT07287098 · ClinicalTrials.gov registry record · Phase 2

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

A Phase 2 study, sponsored by Eli Lilly and Company.

Recruiting
Registry status
Phase 2
Development phase
600
Enrollment target

NCT07287098: Recruiting Phase 2 study, sponsored by Eli Lilly and Company.

NCT07287098 is a Phase 2 study that is actively recruiting participants, run by Eli Lilly and Company. The registered enrollment target is 600 participants, above the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (351% higher). According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT07287098, a Phase 2 study, is actively recruiting participants, sponsored by Eli Lilly and Company.

RECRUITING
Registry status
Phase 2
Development phase
600 participants
Enrollment target

Study 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. The treatment in this group will last for up to 29 days. Cohort 2: will help researchers understand how imlunestrant affects the ovaries when it is taken without ovarian suppression. Researchers will compare the effects to those of another medicine called tamoxifen. This group will also include premenopausal women with the same type of breast cancer. The treatment in this group will last for up to 6 months.

Interventions

  • DRUG Goserelin
  • DRUG Imlunestrant
  • DRUG Tamoxifen 20 mg

Trial Details

FieldValue
Enrollment Target 600 participants
Start Date 2026-05-13
Est. Completion 2029-12
Phase Phase 2
Eli Lilly and Company

1,341 total trials

What NCT07287098 shows while recruiting

NCT07287098 is an interventional study that assigns participants to a tested intervention. The registered 600 participants enrollment target is mid-sized for trials with a published cap, above the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (351% higher).

The record links to 0 conditions, and to 3 interventions - of which Goserelin is the first listed.

NCT07287098 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT07287098 about?

NCT07287098 is a clinical study titled "A Study of Imlunestrant (LY3484356) in Premenopausal Women With Estrogen Receptor-Positive (ER+) Human Epidermal Growth Factor Receptor 2 Negative (HER2-) Early Breast Cancer". 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. S...

What is the current status of trial NCT07287098?

This trial is currently recruiting. It is a Phase 2 study. The enrollment target is 600 participants. The study started on 2026-05-13. Estimated completion is 2029-12.

What interventions are being tested in trial NCT07287098?

The interventions under investigation include: Goserelin (DRUG), Imlunestrant (DRUG), Tamoxifen 20 mg (DRUG).

Who is sponsoring clinical trial NCT07287098?

This trial is sponsored by Eli Lilly and Company, which has 1,341 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT07287098's enrollment target sits among peer trials

600 53rd of 2000 higher than 1,945 of 2,000 other Phase 2 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 2 trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

Nationwide trials with similar profiles

Cross-condition peers matched on enrollment target and registry start date, not the same-condition list above.

Similar enrollment target

  • NCT00004317 · 600 participants · Phase 4

    Pyrimethamine, Sulfadiazine, and Leucovorin in Treating Patients With Congenital Toxoplasmosis

  • NCT00209235 · 600 participants · NA

    Albright Hereditary Osteodystrophy: Natural History, Growth, and Cognitive/Behavioral Assessments

  • NCT01473784 · 600 participants · NA

    Transoral Robotic Surgery in Treating Patients With Benign or Malignant Tumors of the Head and Neck

  • NCT01866371 · 600 participants

    High Resolution Retinal Imaging

Similar registry start date

  • NCT05962346 · started 2026-12 · NA

    Fetal Endoscopic Tracheal Occlusion for Congenital Diaphragmatic Hernia

  • NCT07125183 · started 2026-12 · Phase 2

    Study on Efficacy and Tolerability of Weekly Doxorubicin in Elderly Patients With Advanced or Metastatic Leiomyosarcoma

  • NCT07292298 · started 2026-11 · Phase 2

    Phase 2 Single-Arm Rectal Cancer Brachytherapy for Patients With Low-Lying Residual Adenocarcinoma After Total Neoadjuvant Therapy to Improve Organ Preservation Rates

  • NCT04263285 · started 2026-10 · NA

    Treatment of Depression Post-SCI

Source: ClinicalTrials.gov NCT07287098, the US trial registry maintained by the National Library of Medicine. NCT07287098 (mid enrollment · none site footprint · recruiting) retrieved and formatted by PlainTrial, see methodology.