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BREAST: ADJUVANT: ER+/HER2 neg: On Endocrine tx: EMBER-4

EMBER-4: A Randomized, Open-Label, Phase 3 Study of Adjuvant Imlunestrant vs Standard Adjuvant Endocrine Therapy in Patients Who Have Previously Received 2 to 5 Years of Adjuvant Endocrine Therapy for ER+, HER2- Early Breast Cancer With an Increased Risk of Recurrence

Title
Lilly J2J-MC-JZLH Adjuvant Breast EMBER-4
Study Title

EMBER-4: A Randomized, Open-Label, Phase 3 Study of Adjuvant Imlunestrant vs Standard Adjuvant Endocrine Therapy in Patients Who Have Previously Received 2 to 5 Years of Adjuvant Endocrine Therapy for ER+, HER2- Early Breast Cancer With an Increased Risk of Recurrence

Site Link
Malignancy
Breast cancer, IBC, ER+ breast cancer
Stage
Disease Setting
Adjuvant/Post-surgical
Line Of Therapy
Adjuvant
Investigational Agent
Imlunestrant
Drug Class
SERD
PI
Greg Vidal
Sponsor
Eli Lilly and Company
Phase
Status
Key Eligibility Criteria
Key Eligibility Criteria Details

Inclusion Criteria:

  • Have a diagnosis of ER+, HER2- early-stage, resected, invasive breast cancer without evidence of distant metastasis.
  • Participants must have received at least 24 months but not more than 60 months of any adjuvant ET, from time of adjuvant ET initiation.
  • Participants may have received (neo) adjuvant chemotherapy and/or targeted therapy with a CDK4/6- or PARP- inhibitor.
  • Must have an increased risk of disease recurrence based on clinical-pathological risk features.
  • Have a Performance Status of 0 or 1 on the Eastern Cooperative Oncology Group scale.
  • Have adequate organ function.

Exclusion Criteria:

  • Have any evidence of metastatic disease (including contralateral ALN) or inflammatory breast cancer at primary breast cancer diagnosis.
  • Participants with more than a 6-month consecutive gap in therapy during the course of prior adjuvant ET.
  • Participants who have completed or discontinued prior adjuvant ET >6 months prior to screening.
  • Participants with a history of previous breast cancer are excluded, with the exception of ipsilateral DCIS treated by locoregional therapy alone ≥5 years ago.
  • Pregnant, breastfeeding, or expecting to conceive or father children within the projected duration of the trial, starting with the screening visit through 180 days after the last dose of study intervention.
  • Participant has previously received ET of any duration for breast cancer prevention (tamoxifen or AIs) or raloxifene.
  • Participants with a history of any other cancer.
  • Have serious preexisting medical conditions that, in the judgment of the investigator, would preclude participation in this study.
Objective
  • Primary
    • Invasive Disease Free Survival
  • Secondary
    • Distant recurrence free survival
    • OS
    • PK
    • QOL
    • Safety
Assessment Frequency
_
Assessment Frequency 2
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Assessment Frequency Link
Path
invasive breast carcinoma, Estrogen receptor positive (ER+), HER2 negative
Dosing Frequency
Control Agents
Study Protocol
Randomized
Yes
X