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OncoMatch/Clinical Trials/NCT06195709

ECLECTIC: EstroTEP and Circulating Biomarkers for ER-positive HER2-negative Metastatic Breast Cancer Patients

Is NCT06195709 recruiting? Yes, currently enrolling (May 2026). This Phase 3 trial studies multiple treatments including Endocrine therapy and Endocrine therapy combined with the local treatment of FES-negative lesions for breast carcinoma.

Phase 3RecruitingInstitut CurieNCT06195709Data as of May 2026

Treatment: Endocrine therapy · Endocrine therapy combined with the local treatment of FES-negative lesions · ChemotherapyEclectic is a strategy trial; once the class of treatment (endocrine therapy or chemotherapy) has been allocated according to 16α-18F-fluoro-17β-oestradiol (18F-FES) Positron Emission Tomography/Computed Tomography (PET/CT) results and circulating tumor biomarkers, clinicians will decide which treatment to use.

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Extracted eligibility criteria

Cancer type

Breast Carcinoma

Biomarker criteria

Required: ESR1 overexpression (ER-positive, ≥10%) (≥10%)

Estrogen Receptor (ER)-positive (≥10%)

Required: HER2 (ERBB2) negative

HER2-negative (ASCO/College of American Pathologists guidelines)

Disease stage

Metastatic disease required

Performance status

ECOG 0–2(Ambulatory, capable of self-care)

Prior therapy

Max 1 prior line
Min 1 prior line

Must have received: aromatase inhibitor — first line, metastatic

disease has progressed on first line endocrine therapy with aromatase inhibitor

Must have received: CDK4/6 inhibitor — first line, metastatic

disease has progressed on first line endocrine therapy with...CDK4/6 inhibitor

Cannot have received: chemotherapy

One or more prior line of chemotherapy in the metastatic setting [excluded]

Cannot have received: systemic treatment (other than first line aromatase inhibitor and CDK4/6 inhibitor)

Any other systemic treatment given at metastatic disease than the first line therapy with aromatase inhibitor and CDK4/6 inhibitor [excluded]

Cannot have received: estrogen receptor degrader (fulvestrant, oral SERDs, PROTAC)

Prior exposure to any authorized or experimental agent degrading the estrogen receptor (fulvestrant, oral SERDs, PROTAC, etc) [excluded]

Structured fields extracted by AI. May contain errors — verify against the official protocol.

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