Phase 1/2 Study to Evaluate EP0062 as Monotherapy and in Combination in Patients With Advanced or Metastatic AR+/HER-2-/ER+ Breast Cancer

The aim of this study is to identify the optimal dose for EP0062 as monotherapy and in combination with standard-of-care therapies to assess its Safety, Tolerability, Pharmacokinetics, and Efficacy in Patients with Relapsed Locally Advanced or Metastatic AR+/HER-2-/ER+ Breast Cancer

Trial Details

NCT ID
NCT05573126
Phase
PHASE1 / PHASE2
Sponsor
Ellipses Pharma
Status
RECRUITING
Cancer Type
HER2 Positive Breast Cancer
Interventions
  • EP0062
  • Elacestrant
  • Everolimus
  • Abemaciclib
  • Fulvestrant
  • Exemestane
Locations (sample)
  • New Haven, Connecticut, United States|41.30815,-72.92816
  • Tampa, Florida, United States|27.94752,-82.45843
  • Boston, Massachusetts, United States|42.35843,-71.05977
  • Detroit, Michigan, United States|42.33143,-83.04575
  • Nashville, Tennessee, United States|36.16589,-86.78444

Key Eligibility Criteria

  • Women 18 years or older at the time of informed consent
  • Histologically proven diagnosis of breast cancer with evidence of metastatic or locally advanced breast adenocarcinoma as defined by the American J…
  • Availability of archival tumour sample (formalin-fixed, paraffin-embedded block(s) or slides from a primary tumour or biopsy of a metastatic tumour…
  • Biopsy-proven AR+ and ER+ breast cancer

For full eligibility, visit ClinicalTrials.gov.

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