Cemiplimab in High-risk or Locally Advanced Luminal and Triple Negative Breast Cancer

Фаза 2 Идёт, набор закрыт NCT04243616

Кратко

This is a single-arm, open-label, phase 2 study that will enroll 36 subjects, who have pathologically proven diagnosis of invasive breast cancer, clinical stage tumor 1-3 (cT1-T3), node 0-3 (cN0-N3), metastasis 0 (cM0), hormone receptor positive (HR+) (estrogen-receptor-positive (ER+) and/or progesterone-receptor-positive (PR+) human epidermal growth factor receptor 2 (HER2) negative or hormone receptor-negative (HR-) (estrogen-receptor-negative (ER-) and progesterone-receptor-negative (PR-) human epidermal growth factor receptor 2 (HER2) negative/triple-negative breast cancer.

The Proportion of Breast Cancer Patients With Pathological Complete Response (pCR).

27 weeks from start of treatment · percentage of subjects

Открыть в BENITIONS Открыть на ClinicalTrials.gov

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