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Life sciences · Phase 2 Trial
ClinicalTrials.gov · October 20, 2026
No summary has been generated for this record yet. What follows is drawn from its source metadata only.
Phase 2 Trial.
No findings were extractable from the material analysed.
Safety was not reported in the material analysed. Check the source before drawing any conclusion about harm.
The source did not state who this applies to in practice.
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Registry record from ClinicalTrials.gov (NCT04243616). This is a study registration, not published results. Lead sponsor: Medical College of Wisconsin. Recruitment status: ACTIVE_NOT_RECRUITING. Phase: PHASE2. Study type: INTERVENTIONAL. Enrollment: 36 participants (ACTUAL). Conditions: Invasive Breast Cancer. Interventions: DRUG: Cemiplimab; DRUG: Paclitaxel; DRUG: Carboplatin (not mandatory); DRUG: Doxorubicin; DRUG: Cyclophosphamide. Primary outcome measures: The Proportion of Breast Cancer Patients With Pathological Complete Response (pCR). , 27 weeks from start of treatment. Brief summary: 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.