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NCT06908928
A Dose Randomization Study of Bulumtatug Fuvedotin in TNBC Patients Previously Treated With ADCs
The goal of this clinical trial is to investigate if treatment with bulumtatug fuvedotin is effective in triple-negative breast cancer patients who have previously received treatment with an antibody-drug conjugates.
Trial Details
NCT ID NCT06908928
Phase PHASE1
Sponsor Mabwell (Shanghai) Bioscience Co., Ltd.
Status RECRUITING
Cancer Type Triple Negative (TNBC) Breast Cancer
Interventions
Locations (sample) Duarte, California, United States|34.13945,-117.97729 La Jolla, California, United States|32.84727,-117.2742 Aurora, Colorado, United States|39.72943,-104.83192 Chicago, Illinois, United States|41.85003,-87.65005 Boston, Massachusetts, United States|42.35843,-71.05977
Key Eligibility Criteria
Patient has measurable disease by RECIST v1.1 Recurrent or metastatic triple-negative breast cancer patients as per current ASCO/CAP guidelines Patient has received prior treatment with a taxane and an antibody-drug conjugate with a topoisomerase inhibitor payload. Patient has received no more than 3 prior lines of cytotoxic therapy in the locally advanced or metastatic setting.
For full eligibility, visit ClinicalTrials.gov .