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Life sciences · Phase 1 Trial
ClinicalTrials.gov · October 23, 2026
No summary has been generated for this record yet. What follows is drawn from its source metadata only.
Phase 1 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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What is missing. This record has no bottom line, key findings, reported figures, evidence dimensions. That is a gap in the analysis, not a judgement about the study.
Registry record from ClinicalTrials.gov (NCT06908928). This is a study registration, not published results. Lead sponsor: Mabwell (Shanghai) Bioscience Co., Ltd.. Recruitment status: RECRUITING. Phase: PHASE1. Study type: INTERVENTIONAL. Enrollment: 52 participants (ESTIMATED). Conditions: Triple Negative Breast Cancer. Interventions: DRUG: bulumtatug fuvedotin; DRUG: bulumtatug fuvedotin. Primary outcome measures: Objective Response Rate , Up to approximately 2 years. Brief summary: 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.