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Life sciences · Phase 2 Trial
ClinicalTrials.gov · September 21, 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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This record has not been graded across any dimension yet. Treat the label above as provisional and read the source.
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 (NCT04734262). This is a study registration, not published results. Lead sponsor: Fudan University. Recruitment status: ACTIVE_NOT_RECRUITING. Phase: PHASE2. Study type: INTERVENTIONAL. Enrollment: 98 participants (ACTUAL). Conditions: Metastatic Breast Cancer. Interventions: DRUG: Sitravatinib; DRUG: Tislelizumab; DRUG: Nab-paclitaxel. Primary outcome measures: Overall Response Rate (ORR) by Investigator in Cohort A, Cohort B and Cohort C , Up to 12 months; Number of participants experiencing ≥ Grade 3 TRAEs in Cohort B , Up to 12 months. Brief summary: The purpose of this study is to assess the efficacy and safety of sitravatinib plus tislelizumab or combination with nab-paclitaxel in locally recurrent or metastatic triple-negative breast cancer (TNBC) patients.