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NCT06768931
Biolosion Combined Standard Neoadjuvant Therapy to Treat Triple-negative Breast Cancer
To evaluate the efficacy and safety of compound preparation Biolosion in combination with standard neoadjuvant therapy for locally advanced triple-negative breast cancer
Trial Details
NCT ID NCT06768931
Phase PHASE2
Sponsor Sun Yat-sen University
Status RECRUITING
Cancer Type Triple Negative (TNBC) Breast Cancer
Interventions Biolosion (oral probiotic compound preparation)
Locations (sample) Lanzhou, Gansu, China Dongguan, Guangdong, China Guangzhou, Guangdong, China Zhanjiang, Guangdong, China Zigong, Sichuan, China
Key Eligibility Criteria
Women aged 1.18 years and above, diagnosed with triple-negative breast cancer (ER≤10%, PR≤10%, HER-2 negative) by pathology; Patients must have tumor specimens (formalin-fixed, paraffin-embedded, or fresh pre-treated tumor tissue) available for PD-L1 expression testing; Researchers assess indications for neoadjuvant chemotherapy, with staging from IIA to IIIC, based on imaging or pathological evaluation of cT1c, N1… Patients must not have received chemotherapy or targeted therapy for advanced breast cancer;
For full eligibility, visit ClinicalTrials.gov .