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Study identifier: NCT05909332 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

Study of Antivascular Therapy Combined With Chemotherapy Versus Chemotherapy in Adjuvant Therapy of TNBC-BLIS Patients (BCTOP-T-A03)

Condition: Breast Cancer · Triple Negative Breast Cancer  ·  Sponsor: Fudan University

PhasePhase 3
Planned participants764
Who can joinFemale, 18 Years to 70 Years
Healthy volunteersNo

About this study

This is a randomized, open-label phase III clinical trial comparing antivascular therapy combined with standard chemotherapy and standard chemotherapy in adjuvant therapy for patients with triple-negative breast cancer, basal-like/Immune suppressed subtype.

This description comes directly from the study's public registry record.

Talk to the study team

Zhi-Ming Shao, MD, PhD  ·  +86-021-64175590  ·  zhimingshao@yahoo.com

Always discuss trial participation with your own doctor first.

Locations (15)

Beijing Cancer HospitalBeijing, Beijing Municipality, ChinaRecruiting
Chongqing Cancer HospitalChongqing, Chongqing Municipality, ChinaRecruiting
Fujian Medical University Union HospitalFuzhou, Fujian, ChinaRecruiting
Guangdong Academy of Medical Sciences Guangdong Provincial People's HospitalGuangzhou, Guangdong, ChinaRecruiting
Sun Yat-sen University Cancer CenterGuangdong, Guangzhou, ChinaRecruiting
Affiliated Hospital of Nantong UniversityNantong, Jiangsu, ChinaRecruiting
Northern Jiangsu People's HospitalYangzhou, Jiangsu, ChinaRecruiting
The First Hospital of China Medical UniversityShenyang, Liaoning, ChinaRecruiting
Liaoning Cancer Hospital & InstituteShenyang, Liaoning, ChinaRecruiting
Breast cancer institute of Fudan University Cancer HospitalShanghai, Shanghai Municipality, ChinaRecruiting
Shanghai Sixth People's Hospital Affiliated to Shanghai Jiaotong UniversityShanghai, Shanghai Municipality, ChinaRecruiting
Shanghai First Maternity and Infant HospitalShanghai, Shanghai Municipality, ChinaRecruiting

+ 3 more locations — full list on the registry record.

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Source record: clinicaltrials.gov/study/NCT05909332