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Clinical Trial Summary

This study will look at the efficacy and safety of QL1706 plus albumin-bound paclitaxel and carboplatin in a neoadjuvant setting, in high-risk, TNBC early breast cancer.


Clinical Trial Description

This study is a single-arm, single-center, phase II clinical study designed to observe and evaluate the efficacy and safety of QL1706 combined with Pcb regimen in the neoadjuvant treatment of early-stage high-risk TNBC breast cancer. It is planned to enroll 73 subjects. After the subjects are enrolled in the study, they will receive 6 cycles of QL1706 combined with PCb regimen. A 3-week treatment cycle is used until the treatment termination event specified in the protocol occurs. The subjects will continue to undergo postoperative efficacy and safety visits after ending of the treatment. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT06404736
Study type Interventional
Source Fudan University
Contact Zhi-Ming Shao, MD, PhD
Phone +86-021-64175590
Email zhi_ming_shao@163.com
Status Not yet recruiting
Phase Phase 2
Start date May 7, 2024
Completion date November 7, 2030

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