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Clinical Trial Summary

The purpose of this study is to assess the safety and tolerability and preliminary antitumor activity of SKB264 with/without KL-A167 in patients with unresectable locally advanced, recurrent or metastatic TNBC and HR+/HER2- BC .The study is divided into three parts.Part 1(TNBC): exploratory phase of the efficacy and safety of the combination treatment. Part 2(TNBC): The subjects will be randomized to treatment group for SKB264 + KL-A167 or SKB264 . Part 3(HR+/HER2- BC): The subjects will be randomized to treatment group for SKB264 + KL-A167 or SKB264 .


Clinical Trial Description

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Study Design


Related Conditions & MeSH terms


NCT number NCT05445908
Study type Interventional
Source Sichuan Kelun Pharmaceutical Research Institute Co., Ltd.
Contact YiNa Diao
Phone 028-67252634
Email diaoyina@kelun.com
Status Recruiting
Phase Phase 2
Start date August 17, 2022
Completion date July 2025