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Clinical Trial Summary

The purpose of this study is to evaluate the safety, tolerability and objective response rate of SKB264 as combination with therapy in subjects with advanced or metastatic non-small cell lung cancer.


Clinical Trial Description

This is a multicenter, open-label study of SKB264 as combination therapy in subjects with NSCLC. Approximately up to 296 subjects will be enrolled in this study including around 36 (may expand) subjects for safety run-in period and 200 subjects for expansion period. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05816252
Study type Interventional
Source Klus Pharma Inc.
Contact Xiaoping Jin, PhD
Phone 86-028-67255165
Email jinxp@kelun.com
Status Recruiting
Phase Phase 2
Start date April 19, 2023
Completion date August 31, 2026

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