Condition: Advanced Malignant Solid Tumors · Sponsor: Shanghai Junshi Bioscience Co., Ltd.
This is a multicenter, open-label Phase II clinical study. The primary objective is to evaluate the investigator-assessed objective response rate of JS212 and JS213 as monotherapy and in combination regimens in patients with advanced solid tumors. This study aims to explore the safety, tolerability, and preliminary efficacy of JS212, JS213, as well as JS212 in combination with JS213, toripalimab, and JS207.
This description comes directly from the study's public registry record.
Yuteng Shen, Project manager · 8618612107811 · yuteng_shen@junshipharma.com
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| Peking University Cancer Hospital | Beijing, Beijing Municipality, China | Recruiting |
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Source record: clinicaltrials.gov/study/NCT07480733