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Clinical Trial Summary

This is a Phase I open-label, multicenter study to evaluate the safety, tolerability, pharmacokinetics (PK),Pharmacodynamic characteristics, immunogenicity and antitumor activity of JS207 in patients with advanced malignant tumor. The Recommended dose for phase II trial (RP2D) will be determined based on the safety, tolerability, pharmacokinetics.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT06022250
Study type Interventional
Source Shanghai Junshi Bioscience Co., Ltd.
Contact Kai Xu
Phone 86 13761020175
Email kai_xu@junshipharma.com
Status Not yet recruiting
Phase Phase 1
Start date September 15, 2023
Completion date March 15, 2026

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