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Clinical Trial Summary

This is a Phase I open-label, multicenter study to evaluate the safety, tolerability, pharmacokinetics (PK), immunogenicity and antitumor activity of JS015 in patients with advanced solid tumors. The Recommended dose for phase II trial (RP2D) was determined based on the safety, pharmacokinetics, and initial efficacy data of the dose escalation and extension.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT05770310
Study type Interventional
Source Shanghai Junshi Bioscience Co., Ltd.
Contact Kai Xu, Project manager
Phone +86 13761020175
Email kai_xu@junshipharma.com
Status Recruiting
Phase Phase 1
Start date February 1, 2023
Completion date July 1, 2025

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