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Clinical Trial Summary

The study is being conducted to evaluate safety, tolerability, pharmacokinetics and preliminary efficacy of PM1032 for patients with advanced tumors, also to explore the recommended Phase Ⅱ Dose(RP2D) of PM1032.


Clinical Trial Description

PM1032 is a Bispecific Antibody Targeting CLDN18.2 and 4-1BB. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05839106
Study type Interventional
Source Biotheus Inc.
Contact Xiying Dong
Phone +86 13867126972
Email dong.xy@biotheus.com
Status Recruiting
Phase Phase 1/Phase 2
Start date July 8, 2022
Completion date December 31, 2025

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