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Clinical Trial Summary

This is a Phase 1/2, open-label, multicenter study designed to evaluate the safety, tolerability, and DLTs to establish the maximum tolerated dose (MTD) or maximum administered dose (MAD), and the RP2D of sequential doses of IBI354 (study drug), and to explore and confirm the efficacy, safety and tolerability of IBI354 in subjects with locally advanced unresectable or metastatic solid tumors.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT05636215
Study type Interventional
Source Innovent Biologics (Suzhou) Co. Ltd.
Contact Peng An
Phone +86 18310080353
Email alisa.an@innoventbio.com
Status Not yet recruiting
Phase Phase 1/Phase 2
Start date January 1, 2023
Completion date July 15, 2025