48
Participants
Start Date
March 9, 2024
Primary Completion Date
December 31, 2029
Study Completion Date
December 31, 2030
IBD0333
This is a phase I/II, open, non-randomized, dose-escalation and expansion study designed to evaluate the safety, tolerability, pharmacokinetic (PK), immunogenicity, and preliminary efficacy of IBD0333 in patients with locally advanced/metastatic solid tumor or non-Hodgkin lymphoma in dose-escalation, dose-expansion, and clinical exploration phases.
RECRUITING
Affiliated Cancer Hospital of Shandong First Medical University, Jinan
SUNHO(China)BioPharmaceutical CO., Ltd.
INDUSTRY