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Brief Title: Clinical Study of PM1003 in Phase I/IIa Treatment of Advanced Malignant Solid Tumors
Official Title: Phase I Study to Evaluate the Tolerability, Safety, Pharmacokinetic and Primary Efficacy of PM1003 in Patients With Advanced Solid Tumors and Phase IIa Study to Evaluate the Primary Efficacy of PM1003 in Advanced Solid Tumors
Study ID: NCT05862831
Brief Summary: This is a single-arm, open-lable, multicenter phase I/IIa clinical trial evaluating the safety, tolerability, pharmacokinetics, and preliminary efficacy of PM1003 in the treatment of advanced solid tumors.
Detailed Description: PM1003 is a Bispecific Antibody Targeting PD-L1 and 4-1BB.
Minimum Age: 18 Years
Eligible Ages: ADULT, OLDER_ADULT
Sex: ALL
Healthy Volunteers: No
Cancer Hospital Affiliated to Shandong First Medical University, Jinan, Shandong, China
Shanghai Orient Hospital, Shanghai, , China
Name: Ye Guo
Affiliation: Shanghai Orient Hospital
Role: PRINCIPAL_INVESTIGATOR