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Brief Title: A Study to Investigate FP002 in Subjects With Advanced Malignancies
Official Title: A Phase 1 Study to Investigate the Safety, Efficacy, Pharmacokinetics, and Pharmacodynamics Activity of FP002 in Subjects With Advanced Malignancies
Study ID: NCT05982080
Brief Summary: The goal of this phase 1 study is to assess the safety, and tolerability of FP002 to determine the dose recommended for dose expansion in subjects with advanced solid tumor.
Detailed Description: This study is a phase 1 study of FP002 as monotherapy in patients with advanced solid tumor. The study will evaluate the safety, tolerability, pharmacokinetic, pharmacodynamic profile, immunogenicity, and preliminary anti-tumor activity of FP002 in patients with advanced solid tumors.
Minimum Age: 18 Years
Eligible Ages: ADULT, OLDER_ADULT
Sex: ALL
Healthy Volunteers: No
The First Affiliated Hospital of Xiamen University, Xiamen, Fujian, China
Shangdong Cancer Hospital & Institute, Jinan, Shangdong, China
Linyi Cancer Hospital, Linyi, Shangdong, China
Name: Yuping Sun, MD
Affiliation: Shangdong Cancer Hospital & Institute
Role: PRINCIPAL_INVESTIGATOR
Name: Linlin Wang, MD
Affiliation: Shangdong Cancer Hospital & Institute
Role: PRINCIPAL_INVESTIGATOR