Overview

Safety and Pharmacokinetics Study of YYB101 in Advanced Solid Tumors Patients Who Are Refractory to Standard Therapy

Status:
Completed
Trial end date:
2018-07-04
Target enrollment:
Participant gender:
Summary
The purpose of this study is to evaluate the safety, tolerability, pharmacokinetics, and maximum tolerated dose (MTD) of YYB101, HGF-neutralizing humanized Mab, in advanced solid tumors patients who are refractory to standard therapy.
Phase:
Phase 1
Details
Lead Sponsor:
CellabMED
National OncoVenture
Collaborator:
Yooyoung Pharmaceutical Co.,Ltd.