drugset / Trial / NCT03644459

Safety and Efficacy of the Fully Humanized Anti - VEGF Monoclonal Antibody LYN00101

NCT03644459 ↗

Phase 1 Withdrawn Lynkcell Inc.
NaSingle-groupOpen-labelTreatment

Summary

The purpose of this study is evaluate the pharmacokinetics, pharmacodynamics, immunogenicity and anti-tumor effect of of fully human anti - VEGF monoclonal antibody LY00101 and explore the potential prognostic and predictive biomarkers. This study will not take into account the results of molecular-genetic tests of patients enrolled in the study

Timeline

Start
2019-04-03
Primary completion
2020-06
Completion
2020-08

Outcome

Outcome not reported

Stopped (Enrollment): “Unable to recruit individuals for the study”

Drugs

EvaluationDrugModalityDoseRoute
Subject LYN00101 Unknown 8 mg/kg Intravenous
Subject LYN00101 Unknown 10 mg/kg Intravenous