drugset / Trial / NCT03644459
Safety and Efficacy of the Fully Humanized Anti - VEGF Monoclonal Antibody LYN00101
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
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | LYN00101 | Unknown | 8 mg/kg | Intravenous |
| Subject | LYN00101 | Unknown | 10 mg/kg | Intravenous |