Clinical Trials Directory

Trials / Completed

CompletedNCT05110118

Pharmacokinetic Characteristics, Safety, Tolerability and Immunogenicity of LY01008 and Avastin in Healthy Chinese Male Subjects

A Randomized, Double-blind, Single-dose, Parallel-group Study Comparing Pharmacokinetic Characteristics, Safety , Tolerability and Immunogenicity of LY01008 (Recombinant Humanized Anti-Human Vascular Endothelial Growth Factor Monoclonal Antibody Injection) and Avastin (Bevacizumab Injection) in Healthy Chinese Male Subjects

Status
Completed
Phase
Phase 1
Study type
Interventional
Enrollment
112 (actual)
Sponsor
Shandong Boan Biotechnology Co., Ltd · Industry
Sex
Male
Age
18 Years – 45 Years
Healthy volunteers
Accepted

Summary

This is a randomized, double-blind, single-dose, parallel-group study comparing pharmacokinetic characteristics, safety , tolerability and immunogenicity of LY01008 (Recombinant Humanized Anti-Human Vascular Endothelial Growth Factor Monoclonal Antibody Injection) and Avastin (Bevacizumab Injection) in healthy Chinese male subjects.

Conditions

Interventions

TypeNameDescription
DRUGLY01008Single intravenous injection
DRUGAvastinSingle intravenous injection

Timeline

Start date
2020-08-04
Primary completion
2021-01-13
Completion
2021-01-13
First posted
2021-11-05
Last updated
2021-11-05

Locations

1 site across 1 country: China

Source: ClinicalTrials.gov record NCT05110118. Inclusion in this directory is not an endorsement.