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UnknownNCT03115762

Pharmacokinetics and Safety Study of ASKB1202 in Chinese Healthy Subjects

Pharmacokinetics,Safety and Immunogenicity of ASKB1202 in Chinese Healthy Subjects: a Randomized, Double-blinded, Single-dose, Parallel-arm, Active-comparator Clinical Phase I Study

Status
Unknown
Phase
Phase 1
Study type
Interventional
Enrollment
126 (estimated)
Sponsor
Jiangsu Aosaikang Pharmaceutical Co., Ltd. · Industry
Sex
Male
Age
18 Years – 50 Years
Healthy volunteers
Accepted

Summary

This trial will investigate the pharmacokinetic,immunogenicity and safety biosimilarity of ASKB1202 compared to bevacizumab sold in China and Europe.

Conditions

Interventions

TypeNameDescription
BIOLOGICALbevacizumabrecombinant humanized monoclonal antibody produced by DNA technology in Chinese Hamster Ovary cells
BIOLOGICALASKB1202

Timeline

Start date
2017-06-01
Primary completion
2017-07-01
Completion
2017-07-01
First posted
2017-04-14
Last updated
2017-04-14

Source: ClinicalTrials.gov record NCT03115762. Inclusion in this directory is not an endorsement.