Overview

A Study to Compare SB17 (Proposed Ustekinumab Biosimilar) to European Union (EU) Sourced Stelara and United States of America (US) Sourced Stelara in Healthy Subjects

Status:
Recruiting
Trial end date:
2021-09-07
Target enrollment:
Participant gender:
Summary
This is a randomised, double-blind, three-arm, parallel group, single-dose study to evaluate the pharmacokinetics, safety, tolerability, and immunogenicity of SB17 compared to EU sourced Stelara® and US sourced Stelara® in healthy subjects
Phase:
Phase 1
Details
Lead Sponsor:
Samsung Bioepis Co., Ltd.
Treatments:
Ustekinumab