The Second Hospital of Anhui Medical University
Hefei, Anhui, China
NCT Number: NCT04411550
This is a randomised, double-blind, intravenous single-dose, four-arm parallel study designed to compare the PK of HLX11 and US, EU, and CN-sourced Perjeta® in healthy Chinese adult male subjects, and to assess the safety, tolerability, and immunogenicity of these 4 drugs.
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Notify Me18 year–45 year
Male
Interventional
Phase 1
Hefei, Anhui, China
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
healthy volunteers receive HLX11 (420mg) once
healthy volunteers receive CN-Perjeta (420mg) once
healthy volunteers receive EU-Perjeta (420mg) once
healthy volunteers receive US-Perjeta (420mg) once
Time frame: from predose to 2352 hours (Day 99),13 timepoints
Peak concentration
Time frame: from predose to 2352 hours (Day 99),13 timepoints
Area under the plasma concentration-time curve from time 0 to the last concentration-measurable time point
Time frame: from predose to 2352 hours (Day 99),13 timepoints
Area under the plasma concentration-time curve from time 0 to infinity
Time frame: from day1 to day 99
Number of participants with treatment-related adverse events as assessed by CTCAE v5.0
Time frame: from day1 to day 99
Number of AE as assessed by CTCAE v5.0
Time frame: from day1 to day 99
AE listing as assessed by CTCAE v5.0
Shanghai Henlius Biotech
Industry
A (Randomised, Double-Blind, Intravenous Single-Dose, Parallel, Four-Arm) Phase I Clinical Study to Compare Pharmacokinetics, Safety, and Immunogenicity of HLX11 vs. Perjeta® (US, EU, and CN-Sourced) in Healthy Chinese Male Subjects
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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