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Completed

NCT Number: NCT04411550

Compare Pharmacokinetics, Safety, and Immunogenicity of HLX11 vs. Perjeta in Healthy Chinese Male Subjects

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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Key information

Age range

18 year–45 year

Sex eligibility

Male

Study type

Interventional

Phase

Phase 1

Primary location

The Second Hospital of Anhui Medical University

Hefei, Anhui, China

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Healthy Chinese males
  • aged ≥ 18 and ≤ 45
  • body mass index (BMI) ≥ 19 and ≤ 26 kg/m2
  • LVEF≥ 55%

Exclusion criteria

  • A history of any serious clinical disease such as haematological, renal, endocrine, pulmonary, gastrointestinal, cardiovascular, hepatic, mental, neurological diseases, and tumour, or allergic diseases
  • Use of a monoclonal antibody or any biological product within 6 months before study drug administration
  • A history of allergic reactions or anaphylaxis, including such reactions to any drug or excipient in the clinical study
  • Use of prescription drugs, over-the-counter drugs (OTC), or traditional Chinese medicine (TCM) (excluding vitamins, mineral supplements, and dietary supplements) within 28 days before study drug administration
  • A history of blood donation within 3 months before study drug administration
  • Participation in other clinical study and use of the investigational product/comparator within 3 months before study drug administration
  • Positive for hepatitis B surface antigen (HbsAg), hepatitis C virus (HCV) antibody, human immunodeficiency virus (HIV) antibody, or treponema pallidum antibody
  • A history of drug abuse
  • Failure to comply with protocol requirements, instructions, and study limitations, such as uncooperative attitude, failure to return to the study site for follow-up visits, or failure to complete the entire clinical study, as judged by investigators

Treatment and study plan

HLX11

Drug

healthy volunteers receive HLX11 (420mg) once

CN-Perjeta(Pertuzumab)

Drug

healthy volunteers receive CN-Perjeta (420mg) once

EU-Perjeta(Pertuzumab)

Drug

healthy volunteers receive EU-Perjeta (420mg) once

US-Perjeta(Pertuzumab)

Drug

healthy volunteers receive US-Perjeta (420mg) once

Primary outcomes

  1. Cmax

    Time frame: from predose to 2352 hours (Day 99),13 timepoints

    Peak concentration

  2. AUC0~t

    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

  3. AUC0~inf

    Time frame: from predose to 2352 hours (Day 99),13 timepoints

    Area under the plasma concentration-time curve from time 0 to infinity

Secondary outcomes

  1. safety and tolerability of 4 groups

    Time frame: from day1 to day 99

    Number of participants with treatment-related adverse events as assessed by CTCAE v5.0

  2. safety and tolerability of 4 groups

    Time frame: from day1 to day 99

    Number of AE as assessed by CTCAE v5.0

  3. safety and tolerability of two groups

    Time frame: from day1 to day 99

    AE listing as assessed by CTCAE v5.0

Sponsors and collaborators

Lead sponsor

Shanghai Henlius Biotech

Industry

Registry information

Official study title

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

Important dates

Study start
2020
Primary completion
2021
Study completion
2021
First posted
Jun 2, 2020
Registry last updated
May 11, 2022

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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