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A Phase I Clinical Study to Evaluate the Safety, Tolerability, Pharmacokinetics, and Preliminary Pharmacodynamics of HLX22 Monoclonal Antibody Injection (HER2 Monoclonal Antibody) in Patients With Advanced Solid Tumours Overexpressing HER2

Trial Profile

A Phase I Clinical Study to Evaluate the Safety, Tolerability, Pharmacokinetics, and Preliminary Pharmacodynamics of HLX22 Monoclonal Antibody Injection (HER2 Monoclonal Antibody) in Patients With Advanced Solid Tumours Overexpressing HER2

Status: Completed
Phase of Trial: Phase I

Latest Information Update: 25 May 2023

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At a glance

  • Drugs HLX 22 (Primary)
  • Indications Solid tumours
  • Focus Adverse reactions; First in man
  • Sponsors Shanghai Henlius Biotech

Most Recent Events

  • 17 May 2023 Results presented in the Henlius Biopharmaceuticals Media Release.
  • 04 May 2023 Results (Between July 31, 2019, and December 27, 2021) assessing the safety, pharmacokinetics, pharmacodynamics, and preliminary efficacy of HLX22 in patients with advanced solid tumors who had failed or were intolerant to standard therapies, published in the Investigational New Drugs.
  • 29 Apr 2022 Status changed from active, no longer recruiting to completed.

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