A Phase I Clinical Study Evaluating the Safety, Tolerability, Pharmacokinetic Characteristics and Initial Efficacy of HLX35 (Recombinant Human Anti-EGFR and Anti-4-1BB Bispecific Antibody) in Patients With Advanced or Metastatic Solid Tumors

Status: Active, no longer recruiting

Phase of Trial: Phase I

Latest Information Update: 10 Aug 2023

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At a glance

Drugs HLX 35 (Primary)
Indications Non-small cell lung cancer; Solid tumours; Squamous cell cancer
Focus Adverse reactions; First in man
Sponsors Shanghai Henlius Biotech

Most Recent Events

07 Aug 2023 Status changed from recruiting to active, no longer recruiting.
07 Jun 2022 According to a Shanghai Henlius Biotech media release, Status changed from not yet recruiting to recruiting.
07 Jun 2022 According to a Shanghai Henlius Biotech media release, the first subject was dosed

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