A Phase II Clinical Study to Evaluate HLX43 in Subjects With Advanced Non-small Cell Lung Cancer (NSCLC)

The study is being conducted to to explore the reasonable dosage and evaluate the efficacy, safety and tolerability of HLX43 (Anti-PD-L1 ADC) in Patients with Advanced Non-small Cell Lung Cancer (NSCLC)

Trial Details

NCT ID
NCT06907615
Phase
PHASE2
Sponsor
Shanghai Henlius Biotech
Status
RECRUITING
Cancer Type
Lung Cancer
Interventions
  • HLX43 DOSE 1 (2.0 mg/kg)
  • HLX43 DOSE 2 (2.5 mg/kg)
Locations (sample)
  • Houston, Texas, United States|29.76328,-95.36327
  • Beijing, Beijing Municipality, China|39.9075,116.39723

Key Eligibility Criteria

  • Have a full understanding of the study content, process, and possible adverse reactions before the study, and sign the informed consent form (ICF);…
  • Aged ≥ 18 years at the time of signing the ICF, male or female;
  • Histologically or cytologically confirmed, locally advanced (stage IIIB/IIIC) or metastatic (stage IV) NSCLC not suitable for radical treatment (co…
  • Subjects without actionable genomic alterations (AGAs):

For full eligibility, visit ClinicalTrials.gov.

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