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NCT06907615
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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