drugset / Trial / NCT07134413

QL1706/Bevacizumab ± Chemotherapy in Post-ICI Non-Squamous NSCLC

NCT07134413

Phase 2 Not yet recruiting 77 enrolled Guangdong Association of Clinical Trials
Non-randomizedSingle-groupOpen-labelTreatment

Summary

The goal of this clinical trial is to evaluate QL1706 plus bevacizumab with or without chemotherapy in patients with PD-L1-negative, locally advanced or metastatic non-squamous non-small cell lung cancer (NSCLC) previously treated with immune checkpoint inhibitors (ICIs). The primary objectives are: To assess the efficacy and safety of QL1706 combined with bevacizumab (± chemotherapy) in this population. Eligible patients with PD-L1-negative, locally advanced or metastatic non-squamous NSCLC who progressed after prior PD-1/PD-L1 inhibitor therapy will be assigned to one of two treatment arms at the investigator's discretion: Arm 1: QL1706 + bevacizumab + chemotherapy (target enrollment: 67 subjects). Single-agent chemotherapy (selected from regimens not previously received) will be administered, with options including nab-paclitaxel, pemetrexed, or docetaxel. Arm 2: QL1706 + bevacizumab (target enrollment: 10 subjects).

Timeline

Start
2025-08
Primary completion
2027-10
Completion
2029-07

Drugs

EvaluationDrugModalityDoseRoute
Subject Bevacizumab Monoclonal antibody 15 mg/kg
Subject Docetaxel Small molecule
Subject Paclitaxel Small molecule
Subject Pemetrexed Small molecule
Subject QL1706 Monoclonal antibody 5 mg/kg