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Study identifier: NCT07739186 Synced from ClinicalTrials.gov · July 31, 2026
● Not Yet Recruiting

A Study Evaluating BL-B01D1 in Combination With a PD-1/VEGF Bispecific Antibody Versus Tislelizumab Plus Platinum-doublet Chemotherapy as First-line Treatment for Locally Advanced or Metastatic Non-squamous Non-small Cell Lung Cancer(PANKU-Lung06)

Condition: Non-squamous Non-small Cell Lung Cancer  ·  Sponsor: Sichuan Baili Pharmaceutical Co., Ltd.

PhasePhase 2/Phase 3
Planned participants120
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNo

About this study

This trial is a registrational randomized, open-label, multicenter Phase II/III study designed to evaluate the efficacy and safety of BL-B01D1 in combination with a PD-1/VEGF bispecific antibody in patients with locally advanced or metastatic non-squamous non-small cell lung cancer.

This description comes directly from the study's public registry record.

Talk to the study team

Sa Xiao, PHD  ·  15013238943  ·  xiaosa@baili-pharm.com

Always discuss trial participation with your own doctor first.

Locations (2)

Sun Yat-sen University Cancer CenterGuangzhou, Guangdong, China
The First Affiliated Hospital of Guangzhou Medical UniversityGuangzhou, Guangdong, China

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Source record: clinicaltrials.gov/study/NCT07739186