drugset / Trial / NCT05577702

Efficacy, Safety, and Pharmacodynamics of Tislelizumab Monotherapy and Multiple Tislelizumab-based Immunotherapy Combinations in Participants With Resectable Non-Small Cell Lung Cancer

NCT05577702

Phase 2 Completed 121 enrolled BeiGene
RandomizedParallel-groupOpen-labelTreatment

Summary

This study was conducted to evaluate the preliminary effectiveness and safety of treatment with tislelizumab alone and in combination with other investigational agents prior to surgery (neoadjuvant treatment) in adults with non-small cell lung cancer (NSCLC) that is able to be removed by surgery.

Timeline

Start
2023-03-08
Primary completion
2024-12-13
Completion
2025-01-23

Drugs

EvaluationDrugModalityDoseRoute
Subject Alcestobart Monoclonal antibody 600 mg Intravenous
Subject Carboplatin Small molecule Intravenous
Subject Cisplatin Other / unclassified 75 mg/m2 Intravenous
Subject Ociperlimab Monoclonal antibody 900 mg Intravenous
Subject Paclitaxel Small molecule 175 mg/m2 Intravenous
Subject Pemetrexed Small molecule 500 mg/m2 Intravenous
Subject Tislelizumab Monoclonal antibody 200 mg Intravenous