drugset / Trial / NCT06092086

Lorlatinib as the First-line Treatment in China Advanced ALK+ NSCLC

NCT06092086

Phase 2 Recruiting 126 enrolled Guangdong Association of Clinical Trials
NaSingle-groupOpen-labelTreatment

Summary

This phase II study is aim to investigate the efficacy, resistance mechanism, safety profile of first-line lorlatinib in China advanced ALK+ non-small cell lung cancer (NSCLC). Participants will receive continuous daily PO dosing of lorlatinib 100mg QD.

Timeline

Start
2023-08-18
Primary completion
2025-08-01
Completion
2030-08-01

Drugs

EvaluationDrugModalityDoseRoute
Subject Lorlatinib Small molecule 100 mg Oral