drugset / Trial / NCT06092086
Lorlatinib as the First-line Treatment in China Advanced ALK+ NSCLC
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
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | Lorlatinib | Small molecule | 100 mg | Oral |