Lorlatinib for ALK-Positive Advanced Non-Small Cell Lung Cancer

This study is looking at a drug called lorlatinib for people with advanced non-small cell lung cancer (NSCLC) that has a specific change in the ALK gene. Lorlatinib is a type of medicine called a kinase inhibitor, which targets certain proteins in cancer cells. You might be able to join if you have stage IV or recurrent NSCLC and your cancer has the ALK gene change, confirmed by specific tests. The study will first treat participants with lorlatinib for 12 weeks. Researchers want to see if adding local consolidation therapy (LCT) to lorlatinib helps people live longer without their cancer getting worse, and they will also look at the safety of these treatments. The study aims to enroll 30 participants, but its current status is unclear.

Study design
This is an open-label, multicenter, randomized phase 2 trial. It plans to enroll 30 participants.
What's involved
Not specified in the trial record.
Compensation
Not stated in the trial record.
Follow-up
Safety and adverse events will be measured through study completion, which is an average of 1 year.

AI-generated from the public study record. Only the study team can confirm whether you're eligible — confirm details with them before making decisions.

NCT07415005

Lorlatinib Plus Local Consolidation Therapy In ALK Positive Advanced Non-Small Cell Lung Cancer

Recruiting
PHASE2Ages 18+InterventionalTreatment
M.D. Anderson Cancer Center
~30 participants
Updated 2026-05-05 on ClinicalTrials.gov
What's tested:Lorlatinib

At a glance

Recruiting sites
1 of 1 listed site is recruiting right now
RecruitingSuspended, closed, or not yet open
What they're measuring
Safety and Adverse Events (AEs)
Measured over Through study completion; an average of 1 year
Advanced Non-Small Cell Lung Cancer
1 sites across 1 states
Texas1
  • Yasir Y Elamin, MD · PRINCIPAL_INVESTIGATOR · M.D. Anderson Cancer Center

Opens a ready-to-send draft in your own email app — review before sending.

  • Safety and Adverse Events (AEs)Through study completion; an average of 1 year

    Incidence of Adverse Events, Graded According to National Cancer Institute Common Terminology Criteria for Adverse Events (NCI CTCAE) Version (v) 6.0