RecruitingPhase 1NCT07140016

A Study of Gilteritinib in Adults With Advanced ALK-positive Non-small Cell Lung Cancer (NSCLC)

A Phase 1b Study of Gilteritinib in Participants With Locally Advanced or Metastatic NSCLC With ALK Rearrangement After Prior Treatment With an ALK Inhibitor


Sponsor

Astellas Pharma Global Development, Inc.

Enrollment

40 participants

Start Date

Sep 22, 2025

Study Type

INTERVENTIONAL

Conditions

Summary

Genes give your body instructions on how to make proteins. Proteins are needed to keep the body working properly. Many types of cancer are caused by changes in certain genes, making them faulty. Some people with non small cell lung cancer (NSCLC) have a faulty ALK gene. ALK stands for anaplastic lymphoma kinase. People with NSCLC who have the faulty ALK gene are called ALK-positive. ALK inhibitors are an approved treatment for people with ALK positive NSCLC. Some people stop responding to treatment with ALK inhibitors over time due to more changes happening in their faulty ALK gene, so there is an unmet medical need. Gilteritinib is an approved treatment for people with acute myeloid leukemia (AML) with the faulty FLT3 gene who haven't responded to previous treatment, or their cancer came back after previous treatment. Gilteritinib also blocks changes in the ALK gene which could help people with ALK-positive NSCLC. A study needs to be done with gilteritinib in people with ALK-positive NSCLC. The main aim of the study is to check the safety of gilteritinib in people with ALK-positive NSCLC and if they tolerate gilteritinib. People in this study will be adults with locally advanced or metastatic ALK-positive non-small cell lung cancer (NSCLC). Locally advanced means the cancer has spread to nearby tissue. Metastatic means the cancer has spread to other parts of the body. They have stopped responding to treatment with ALK inhibitors, including alectinib or lorlatinib, over time. The key reasons people cannot take part are if they have symptomatic cancers in the brain or nervous system, their cancer has spread to the thin tissue that covers the brain and spinal cord (leptomengingeal metastasis), have recently had or planning to have major surgery, have certain heart conditions, or have recently had an infection, a stroke or mini-stroke. People in the study will take tablets of gilteritinib once a day in a 28-day cycle. They may be given up to 2 different doses of gilteritinib. People in the study will start on the lower dose but can eventually switch to the higher dose if they tolerate the lower dose and meet the safety checks. Whilst taking gilteritinib, people will have regular scans of their tumors. People will continue taking gilteritinib until their cancer gets worse, they have medical problems from gilteritinib that they can't tolerate, they ask to stop taking gilteritinib, they start other cancer treatment or, sadly pass away. People will visit the clinic about 7 days and then 30 days after they stop taking gilteritinib. They will be asked about any medical problems and will have a safety check. After this, people who stopped taking gilteritinib, but their cancer hadn't become worse, will continue to have regular scans of their tumors. If their cancer does get worse, they will no longer have scans of their tumors. After finishing gilteritinib, people will be phoned every 12 weeks to check on their health. People will be in the study for up to 4 years, depending on how they respond to gilteritinib.


Eligibility

Min Age: 18 Years

Plain Language Summary

Simplified for easier understanding

This study is testing a drug called gilteritinib (already approved for leukemia) in people with advanced non-small cell lung cancer (NSCLC) that has a specific genetic change called an ALK rearrangement, and whose cancer has stopped responding to standard ALK inhibitor medications. **You may be eligible if...** - You have advanced or metastatic NSCLC confirmed by biopsy, with a documented ALK gene rearrangement - Your cancer is no longer responding to standard ALK inhibitor treatment - You have received at least one prior ALK inhibitor therapy - You are willing to provide a fresh tumor tissue sample before starting the study - Your general health and organ function meet the study criteria **You may NOT be eligible if...** - Your NSCLC does not have an ALK rearrangement - You have uncontrolled brain metastases - You have significant heart problems - You are pregnant or breastfeeding - You have had prior treatment with gilteritinib Talk to your doctor to see if this trial is right for you.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

DRUGgilteritinib

Oral


Locations(15)

University of California - Irvine

Orange, California, United States

Emory Winship Cancer Institute

Atlanta, Georgia, United States

OSF Health Care

Peoria, Illinois, United States

University of Michigan Health Systems

Ann Arbor, Michigan, United States

Washington University School of Medicine

St Louis, Missouri, United States

Hackensack University Medical Center

Hackensack, New Jersey, United States

UT Southwestern Medical Center at Dallas

Dallas, Texas, United States

Virginia Cancer Specialists PC

Fairfax, Virginia, United States

Site FR33008

Saint-Herblain, France

Site FR33005

Toulouse, France

Site FR33001

Villejuif, France

Site ES34017

Barcelona, Spain

Site ES34006

Madrid, Spain

Site ES34011

Madrid, Spain

Site ES34008

Málaga, Spain

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NCT07140016


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