RecruitingPhase IEN originalLung cancerMetastatic / advanced

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

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This is not medical advice. AI-assisted translation — inaccuracies may occur. Always verify the original and consult your oncologist before taking any steps.

About the trial

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.

Original English text from ClinicalTrials.gov

Who can (and can't) join

✓ Qualifies

  • Potwierdzony histologicznie lub cytologicznie zaawansowany rak płuca (NSCLC) z mutacją genu ALK
  • Wcześniejsze leczenie co najmniej jednym inhibitorem ALK (np. alectinib lub lorlatinib)
  • Choroba rozwinęła się lub wznowiła się podczas ostatniego leczenia lub po jego zakończeniu
  • Mierzalne zmiany nowotworu widoczne w badaniach obrazowych
  • Ogólny stan zdrowia pozwalający na uczestnictwo w badaniu (ECOG ≤ 2)
  • Kobieta nie może być w ciąży i musi mieć negatywny test ciążowy

✗ Disqualifies

  • Nowotwór rozprzestrzeniony na mózg lub oponę mózgową powodujący objawy
  • Planowana lub niedawno przeprowadzona poważna operacja
  • Zaburzenia serca uniemożliwiające uczestnictwo
  • Niedawny udar mózgu lub zawał
  • Świeża poważna infekcja

Simplified criteria — AI translation

Trial details

Minimum age
18 Years
Last updated (source)
August 17, 2026
Sex
No restrictions

Therapies / drugs in trial

Locations (17)

Providence Medical Foundation - Fullerton - Virginia K. Crosson Cancer Center

Fullerton, United States

University of California - Irvine

Orange, United States

Vail Health Hospital - Shaw Cancer Center

Edwards, United States

Emory Winship Cancer Institute

Atlanta, United States

OSF Health Care

Peoria, United States

University of Michigan Health Systems

Ann Arbor, United States

Washington University School of Medicine

St Louis, United States

Hackensack University Medical Center

Hackensack, United States

UT Southwestern Medical Center at Dallas

Dallas, United States

Virginia Cancer Specialists PC

Fairfax, 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

Trial contact

Astellas Pharma Global Development, Inc.

Contact information from ClinicalTrials.gov. Contact in English.

Share this trial

Data from ClinicalTrials.gov. AI-assisted translation, last sync: 8/18/2026.

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