Real-World study reveals gaps in lung cancer testing
NCT ID NCT05644808
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study follows over 1,000 people with newly diagnosed non-small cell lung cancer in community cancer clinics. Researchers want to see how many patients receive key biomarker test results before starting treatment, and what barriers (like tissue issues or insurance problems) cause delays. The goal is to understand real-world testing practices and improve access to personalized therapy.
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Study facts
What this study's own registry entry says, in plain language.
- Participants
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1,002 people
The number who actually took part.
- Started
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Dec 2020
- Expected to finish
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Dec 2027
An estimate. End dates often move.
- Lead sponsor
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A company
The lead sponsor is a pharmaceutical, biotech, or medical-device company.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
Who is studied
This pragmatic study looks to quantify the testing timeline, operational barriers, and outcomes of biomarker-guided therapy in a large, community-based, and largely unselected patient population with early stage and advanced stage, treatment naive non-small cell lung cancer.
- Ages
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18 years and older
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
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Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Adult subjects (18 years and older) with newly diagnosed early stage, locally advanced or metastatic non-small cell lung cancer * Eligible for systemic therapy based on the treating provider's assessment * Subjects who developed locally advanced or metastatic disease after receiving adjuvant or neoadjuvant therapy are eligible if the adjuvant/neoadjuvant therapy was completed at least 12 months prior to the development of locally advanced or metastatic disease * Subjects may be enrolled within 30 days of initiation of systemic therapy * Signed informed consent Exclusion Criteria: * Stage IA at the time of enrollment * Subjects with small cell lung cancer * Subjects with Unknown primary tumor origin
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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Illinois Cancer Specialists
Niles, Illinois, 60714, United States
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Maryland Oncology Hematology, P.A.
Silver Spring, Maryland, 20904, United States
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Minnesota Oncology Hematology, P.A.
Minneapolis, Minnesota, 55404, United States
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New York Oncology Hematology, P.C.
Albany, New York, 12208, United States
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Oncology Hematology Care Clinical Trials, LLC
Cincinnati, Ohio, 45242, United States
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Rocky Mountain Cancer Center
Denver, Colorado, 80218, United States
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Southern Cancer Center, PC
Daphne, Alabama, 36526, United States
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Texas Oncology - Fort Worth Cancer Center
Fort Worth, Texas, 76104, United States
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Texas Oncology - West Texas
Abilene, Texas, 79606, United States
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Texas Oncology- DFWW
Arlington, Texas, 76012, United States
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Texas Oncology- Northeast Texas
Tyler, Texas, 75702, United States
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Texas Oncology-Baylor Charles A. Sammons Cancer Center
Dallas, Texas, 75246, United States
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Texas Oncology-Dallas Presbyterian Hospital
Dallas, Texas, 75231, United States
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Texas Oncology-McAllen
McAllen, Texas, 78503, United States
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Virginia Cancer Specialists, PC
Fairfax, Virginia, 22031, United States
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Virginia Oncology Associates
Newport News, Virginia, 23606, United States
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Willamette Valley Cancer Institute and Research Center
Eugene, Oregon, 97401, United States
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Woodlands Medical Specialists, PA
Pensacola, Florida, 32503, United States
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