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MYLUNG Consortium Study Protocol 2
NCT05644808 · View on ClinicalTrials.gov ↗
Study Summary
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, whether squamous or non-squamous.
Conditions Studied
Study Locations (18)
Texas
- Texas Oncology - West Texas — Abilene
- Texas Oncology- DFWW — Arlington
- Texas Oncology-Dallas Presbyterian Hospital — Dallas
- Texas Oncology-Baylor Charles A. Sammons Cancer Center — Dallas
- Texas Oncology - Fort Worth Cancer Center — Fort Worth
- Texas Oncology-McAllen — McAllen
- Texas Oncology- Northeast Texas — Tyler
Virginia
- Virginia Cancer Specialists, PC — Fairfax
- Virginia Oncology Associates — Newport News
Alabama
- Southern Cancer Center, PC — Daphne
Colorado
- Rocky Mountain Cancer Center — Denver
Florida
- Woodlands Medical Specialists, PA — Pensacola
Illinois
- Illinois Cancer Specialists — Niles
Maryland
- Maryland Oncology Hematology, P.A. — Silver Spring
Minnesota
- Minnesota Oncology Hematology, P.A. — Minneapolis
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 1,002 participants |
| Start Date | 2020-12-29 |
| Est. Completion | 2027-12 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT05644808
The ClinicalTrials.gov registry entry for NCT05644808 describes a study currently listed as active not recruiting. It is categorized as an unspecified phase, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 1,002 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is US Oncology Research, which has 9 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.
The record links to 1 condition, with Carcinoma, Non-Small-Cell Lung appearing as the primary indexed condition, and to 0 interventions. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.
Geographic footprint matters for practical reasons: NCT05644808 reports 18 study locations spanning 11 distinct geographic areas — top geographies include Texas, Virginia, Alabama. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.
Frequently Asked Questions
What is clinical trial NCT05644808 about?
NCT05644808 is a clinical study titled "MYLUNG Consortium Study Protocol 2". 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, whether squamous or non-...
What is the current status of trial NCT05644808?
This trial is currently active not recruiting. The enrollment target is 1,002 participants. The study started on 2020-12-29. Estimated completion is 2027-12.
What conditions does trial NCT05644808 study?
This clinical trial studies the following conditions: Carcinoma, Non-Small-Cell Lung. These conditions were identified from the trial registry and reflect the primary focus areas of the research.
Who is sponsoring clinical trial NCT05644808?
This trial is sponsored by US Oncology Research, which has 9 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.
Where is trial NCT05644808 being conducted?
This trial has 18 study locations across Alabama, Colorado, Florida, Illinois, Maryland. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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