Fluorine-18-AlphaVBeta6-Binding Peptide Positron Emission Tomography in Metastatic Non-Small Cell Lung Cancer
Launched by UNIVERSITY OF CALIFORNIA, DAVIS · Jul 6, 2022
Trial Information
Current as of June 26, 2025
Recruiting
Keywords
ClinConnect Summary
This clinical trial is exploring a new imaging tool called fluorine-18-AlphaVBeta6-BP ([18F]-αvβ6-BP) to help doctors see and assess the extent of Non-Small Cell Lung Cancer (NSCLC) in patients, particularly those with brain metastases (cancer that has spread to the brain). The researchers believe that this imaging method, combined with a standard scan called Positron Emission Tomography (PET) and Computed Tomography (CT), can provide clearer information about the disease, which may help in planning further treatment.
To participate in this trial, individuals must be over 18 years old and have a confirmed diagnosis of NSCLC that has spread to the brain, whether or not it has already been treated. Participants should be able to undergo the required imaging procedures, which may last between 30 to 60 minutes. They will also need to have certain health checks done within a few weeks before joining the study. It’s important to note that pregnant women, prisoners, and those with specific other health conditions are not eligible for this trial. If you or a loved one is interested, the study is currently recruiting participants and aims to provide valuable insights into more effective cancer imaging.
Gender
ALL
Eligibility criteria
- Inclusion Criteria:
- • 1. Men and women age \>18 yrs
- • 2. Biopsy proven NSCLC with brain metastases (treated or untreated)
- • 3. Life-expectancy of ≥3 months in the opinion of the treating physician
- • 4. Available archival tumor tissue (excisional, core, or fine needle aspiration (FNA) is acceptable). Tissue from a metastatic site is preferred when available.
- • 5. Able to tolerate all study procedures, including remain motionless for up to 30-60 minutes per scan
- • 6. Ability to understand and willingness to sign a written informed consent document.
- • 7. Planned to undergo additional cancer-directed therapy followed by standard-of-care re-staging imaging
- • 8. \[18F\]-FDG PET/CT within 21 days of enrollment
- • 9. MRI brain within 21 days of enrollment
- • 10. Eastern Cooperative Oncology Group Performance Status ≤ 2
- • 11. Glomerular filtration rate (GFR) ≥ 60
- Exclusion Criteria:
- • 1. Pregnant or lactating women
- • 2. Prisoners
- • 3. Concurrent malignancy of a different histology that could confound imaging interpretation
- • 4. Patients who cannot undergo PET/CT scanning because of weight limits(\>350lbs)
About University Of California, Davis
The University of California, Davis (UC Davis) is a leading research institution renowned for its commitment to advancing healthcare through innovative clinical trials and studies. With a strong focus on interdisciplinary collaboration, UC Davis leverages its extensive expertise in medical research, education, and patient care to drive breakthroughs in various fields, including medicine, public health, and agriculture. The university's clinical trial programs emphasize rigorous scientific methodology and ethical standards, aiming to translate research findings into impactful treatments and improved patient outcomes. Through its state-of-the-art facilities and a dedicated team of researchers and healthcare professionals, UC Davis is at the forefront of transforming healthcare practices and addressing critical health challenges.
Contacts
Jennifer Cobb
Immunology at National Institute of Allergy and Infectious Diseases (NIAID)
Locations
Sacramento, California, United States
Patients applied
Trial Officials
Julie L. Sutcliffe, PhD
Principal Investigator
The Regents of the University of California (Davis)
Timeline
First submit
Trial launched
Trial updated
Estimated completion
Not reported
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