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18F-αvβ6-BP for Cancer

Phase < 1
Waitlist Available
Led By Julie Sutcliffe
Research Sponsored by Julie L. Sutcliffe, Ph.D
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
Diagnosed with primary or metastatic cancer in one or more of the following locations: breast, colorectal, lung, pancreas
Eastern Cooperative Oncology Group (ECOG) performance score of 0-1
Must not have
Women who are pregnant or breast-feeding
Timeline
Screening 3 weeks
Treatment Varies
Follow Up up to 6 months
Awards & highlights
No Placebo-Only Group

Summary

This trial studies the side effects of a radiotracer called 18F-alphavbeta6-binding-peptide and how well it works in imaging patients with primary or cancer that has spread to the breast, colorectal, lung, or pancreatic.

Who is the study for?
This trial is for people with primary or metastatic breast, colorectal, lung, or pancreatic cancer who can stay still for PET scans and have a good performance status. It's not for those with severe kidney/liver issues, very short life expectancy, pregnant/breastfeeding women, recent investigational drug use, or inability to undergo PET/CT scans.
What is being tested?
The study tests the safety and imaging effectiveness of a radiotracer called 18F-αvβ6-binding-peptide in detecting cancers such as breast, colorectal, lung and pancreatic when used during PET scans.
What are the potential side effects?
Specific side effects are not listed but generally include potential reactions to the radiotracer like rash or discomfort at injection site. The scan procedure may cause discomfort from staying still.

Eligibility Criteria

Inclusion Criteria

You may be eligible if you check “Yes” for the criteria below
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My cancer is in the breast, colorectal, lung, or pancreas.
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I am fully active or have some restrictions but can still care for myself.
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I can stay still for up to an hour.

Exclusion Criteria

You may be eligible for the trial if you check “No” for criteria below:
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I am currently pregnant or breastfeeding.

Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~up to 6 months
This trial's timeline: 3 weeks for screening, Varies for treatment, and up to 6 months for reporting.

Treatment Details

Study Objectives

Study objectives can provide a clearer picture of what you can expect from a treatment.
Primary study objectives
Assessment of safe administration of 18F-αvβ6-BP
Secondary study objectives
Level of αvβ6-BP expression in tumors
Measurement of 18F-αvβ6-BP accumulation in tumors

Awards & Highlights

No Placebo-Only Group
All patients enrolled in this study will receive some form of active treatment.

Trial Design

1Treatment groups
Experimental Treatment
Group I: 18F-αvβ6-BPExperimental Treatment1 Intervention
Patients receive 18F-alphavbeta6-BP IV and then undergo 4 PET scans over 30 minutes each at 30, 60, 120, and 180 minutes post-injection.

Find a Location

Who is running the clinical trial?

Julie L. Sutcliffe, Ph.DLead Sponsor
National Cancer Institute (NCI)NIH
13,907 Previous Clinical Trials
41,012,117 Total Patients Enrolled
Julie SutcliffePrincipal InvestigatorUniversity of California, Davis
1 Previous Clinical Trials

Media Library

18F-αvβ6-BP Clinical Trial Eligibility Overview. Trial Name: NCT03164486 — Phase < 1
Pancreatic Cancer Research Study Groups: 18F-αvβ6-BP
Pancreatic Cancer Clinical Trial 2023: 18F-αvβ6-BP Highlights & Side Effects. Trial Name: NCT03164486 — Phase < 1
18F-αvβ6-BP 2023 Treatment Timeline for Medical Study. Trial Name: NCT03164486 — Phase < 1
~0 spots leftby Dec 2024
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