Melanoma Clinical Trials

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Correlation Between Early Interval 18F-Fluorodeoxyglucose Positron Emission Tomography/Computed Tomography (PET/CT) and Circulating Tumor DNA (ctDNA) in Advanced Melanoma Patients Treated With Immune Checkpoint Inhibitors

Status: Recruiting
Location: See location...
Intervention Type: Diagnostic test
Study Type: Observational
SUMMARY

The purpose of this research study is to determine if analysis of PET/CT scans and testing of blood samples in people with melanoma that has spread in their body can help researchers determine which patients are more or less likely to respond to immunotherapy and are more or less likely to have side effects. 24 participants will be enrolled and be on study until approximately 4 weeks after their first dose of Immune Checkpoint Inhibitor therapy.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
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• Willing to provide informed consent.

• Must have an advanced stage III or stage IV melanoma diagnosis for which treatment with ipilimumab, nivolumab, and/or pembrolizumab, either alone or in combination with other ICI therapy, is planned.

• Must be planning to participate in Signatera™ (ctDNA level) monitoring with standard of care laboratory testing routinely obtained for treatment with ICI therapy.

• Individuals at least 18 years of age.

• Women of childbearing potential must be willing to use effective contraception as discussed with their oncologist while participating in this study.

• Willing to comply with all study procedures and be available for the duration of the study.

Locations
United States
Wisconsin
University of Wisconsin Hospitals and Clinics (UWHC)
RECRUITING
Madison
Contact Information
Primary
Cancer Connect
clinicaltrials@cancer.wisc.edu
800-622-8922
Time Frame
Start Date: 2024-01-30
Estimated Completion Date: 2029-01
Participants
Target number of participants: 24
Treatments
Advanced Melanoma Patients with Immune Checkpoint Inhibitors
Related Therapeutic Areas
Sponsors
Leads: University of Wisconsin, Madison

This content was sourced from clinicaltrials.gov