← Eichor
Study identifier: NCT06199713 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

Correlating Early FDG PET/CT and ctDNA in Immune Checkpoint Inhibitor (ICI)-Treated Melanoma Patients

Condition: Melanoma · Melanoma Stage III · Melanoma Stage IV  ·  Sponsor: University of Wisconsin, Madison

PhaseN/A
Planned participants24
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNo

About this study

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.

This description comes directly from the study's public registry record.

Talk to the study team

Cancer Connect  ·  800-622-8922  ·  clinicaltrials@cancer.wisc.edu

Always discuss trial participation with your own doctor first.

Locations (1)

University of Wisconsin Hospitals and Clinics (UWHC)Madison, Wisconsin, United StatesRecruiting

Follow this study

Get one email when the public record changes — results posted, or the study's status changes. Nothing else, ever.

We email about this public record only. Unsubscribe anytime with one click. Never medical advice.

Is this your study? This page was generated automatically from the public registry record. Sponsors can claim it — free — to add branding and verified contact routing. Claim this page →

This page is independently generated by Eichor from the public ClinicalTrials.gov record and re-synced daily. It is not the sponsor's official website unless claimed. Nothing here is medical advice; eligibility is always determined by the study team — talk to your own doctor first.

Source record: clinicaltrials.gov/study/NCT06199713