Condition: Metastatic Melanoma · Sponsor: Duke University
The primary objective of this study is to determine the safety and feasibility of administering an IL-17A (human IgG1κ) monoclonal antibody, (Secukinumab, Cosentyx®) to participants with metastatic melanoma who have previously received immune checkpoint inhibitor (ICI) therapy, experienced an immune related adverse event (colitis, hepatitis, skin rash, psoriatic arthritis) to ICI, and are re-initiating ICI therapy.
This description comes directly from the study's public registry record.
April Salama, MD · +1 919 681 9507 · april.salama@duke.edu
Emily Bolch · emily.bolch@duke.edu
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| Duke University Health System | Durham, North Carolina, United States | Recruiting |
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Source record: clinicaltrials.gov/study/NCT07237594