Condition: Advanced Melanoma and Normal or Impaired · Advanced Melanoma · Sponsor: Yale University
This study is a first-in-human, open-label, nonrandomized, single center Phase 1 dose-escalation study to assess the safety, pharmacokinetics, pharmacodynamics, immunogenicity, and preliminary antitumor activity of AB821 monotherapy given every 2 weeks (Q2W) or every 3 weeks (Q3W) in participants with recurrent locally advanced or metastatic melanoma and other immune-responsive solid tumors. Immune-responsive solid tumors are defined as those for which immune checkpoint inhibitors form part of the standard-of-care therapy.
This description comes directly from the study's public registry record.
Stephanie Ladd · 203-785-5702 · stephanie.ladd@yale.edu
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| Yale University | New Haven, Connecticut, United States | Recruiting |
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Source record: clinicaltrials.gov/study/NCT07027488