The purpose of this study is to assess the efficacy, safety, and immunogenicity of ABP
206 compared with Nivolumab in Subjects with Treatment-Naïve Unresectable or Metastatic
Melanoma.
Study sponsor and potential other locations can be found on ClinicalTrials.gov for NCT06054555.
Locations matching your search criteria
United States
Maryland
Baltimore
University of Maryland/Greenebaum Cancer CenterStatus: Active
Contact: Margaret Carder
Phone: 410-328-8611
Eligible subjects will be randomized (1:1) to receive investigational product (ABP 206 or
nivolumab).
All subjects will be treated until disease progression, unacceptable toxicity, or subject
withdrawal of consent for a maximum of 24 months of treatment.
The total duration of study participation for each subject will be approximately 26
months.
Lead OrganizationAmgen, Inc.