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Clinical Trial Summary

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.


Clinical Trial Description

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. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT06054555
Study type Interventional
Source Amgen
Contact Amgen Call Center
Phone 1-800-772-6436
Email medinfo@amgen.com
Status Recruiting
Phase Phase 3
Start date November 2, 2023
Completion date January 25, 2027

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