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A Study to Evaluate ABP 206 Compared With OPDIVO® (Nivolumab) in Subjects With Unresectable or Metastatic Melanoma

Melanoma Clinical Trial

Official title:
A Randomized, Double-Blind Study Evaluating the Efficacy, Safety, and Immunogenicity of ABP 206 Compared With OPDIVO® (Nivolumab) in Subjects With Treatment-Naïve Unresectable or Metastatic Melanoma

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

Clinical Trial Details
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
View Details
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