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Clinical Trial Summary

The purpose of this study is to evaluate the efficacy and safety of ANV419 monotherapy or the combination of ANV419 with anti-PD1 antibody or with anti-CTLA4 antibody in adult participants with advanced (unresectable or metastatic) cutaneous melanoma.


Clinical Trial Description

The purpose of this multi-site, open-label, randomized, parallel arm, Phase 1/2 adaptive study is to evaluate the efficacy and safety of ANV419 as a monotherapy and in combination with anti-PD1 antibody or anti-CTLA4 antibody in patients aged 18 years or older with advanced Cutaneous Melanoma who have previously been treated with an anti-PD-1/anti-PD-L1 antibody. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05578872
Study type Interventional
Source Anaveon AG
Contact Claudia Schusterbauer, MD
Phone +41615218383
Email anaveonclinicaltrials@anaveon.com
Status Recruiting
Phase Phase 1/Phase 2
Start date December 16, 2022
Completion date December 2024

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