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Clinical Trial Summary

The purpose of this study is to determine the safety, tolerability, efficacy, PK and pharmacodynamics of INCAGN01876 when given in combination with retifanlimab. The study will consist of 2 parts: a safety lead-in part (Part 1) followed by a dose expansion part (Part 2).


Clinical Trial Description

The purpose of this study is to determine the safety, tolerability, efficacy, PK and pharmacodynamics of INCAGN01876 when given in combination with retifanlimab in participants with GITR expression in recurrent or metastatic HNSCC who have progressed on or after prior systemic therapy including anti-PD-(L)1 therapy. The study will consist of 2 parts: a safety lead-in part (Part 1) followed by a dose expansion part (Part 2) ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05359692
Study type Interventional
Source Incyte Corporation
Contact
Status Withdrawn
Phase Phase 2
Start date March 1, 2023
Completion date January 11, 2025

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