drugset / Trial / NCT03652077

A Safety and Tolerability Study of INCAGN02390 in Select Advanced Malignancies

NCT03652077

Phase 1 Completed 40 enrolled Incyte Corporation
NaSingle-groupOpen-labelTreatment

Summary

The purpose of this study is to determine the safety, tolerability, and preliminary efficacy of INCAGN02390 in participants with select advanced malignancies.

Timeline

Start
2018-09-24
Primary completion
2021-08-18
Completion
2021-08-18

Drugs

EvaluationDrugModalityDoseRoute
Subject Verzistobart Monoclonal antibody