drugset / Trial / NCT03538028

A Safety and Tolerability Study of INCAGN02385 in Select Advanced Malignancies

NCT03538028

Phase 1 Completed 22 enrolled Incyte Corporation
NaSingle-groupOpen-labelTreatment

Summary

The purpose of this study is to determine the safety, tolerability, and preliminary efficacy of INCAGN02385 in participants with advanced malignancies.

Timeline

Start
2018-06-18
Primary completion
2020-10-07
Completion
2020-10-07

Drugs

EvaluationDrugModalityDoseRoute
Subject Tuparstobart Monoclonal antibody Intravenous