drugset / Trial / NCT03343613

A Study of LY3381916 Alone or in Combination With LY3300054 in Participants With Solid Tumors

NCT03343613

Phase 1 Terminated 60 enrolled Eli Lilly and Company
Non-randomizedSingle-groupOpen-labelTreatment

Summary

The purpose of this study is to evaluate the safety of the study drug LY3381916 administered alone or in combination with anti-programmed cell death ligand 1 (PD-L1) checkpoint antibody (LY3300054).

Timeline

Start
2017-11-17
Primary completion
2020-02-07
Completion
2020-05-04

Drugs

EvaluationDrugModalityDoseRoute
Subject LODAPOLIMAB Monoclonal antibody Intravenous
Subject LY3381916 Small molecule Oral