drugset / Trial / NCT03752177

A Study of LY3415244 in Participants With Advanced Solid Tumors

NCT03752177 ↗

Phase 1 Terminated 12 enrolled Eli Lilly and Company
Non-randomizedSingle-groupOpen-labelTreatment

Summary

The goal of this study is to evaluate the safety of LY3415244, a PD-L1/TIM-3 bispecific antibody, administered as monotherapy to participants with advanced solid tumors.

Timeline

Start
2018-11-22
Primary completion
2019-10-09
Completion
2019-10-09

Outcome

Outcome not reported

Stopped: “The study was terminated during dose escalation after a determination was made that the risk:benefit ratio no longer favored continued evaluation.”

Drugs

EvaluationDrugModalityDoseRoute
Subject LY3415244 Unknown 3 mg Intravenous
Subject LY3415244 Unknown 10 mg Intravenous
Subject LY3415244 Unknown 30 mg Intravenous
Subject LY3415244 Unknown 70 mg Intravenous

Indications