drugset / Trial / NCT02791334

A Study of Anti-PD-L1 Checkpoint Antibody (LY3300054) Alone and in Combination in Participants With Advanced Refractory Solid Tumors

NCT02791334 ↗

Phase 1 Completed 164 enrolled Eli Lilly and Company
Non-randomizedParallel-groupOpen-labelTreatment

Summary

The main purpose of this study is to evaluate the safety and tolerability of anti-programmed cell death ligand 1 (PD-L1) checkpoint antibody LY3300054 in participants with advanced refractory solid tumors.

Timeline

Start
2016-06-29
Primary completion
2020-05-22
Completion
2024-06-27

Drugs

EvaluationDrugModalityDoseRoute
Subject Abemaciclib Small molecule — Oral
Subject LODAPOLIMAB Monoclonal antibody 700 mg Intravenous
Subject LY3321367 Monoclonal antibody 600 mg Intravenous
Subject Merestinib Small molecule — Oral
Subject Ramucirumab Monoclonal antibody — Intravenous