drugset / Trial / NCT02718911

A Study of LY3022855 in Combination With Durvalumab or Tremelimumab in Participants With Advanced Solid Tumors

NCT02718911 ↗

Phase 1 Completed 72 enrolled Eli Lilly and Company AstraZeneca · collab
Non-randomizedSequentialOpen-labelTreatment

Summary

The main purpose of this study is to evaluate the safety of the colony-stimulating factor 1 receptor (CSF-1R) inhibitor LY3022855 in combination with durvalumab or tremelimumab in participants with advanced solid tumors.

Timeline

Start
2016-06-16
Primary completion
2018-12-14
Completion
2018-12-14

Drugs

EvaluationDrugModalityDoseRoute
Subject Durvalumab Monoclonal antibody 750 mg Intravenous
Subject LY3022855 Monoclonal antibody 25 mg Intravenous
Subject LY3022855 Monoclonal antibody 50 mg Intravenous
Subject LY3022855 Monoclonal antibody 75 mg Intravenous
Subject LY3022855 Monoclonal antibody 100 mg Intravenous
Subject Tremelimumab Monoclonal antibody 75 mg Intravenous
Subject Tremelimumab Monoclonal antibody 225 mg Intravenous
Subject Tremelimumab Monoclonal antibody 750 mg Intravenous

Indications