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 IMC-CS4 Monoclonal antibody 25 mg Intravenous
Subject IMC-CS4 Monoclonal antibody 50 mg Intravenous
Subject IMC-CS4 Monoclonal antibody 75 mg Intravenous
Subject IMC-CS4 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