drugset / Trial / NCT02718911
A Study of LY3022855 in Combination With Durvalumab or Tremelimumab in Participants With Advanced Solid Tumors
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
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| 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 |