An Open-label Phase 1 Study of Oral ASP5878 at Single and Multiple Doses in Patients with Solid Tumors
Sponsor: |
Astellas |
Enrolling: |
Male and Female Patients |
IRB Number: |
AAAP3615 |
U.S. Govt. ID: |
NCT02038673 |
Contact: |
Emerson Lim: 212-305-1820 / el2342@columbia.edu |
The purpose of this research study is to confirm the safety of ASP5878. It is also intended to assess how the body reacts to ASP5878 after administration, how ASP5878 functions in the body, and the antitumor effect of the ASP5878. Participants in this study will have been diagnosed with urothelial carcinoma, hepatocellular carcinoma, or squamous cell lung carcinoma. Additionally, participants must test positive for a FGF/FGRF mutation/overexpression.
This study is closed
Investigator
Emerson Lim, MD
Do you have a confirmed diagnosis of urothelial carcinoma, hepatocellular carcinoma or squamous cell lung carcinoma? |
Yes |
No |