Phase 2 trial of enfortumab vedotin plus pembrolizumab with selective bladder sparing for treatment of muscle-invasive urothelial cancer of the bladder: HCRN GU22-598
| Sponsor: |
Astellas Pharma, Hoosier Cancer Research Network, & Merck |
| Enrolling: |
Male and Female Patients |
| IRB Number: |
AAAV9307 |
| U.S. Govt. ID: |
NCT06809140 |
| Contact: |
Alexander Wei: / cancerclinicaltrials@cumc.columbia.edu |
The purpose of this study is to see if the combination of enfortumab vedotin and pembrolizumab leads to no detectable cancer on early assessments of the bladder after initial treatment. We are asking you to take part in this research study because you have muscle-invasive bladder cancer. This combination of enfortumab vedotin and pembrolizumab has been tested in people and is approved by the U.S. Food and Drug Administration (FDA) to treat patients with bladder cancer that has spread outside of the bladder (also known as metastatic bladder cancer).
Investigator
Alexander Wei, MD
| Do you have muscle-invasive bladder cancer? |
Yes |
No |