A RANDOMIZED, PLACEBO-CONTROLLED, DOUBLE-BLIND STUDY OF ADJUVANT CEMIPLIMAB VERSUS PLACEBO AFTER SURGERY AND RADIATION THERAPY IN PATIENTS WITH HIGH-RISK CUTANEOUS SQUAMOUS CELL CARCINOMA
| Sponsor: |
Regeneron Pharmaceuticals, Inc. |
| Enrolling: |
Male and Female Patients |
| IRB Number: |
AAAS4125 |
| U.S. Govt. ID: |
NCT03969004 |
| Contact: |
Research Nurse Navigator: 212-342-5162 / cancerclinicaltrials@cumc.columbia.edu |
The purpose of this study is determine if cemiplimab will prevent Cutaneous Squamous Cell Cancer (CSCC) from returning after surgery and radiation.
This study is closed
Investigator
Shaheer Khan, DO
| Are you 18 years of age or older? |
Yes |
No |
| Were you diagnosed with Cutaneous Squamous Cell Cancer (CSCC)? |
Yes |
No |
| Are you able to understand and complete study-related questionnaires? |
Yes |
No |