A Phase 1/2, open-label, single-arm, dose-escalation and dose-expansion study of the safety, tolerability, pharmacokinetic, and antitumor activity of E-602 as a single agent and in combination with Cemiplimab in patients with advanced cancers
Sponsor: |
Palleon Pharmaceuticals |
Enrolling: |
Male and Female Patients |
IRB Number: |
AAAU1677 |
U.S. Govt. ID: |
NCT05259696 |
Contact: |
Research Nurse Navigator: 212-342-5162 / cancerclinicaltrials@cumc.columbia.edu |
The purpose of this study is to test the safety of the study drug, E-602, at different dose levels both alone (monotherapy) and in combination with Cemiplimab (also known as Libtayo). Cemiplimab is FDA-approved for the treatment of some cancers, but not all of the cancers in this study. E-602 has not been approved by the United States Food and Drug Administration (FDA). This study is the first time that E-602 will be administered to participants. The study will also inform on what effects, both good and bad, E-602 alone and in combination with Cemiplimab have on participants with advanced cancer. Cancers include: breast cancer, colon and rectal cancer, esophageal cancer, head and neck/oral cancer, lung cancer, melanoma, pancreatic cancer, and ovarian cancer.
This study is closed
Investigator
Brian Henick, MD
Are you at least 18 years old? |
Yes |
No |
Have you been diagnosed with advanced cancer? |
Yes |
No |