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
Study of E-602 Alone or in Combination with Libtayo (Cemiplimab) in Patients with Advanced Cancer
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
Additional Study Information: 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
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Are you at least 18 years old? Yes No
Have you been diagnosed with advanced cancer? Yes No
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For more information, please contact:
Research Nurse Navigator
cancerclinicaltrials@cumc.columbia.edu
212-342-5162