A Phase 2 Study to Evaluate the Safety and Efficacy of AB122 Monotherapy, AB154 in Combination With AB122, and AB154 in Combination With AB122 and AB928 in Front-Line, Non-Small Cell Lung Cancer
Sponsor: |
Arcus Biosciences, Inc. |
Enrolling: |
Male and Female Patients |
IRB Number: |
AAAS9418 |
U.S. Govt. ID: |
NCT04262856 |
Contact: |
Research Nurse Navigator: 212-342-5162 / cancerclinicaltrials@cumc.columbia.edu |
The purpose is to study the safety and the effect of AB122, AB154, and AB928 in participants with stage IV non-small cell lung cancer. Researchers will study the treatment response of AB122 alone as well as in combination with AB154 and AB928. There are three possible groups a participant can be randomly assigned to. Group 1 will include AB122 alone, Group 2 will include AB122 and AB154, and Group 3 will include a combination of AB122, AB154, and AB928.
This study is closed
Investigator
Brian Henick, MD
Are you at least 18 years of age? |
Yes |
No |
Do you have metastatic squamous or non-squamous non-small cell lung cancer (NSCLC)? |
Yes |
No |
Are you able to take oral medications? |
Yes |
No |