Phase 2b, Open-Label, Two-cohort Study of Subcutaneous Amivantamab in Combination with Lazertinib as First-Line Treatment, or Subcutaneous Amivantamab in Combination with Platinum-Based Chemotherapy as Second-line Treatment, for Common EGFR-Mutated Locally Advanced or Metastatic Non-Small Cell Lung Cancer
Sponsor: |
Janssen |
Enrolling: |
Male and Female Patients |
IRB Number: |
AAAV5314 |
U.S. Govt. ID: |
NCT06667076 |
Contact: |
Research Nurse Navigator: 212-342-5162 / cancerclinicaltrials@cumc.columbia.edu |
The purpose of this study is to understand more about the combination of amivantamab and lazertinib in non-small cell lung cancer (NSCLC) who have a specific mutation in the EGFR (epidermal growth factor receptor) gene and have not had prior treatment for their disease. The Food and Drug Administration (FDA) has not approved the combination of amivantamab subcutaneous (given as an injection under the skin) and lazertinib.
Investigator
Catherine Shu, MD
Are you 18 years or older? |
Yes |
No |
Are you currently enrolled in another investigational study? |
Yes |
No |
Do you agree to use sun protection until the last dose of study treatment? |
Yes |
No |