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

Contact:

NCT Number:

Protocol:

AAAV5314

Study Status:

Active/Enrolling

Population:

Adult

Phase:

II

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.

Are you Eligible? (Inclusion Criteria)

  • must be 18 years old or older - must not be currently enrolled in another investigational study - must agree to use sun protection until the last dose of study treatment

Specialty Area(s)

Lung cancer, Immunotherapy

Principal Investigator

Profile Headshot
  • Clinical Director, Thoracic Medical Oncology Service

Trial Location(s)

CUIMC/Herbert Irving Pavilion
161 Fort Washington Avenue
New York, NY 10032