🏛️ Verified NIH Record • Updated 2026-07-30

A Study of Lazertinib With Subcutaneous Amivantamab Compared With Intravenous Amivantamab in Participants With Epidermal Growth Factor Receptor (EGFR)-Mutated Advanced or Metastatic Non-small Cell Lung Cancer (NCT05388669)

A Phase 3, Open-label, Randomized Study of Lazertinib With Subcutaneous Amivantamab Compared With Intravenous Amivantamab in Patients With EGFR-mutated Advanced or Metastatic Non-small Cell Lung Cancer After Progression on Osimertinib and Chemotherapy

🔵 Active, Not Recruiting Phase3 💊 Investigational Drug / Biologic Sponsor: Janssen Research & Development, LLC

🩺 Plain-English Summary (8th-Grade Level)

The purpose of the study is to simplify amivantamab intravenous administration and to reduce dose times, by assessing a new formulation of amivantamab, amivantamab subcutaneous and co-formulated with recombinant human hyaluronidase (SC-CF), for subcutaneous administration. This formulation has the potential to enhance both the patient and physician experience with amivantamab by providing easier and accelerated administration.

Who can join: Review the eligibility criteria below.

Location: City of Hope Duarte — Duarte, California

Age range: 18 Years

📋 "Do I Qualify?" — 1-Minute Self Screener

Instant Checklist

Full eligibility criteria are available on the official NIH protocol. View the criteria ↗

📍 All Participating Trial Locations (187 Sites)

Showing the first 25 of 187 sites.

  • City of Hope Duarte — Duarte, California
  • City of Hope Orange County Lennar Foundation Cancer Center — Irvine, California
  • City of Hope Long Beach Elm — Long Beach, California
  • National Jewish Health — Denver, Colorado
  • Baptist Lynn Cancer Institute — Boca Raton, Florida
  • Orlando Health — Orlando, Florida
  • University of Kansas — Kansas City, Kansas
  • University of Michigan — Ann Arbor, Michigan
  • Astera Cancer Care — East Brunswick, New Jersey
  • Rutgers Cancer Institute of New Jersey — New Brunswick, New Jersey
  • NYU Langone Health Laura and Isaac Perlmutter Cancer Center — New York, New York
  • Montefiore Medical Center — The Bronx, New York
  • Providence Portland Medical Center — Portland, Oregon
  • Providence Oncology and Hematology Care Clinic Westside — Portland, Oregon
  • University of Pennsylvania Division of Hematology Oncology Perelman Center for Advanced Medicine — Philadelphia, Pennsylvania
  • Medical University of South Carolina — Charleston, South Carolina
  • Virginia Cancer Specialists — Fairfax, Virginia
  • CEMIC (Centro de Educación Médica e Investigaciones Clínicas) — Buenos Aires,
  • Centro Oncológico Korben — Buenos Aires,
  • IADT Instituto Argentino de Diagnostico y Tratamiento — CABA,
  • Cemaic Centro Privado de Especialidades Medicas Ambulatorias e Investigacion Clinica — Córdoba,
  • Sanatorio Allende — Córdoba,
  • Clínica Viedma — Viedma,
  • Cancer Research SA — Adelaide,
  • Chris O'Brien Lifehouse — Camperdown,

📞 Contact the Study Coordinator

Phone: (800) 826-4673

Coordinator details come directly from the registered NIH protocol. Confirm the study is still recruiting before traveling.

💰 Cost, Insurance & Patient Rights

  • 100% Free Items: The investigational treatment and protocol-required procedures are supplied at zero cost by the sponsor.
  • Routine Patient Care: Under federal law (ACA § 2709) and many state statutes, routine care costs are covered during participation.
  • Voluntary Participation: You may withdraw at any time without affecting your standard medical care.

💡 How to Participate

  1. Check the checklist above to see if you may qualify.
  2. Contact the study coordinator using the phone/email above.
  3. Ask about the visit schedule, what is covered at no cost, and any travel support.
  4. Confirm with your own doctor before making a decision.
🏛️ View Official NIH Record ↗