πŸ›οΈ Verified NIH Record β€’ Updated 2026-07-02

A Study of Combination Amivantamab and Carboplatin-Pemetrexed Therapy, Compared With Carboplatin-Pemetrexed, in Participants With Advanced or Metastatic Non-Small Cell Lung Cancer Characterized by Epidermal Growth Factor Receptor (EGFR) Exon 20 Insertions (NCT04538664)

A Randomized, Open-label Phase 3 Study of Combination Amivantamab and Carboplatin-Pemetrexed Therapy, Compared With Carboplatin-Pemetrexed, in Patients With EGFR Exon 20ins Mutated Locally Advanced or Metastatic Non-Small Cell Lung Cancer

πŸ”΅ Active, Not Recruiting Phase3 πŸ’Š Investigational Drug / Biologic Sponsor: Janssen Research & Development, LLC

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

The purpose of this study is to compare the efficacy, as demonstrated by progression-free survival (PFS), in participants treated with amivantamab in combination with chemotherapy, versus chemotherapy alone in participants with locally advanced or metastatic non-small cell lung cancer (NSCLC) characterized by EGFR Exon 20ins mutations.

Who can join: Review the eligibility criteria below.

Location: City of Hope 2 β€” Duarte, California

Age range: 18 Years

πŸ“‹ "Do I Qualify?" β€” 1-Minute Self Screener

Instant Checklist

Full eligibility criteria are available on the official NIH protocol. View the criteria β†—

πŸ“ All Participating Trial Locations (232 Sites)

Showing the first 25 of 232 sites.

  • City of Hope 2 β€” Duarte, California
  • University of California Irvine β€” Orange, California
  • UCLA β€” Santa Monica, California
  • Georgetown University Hospital β€” Washington D.C., District of Columbia
  • H. Lee Moffitt Cancer & Research Institute β€” Tampa, Florida
  • University Cancer And Blood Center LLC β€” Athens, Georgia
  • Henry Ford Hospital β€” Detroit, Michigan
  • Washington University Medical Center β€” St Louis, Missouri
  • Regional Cancer Care Associates LLC β€” East Brunswick, New Jersey
  • Langone Health at NYC University, NYU School of Medicine β€” New York, New York
  • Columbia University Medical Center β€” New York, New York
  • Providence Portland Medical Center β€” Portland, Oregon
  • Sanford Health β€” Sioux Falls, South Dakota
  • Texas Oncology Pa β€” Tyler, Texas
  • Utah Cancer Specialists β€” Salt Lake City, Utah
  • Virginia Cancer Specialists β€” Fairfax, Virginia
  • Blue Ridge Cancer Care β€” Salem, Virginia
  • Chris O'Brien Lifehouse β€” Camperdown,
  • St George Hospital β€” Kogarah,
  • Cabrini Medical Centre β€” Malvern,
  • Sir Charles Gairdner Hospital β€” Nedlands,
  • UZ Leuven β€” Leuven,
  • Algemeen Ziekenhuis Delta β€” Roeselare,
  • CHU UCL Namur - Site Godinne β€” Yvoir,
  • Fundacao Pio XII β€” Barretos,

πŸ“ž 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.

πŸ’° 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 Β§ 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.

πŸ’‘ 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.
πŸ›οΈ View Official NIH Record β†—