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
π©Ί 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
π§ͺ Interventions in This Study
π "Do I Qualify?" β 1-Minute Self Screener
Instant ChecklistFull eligibility criteria are available on the official NIH protocol. View the criteria β
π 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,
π 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.
π° 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.
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- THIO Sequenced With Cemiplimab in Advanced NSCLC β Birmingham, Alabama
- Oleclumab (MEDI9447) Epidermal Growth Factor Receptor Mutant (EGFRm) Non-small Cell Lung Cancer (NSCLC) Novel Combination Study β La Jolla, California
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π‘ How to Participate
- Check the checklist above to see if you may qualify.
- Contact the study coordinator using the phone/email above.
- Ask about the visit schedule, what is covered at no cost, and any travel support.
- Confirm with your own doctor before making a decision.