A Study of Neoadjuvant Amivantamab With Either Lazertinib or Chemotherapy in Participants With Resectable EGFR-Mutated NSCLC (NCT07586202)
A Phase 2 Study Evaluating the Safety and Efficacy of Neoadjuvant Amivantamab in Combination With Lazertinib or Chemotherapy in Resectable EGFR-Mutated Non-Small Cell Lung Cancer
π©Ί Plain-English Summary (8th-Grade Level)
The purpose of this study is to assess the ability to slow down or stop the growth of cancer with amivantamab combined with either lazertinib or chemotherapy (carboplatin and pemetrexed) in participants with resectable, epidermal growth factor receptor (EGFR) mutated, Stage II-IIIB non-small cell lung cancer (NSCLC). NSCLC is the most common type of lung cancer. NSCLC may occur due to mutations (changes) in many genes, including EGFR.
Who can join: Review the eligibility criteria below.
Location: City of Hope 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 (20 Sites)
- City of Hope β Duarte, California
- City of Hope 1 β Irvine, California
- Providence Cancer Center β Portland, Oregon
- Providence Oncology and Hematology Care Clinic Westside β Portland, Oregon
- Princess Margaret Hospital β Toronto, Ontario
- Sichuan Cancer Hospital β Cheng Du Shi,
- West China Hospital Sichuan University β Chengdu,
- Guangdong Provincial People's Hospital β Guangzhou,
- Shandong Cancer Hospital β Jinan,
- Tianjin Chest Hospital β Tianjin,
- Kyungpook National University Chilgok Hospital β Buk Gu,
- Pusan National University Hospital β Busan,
- Samsung Medical Center β Seoul,
- Korea University Guro Hospital β Seoul,
- Hosp. Gral. Univ. Dr. Balmis β Alicante,
- Hosp. Gral. Univ. Gregorio Maranon β Madrid,
- Taichung Veterans General Hospital β Taichung,
- Chi Mei Medical Center Liouying Branch β Tainan,
- Taipei Medical University Hospital β Taipei,
- NTU Biomedical Park Hospital β Zhubei,
π Contact the Study Coordinator
Phone: (844) 434-4210
Email: Participate-In-This-Study1@its.jnj.com
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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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.