A Study of JNJ-90301900 in Combination With Chemoradiation Followed by Consolidation Immunotherapy for Non-Small Cell Lung Cancer (NSCLC) (NCT06667908)
A Phase 2, Randomized, Open-Label, Active-Controlled Study of JNJ-90301900 in Combination With Chemoradiation Followed by Durvalumab in Locally Advanced and Unresectable Stage III NSCLC
π©Ί Plain-English Summary (8th-Grade Level)
The purpose of this study is to determine whether JNJ-90301900 added to concurrent platinum-based doublet chemotherapy with radiation therapy (cCRT) followed by consolidation immunotherapy (cIT) can improve objective response rate (ORR; that is percentage of participants whose best response is complete response or partial response during the study) in participants with locally advanced and unresectable stage III non-small cell lung cancer.
Who can join: Review the eligibility criteria below.
Location: Moores Cancer Center at UC San Diego Health β La Jolla, 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 (43 Sites)
Showing the first 25 of 43 sites.
- Moores Cancer Center at UC San Diego Health β La Jolla, California
- University of Connecticut Health Center β Farmington, Connecticut
- Yale University β New Haven, Connecticut
- University of Miami β Miami, Florida
- Orlando Health Cancer Institute β Orlando, Florida
- Emory University Winship Cancer Institute β Atlanta, Georgia
- Beth Israel Deaconess Medical Center β Boston, Massachusetts
- Washington University in St Louis β St Louis, Missouri
- Rutgers Cancer Institute of New Jersey β New Brunswick, New Jersey
- NYU Langone Health β New York, New York
- Memorial Sloan Kettering Cancer Center β New York, New York
- University of North Carolina at Chapel Hill β Chapel Hill, North Carolina
- FirstHealth of the Carolinas β Pinehurst, North Carolina
- University Hospitals Cleveland Medical Center β Cleveland, Ohio
- Oregon Health And Science University β Portland, Oregon
- University of Pennsylvania β Philadelphia, Pennsylvania
- MD Anderson Cancer Center β Houston, Texas
- University of Vermont Medical Center β Burlington, Vermont
- Royal Brisbane and Women's Hospital β Herston,
- Sir Charles Gairdner Hospital β Nedlands,
- Macquarie University β North Ryde,
- Royal Melbourne Hospital β Parkville,
- Fundacao Pio XII β Barretos,
- Sociedade Beneficente de Senhoras Hospital Sirio Libanes β SΓ£o Paulo,
- Sociedade Beneficente Israelita Brasileira Hospital Albert Einstein β SΓ£o Paulo,
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.