πŸ›οΈ Verified NIH Record β€’ Updated 2026-08-27

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

🟒 Recruiting Phase2 πŸ’Š Investigational Drug / Biologic Sponsor: Johnson & Johnson Enterprise Innovation Inc.

🩺 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

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 (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,

πŸ“ž 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.

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†—