A Study to Evaluate the Safety and Efficacy of Glofitamab in Combination With Rituximab (R) Plus Cyclophosphamide, Doxorubicin, Vincristine, and Prednisone (CHOP) in Circulating Tumor (ct)DNA High-Risk Patients With Untreated Diffuse Large B-Cell Lymphoma (NCT04980222)
A Phase II Study Evaluating the Safety and Efficacy of Glofitamab in Combination With Rituximab (R) Plus Cyclophosphamide, Doxorubicin, Vincristine, and Prednisone (CHOP) in Circulating Tumor (ct)DNA High-Risk Patients With Untreated Diffuse Large B-Cell Lymphoma
🩺 Plain-English Summary (8th-Grade Level)
This Phase II, open-label, multicenter study will evaluate the safety, efficacy, and pharmacokinetics of glofitamab in combination with rituximab in combination with cyclophosphamide, doxorubicin, vincristine, and prednisone (R-CHOP) in individuals with circulating tumor DNA (ctDNA) high-risk diffuse large B-cell lymphoma (DLBCL), as the first line of treatment.
Who can join: Review the eligibility criteria below.
Location: City of Hope Comprehensive Cancer Center — Duarte, California
Age range: 18 Years
🧪 Interventions in This Study
📋 "Do I Qualify?" — 1-Minute Self Screener
Instant ChecklistFull eligibility criteria are available on the official NIH protocol. View the criteria ↗
📍 All Participating Trial Locations (20 Sites)
- City of Hope Comprehensive Cancer Center — Duarte, California
- Stanford Cancer Center — Stanford, California
- Stanford Cancer Institute Inpatient Investigational Pharmacy — Stanford, California
- University of Iowa — Iowa City, Iowa
- University of Michigan Health System — Ann Arbor, Michigan
- Washington University; Wash Uni. Sch. Of Med — St Louis, Missouri
- Memorial Sloan Kettering Bergen — Montvale, New Jersey
- Memorial Sloan Kettering Cancer Center at Westchester — East White Plains, New York
- Memorial Sloan Kettering Cancer Center — New York, New York
- Baylor University Medical Center — Dallas, Texas
- Aarhus Universitetshospital Skejby — Aarhus N,
- Hopital Henri Mondor — Créteil,
- Centre Henri Becquerel — Rouen,
- Universitair Medisch Centrum Groningen — Groningen,
- Uniwersyteckie Centrum Kliniczne, Klinika Hematologii i Transplantologii — Gdansk,
- Uniwersytecki Szpital Kliniczny; Klinika Hematologii, Nowotworów Krwi i Transplantacji Szpiku — Wroclaw,
- Hospital Clinic i Provincial de Barcelona — Barcelona, BARCELONA
- Hospital General Universitario Gregorio Marañon — Madrid, Madrid
- Hospital Univ. 12 de Octubre; Servicio de Hematologia — Madrid, Madrid
- Hospital Clinico Universitario de Salamanca — Salamanca, SALAMANCA
📞 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.
💰 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 § 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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💡 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.