External Beam Radiotherapy Followed by Bispecific Antibody Therapy for Relapsed/Refractory DLBCL
Part of paid clinical trials in Salt Lake City, Utah.
- Sponsor
- University of Utah
- Study ID
- NCT07528352
- Phase
- PHASE1
- Status
- Recruiting
Conditions
- Diffuse Large B Cell Lymphoma
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - N/A
- Healthy Volunteers
- Not accepted
Interventions
- Epcoritamab — DRUGEpcoritamab will be administered per standard of care.
- Glofitamab — DRUGGlofitamab will be administered per standard of care.
- External Beam Radiation Therapy — RADIATIONParticipants will receive radiation therapy for 5 fractions completed on sequential days.
Study Details
The purpose of this clinical trial is to assess the safety and tolerability of ration therapy followed by receiving epcoritamab or glofitamab in patients with relapsed/refractory diffuse large B-cell lymphoma.
Key Dates
- Start date
- Jun 1, 2026
- Status verified
- Jun 2026
- Primary completion
- Jun 30, 2030
- Completion
- Jun 30, 2031
Study Design
- Enrollment
- 12 participants (estimated)
- Allocation
- NA
- Intervention model
- SINGLE_GROUP
- Primary purpose
- TREATMENT
Arms
- Experimental: Radiation followed by bispecific antibody therapyThis study will investigate the safety and tolerability of 5 days of radiation therapy followed directly by a bispecific antibody therapy (Epcoritamab or Glofitamab).
Primary Outcome Measure
The rate of CRS and ICANS adverse events as measured by ASTCT criteria attributed to RT and epcoritamab or glofitamab therapy. [ Time Frame: 18 months ]
Central Contacts
- David Samuel801-587-4713
- Allison Bock, MD801-585-0255
Locations (1)
| Facility | City | State | ZIP | Site coordinators |
|---|---|---|---|---|
| Huntsman Cancer Institute at University of Utah | Salt Lake City | Utah | 84112 | Allison Bock, MD (PRINCIPAL_INVESTIGATOR) |
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