Prizloncabtagene Autoleucel (Prizlon-cel) for the Treatment of Relapsed or Refractory Large B-cell Lymphoma Post FDA Approved CAR T-cell Therapy
Part of paid clinical trials in Gilbert, Arizona.
- Sponsor
- AbelZeta Inc.
- Study ID
- NCT07875413
- Phase
- PHASE2
- Status
- Not Yet Recruiting
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Conditions
- Diffuse Large B Cell Lymphoma (DLBCL)
- FL
- HGBL
- HGBL With MYC and BCL2 and/or BCL6 Rearrangements
- High Grade B Cell Lymphoma
- LBCL
- Large B Cell Lymphoma
- PMBCL
- Primary Mediastinal B Cell Lymphoma
- Relapse Diffuse Large B Cell Lymphoma
- Transformed Follicular Lymphoma (TFL)
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - N/A
- Healthy Volunteers
- Not accepted
Interventions
- Prizloncabtagene Autoleucel — BIOLOGICALAn Autologous anti-CD19/CD20 chimeric antigen receptor T-cell therapy
Study Details
This Phase 2, multicenter, open-label study will evaluate the safety and efficacy of a single infusion of Prizloncel, an anti-CD19/CD20 chimeric antigen receptor T cells following lymphodepleting chemotherapy in participants with relapsed/refractory (r/r) diffuse large B-cell lymphoma post FDA approved, commercially available CAR T-cell therapy Approximately 50 participants will undergo leukapheresis, lymphodepletion with fludarabine and cyclophosphamide, and infusion of Prizlon-cel. Participants will be followed for 24 months (approximately 2 years) to evaluate efficacy, safety, CAR T-cell persistence, pharmacokinetics/pharmacodynamics, and biomarkers. Long-term safety follow-up for gene therapy-related events will continue for up to 15 years following CAR T-cell infusion.
Key Dates
- First listed
- Oct 15, 2026
- Start date
- May 31, 2027
- Status verified
- Oct 2026
- Primary completion
- Jun 30, 2029
- Completion
- Dec 31, 2030
Study Design
- Enrollment
- 55 participants (estimated)
- Allocation
- NA
- Intervention model
- SINGLE_GROUP
- Primary purpose
- TREATMENT
Arms
- Experimental: Prizlon-celParticipants will receive: • Leukapheresis • Fludarabine • Cyclophosphamide • Single intravenous infusion of Prizlon-cel.
Primary Outcome Measure
Overall Response Rate (ORR) [ Time Frame: Through Month 24 ]
Central Contacts
- Kirstin Liechty, Head of Clinical Operations267-566-6081
Locations (2)
| Facility | City | State | ZIP | Site coordinators |
|---|---|---|---|---|
| Research Site | Gilbert | Arizona | 85234 | - |
| Research Site | La Jolla | California | 92037 | - |
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