SynKIR-310 for Relapsed/Refractory B-NHL
Part of paid clinical trials in Denver, Colorado.
- Sponsor
- Verismo Therapeutics
- Study ID
- NCT06544265
- Phase
- PHASE1
- Status
- Recruiting
Conditions
- Aggressive B-Cell Non-Hodgkin Lymphoma
- B Cell Lymphoma
- DLBCL
- DLBCL (Diffuse Large B-Cell Lymphoma) Associated With Chronic Inflammation
- DLBCL - Diffuse Large B Cell Lymphoma
- Diffuse Large B Cell Lymphoma
- Epstein-Barr Virus Positive DLBCL, Nos
- Follicular Lymphoma
- Follicular Lymphoma Grade 3
- Follicular Lymphoma Grade 3B
- HGBL With MYC and BCL2 and/or BCL6 Rearrangements
- High Grade B-Cell Lymphoma, Not Otherwise Specified
- High-grade B-cell Lymphoma
- Indolent B-Cell Non-Hodgkin Lymphoma
- Large B-cell Lymphoma
- Mantle Cell Lymphoma
- Marginal Zone Lymphoma
- Marginal Zone Splenic Lymphoma
- NHL, Adult
- Non-hodgkin Lymphoma,B Cell
- Primary Mediastinal Large B-cell Lymphoma (PMBCL)
- Refractory Non-Hodgkin Lymphoma
- Relapsed Non-Hodgkin Lymphoma
- T-Cell/Histiocyte Rich Lymphoma
- Waldenstrom Macroglobulinaemia
- Waldenstrom Macroglobulinemia
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - N/A
- Healthy Volunteers
- Not accepted
Interventions
- SynKIR-310 — BIOLOGICALAutologous T Cells transduced with CD19 KIR-CAR
Study Details
This first-in-human (FIH) trial is designed to assess the safety, feasibility and preliminary efficacy of a single intravenous (IV) dose of SynKIR-310 administered to participants with relapsed/refractory B-NHL.
Key Dates
- Start date
- Nov 1, 2024
- Status verified
- Apr 2026
- Primary completion
- Sep 30, 2028
- Completion
- Dec 31, 2028
Study Design
- Enrollment
- 36 participants (estimated)
- Allocation
- NA
- Intervention model
- SINGLE_GROUP
- Primary purpose
- TREATMENT
Arms
- Experimental: SynKIR-310Single dose IV administration of SynKIR-310
Primary Outcome Measure
Evaluate the safety of SynKIR310 [ Time Frame: Up to 24 months ]
Central Contacts
- Physician Connect267-392-6847
Locations (5)
| Facility | City | State | ZIP | Site coordinators |
|---|---|---|---|---|
| Colorado Blood Cancer Institute, part of Sarah Cannon Cancer Institute | Denver | Colorado | 80218 | Michael T. Tees, MD (PRINCIPAL_INVESTIGATOR) |
| Winship Cancer Institute of Emory University | Atlanta | Georgia | 30322 | Edmund Waller, MD, PhD (PRINCIPAL_INVESTIGATOR) |
| The University of Kansas Cancer Center | Fairway | Kansas | 66205 | Joseph McGuirk, DO (PRINCIPAL_INVESTIGATOR) |
| Rutgers Cancer Institute | New Brunswick | New Jersey | 08902 | Matthew Matasar, MD (PRINCIPAL_INVESTIGATOR) |
| Abramson Cancer Center of the University of Pennsylvania | Philadelphia | Pennsylvania | 19104 | Stephen Schuster, MD (PRINCIPAL_INVESTIGATOR) |
Find similar trials in Denver, CO
By research site
Colorado Blood Cancer Institute, part of Sarah Cannon Cancer Institute· Denver, COWinship Cancer Institute of Emory University· Atlanta, GAThe University of Kansas Cancer Center· Fairway, KSRutgers Cancer Institute· New Brunswick, NJAbramson Cancer Center of the University of Pennsylvania· Philadelphia, PA
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