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Study details
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Anti-CD19 Chimeric Antigen Receptor T Cells for Treatment of Relapsed or Refractory Non-Hodgkin Lymphoma

C. Babis Andreadis
NCT IDNCT04545762ClinicalTrials.gov data as of Apr 2026
Phase

Phase 1

Target enrollment

36

Study length

about 6.1 years

Ages

18+

Locations

1 site in CA

About this study

This trial is testing a new treatment called anti-CD19 CAR-T cells to see if it's safe and can be used in people with relapsed or refractory non-Hodgkin lymphoma. The treatment involves genetically modifying T cells to target the CD19 protein on B cells.

Based on ClinicalTrials.gov records.

What participants do

  • 1.Receive anti-CD19 CAR-T cells
  • 2.Take Cyclophosphamide
  • 3.Take Fludarabine
PhasePhase 1
DrugCyclophosphamide
Routeinfusion
Primary goalProportion of participants who experience a dose-limiting toxicity (DLT) (Dose escalation)

Participation effort

Estimated from trial records. Details can vary by site.

Time + visits
Low15%
Logistics
Moderate50%

Logistics difficulty varies by site location and availability.

Trial highlights

Treatment details

Auto-extracted from trial records to preview treatments and outcomes.

Drug classes

cyclophosphamide (Alkylating chemotherapy; crosslinks DNA strands), fludarabine, cell therapy (Engineered T-cells that target specific cancer antigens)

Drug routes

infusion

Endpoints

Primary: Proportion of participants who experience a dose-limiting toxicity (DLT) (Dose escalation), Proportion of participants with treatment-emergent adverse events (AEs)

Secondary: Complete Response Rate, Median Overall Survival, Median Progression-free Survival (PFS), Median duration of response, Overall Response Rate (ORR), Partial Response Rate, Proportion of participants with CAR-T infusion related adverse events (Dose Escalation), Proportion of participants with delayed infusion due to study-related adverse events

Body systems

Oncology