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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

What this study is about

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.

Simplified from trial records by PatientMatch.

What you may be asked to do

  • 1.Receive anti-CD19 CAR-T cells
  • 2.Take Cyclophosphamide
  • 3.Take Fludarabine

Participation Burden

What's physically and logistically required of participants.

Logistics & Travel
In-person visits

Requires travel to a study site

Physical Intervention
Injection / IV

How treatment is administered

Treatment Assignment
All receive treatment

Everyone gets the investigational treatment.

Extracted study details

Pulled from the trial record to show what is being tested and what the study is measuring.

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