CI

At a glance

ClinicalIndex Comparison Record
Phase 2Active· 53 enrolled
Drug / intervention
Chimeric Antigen Receptor T-Cell Therapy +4 morebiological
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT03277729
NCT03277729Phase 2Active

A Phase I/II Study to Evaluate the Safety of Cellular Immunotherapy Using Autologous T Cells Engineered to Express a CD20-Specific Chimeric Antigen Receptor for Patients With Relapsed or Refractory B Cell Non-Hodgkin Lymphomas

Fred Hutchinson Cancer Center·interventional·Posted Sep 11, 2017·Updated Jun 22, 2026

In Brief

A Phase 2 clinical trial evaluating Chimeric Antigen Receptor T-Cell Therapy, Cyclophosphamide, and 3 other interventions for Recurrent B-Cell Non-Hodgkin Lymphoma and 22 related conditions. Active but no longer recruiting, targeting 53 participants across 1 site.

Detailed Summary

The purpose of this research is to find the best dose of genetically modified T-cells, to study the safety of this treatment, and to see how well it works in treating patients with B cell non-Hodgkin lymphoma that has come back (relapsed) or did not respond to previous treatment (refractory).

Study Details

Timeline

Phase 2Active
2018201920202021202220232024202520262027202820292030203120322033203420352036203720382039
First PostedSep 11, 2017
Enrollment StartDec 5, 2017
Primary CompletionMar 29, 2024
Study CompletionMar 1, 2039
TodayJul 2, 2026
Enrollment to primary: 6.3 yearsPosted 8.8 years ago

Interventions

Chimeric Antigen Receptor T-Cell Therapybiological

Given CD20 CAR T cell IV

Cyclophosphamidedrug

Given IV

Laboratory Biomarker Analysisother

Correlative studies

Leukapheresisprocedure

Undergo leukapheresis

Fludarabine Phosphatedrug

Given IV