Clinical Trials Directory

Trials / Unknown

UnknownNCT03468153

Dual Specificity CD19 and CD22 CAR-T Cell Immunotherapy for CD19+CD22+ Relapsed and Refractory Lymphoma

The Safety and Efficacy of Dual Specificity CD19 and CD22 CAR-T Cell Immunotherapy for CD19+CD22+ Relapsed and Refractory Lymphoma

Status
Unknown
Phase
Phase 1 / Phase 2
Study type
Interventional
Enrollment
10 (estimated)
Sponsor
Ruijin Hospital · Academic / Other
Sex
All
Age
18 Years – 65 Years
Healthy volunteers
Not accepted

Summary

Patients with relapsed or refractory lymphoma often develop resistance to chemotherapy. Chimeric antigen receptor-modified T cell (CART) therapy showed promising effect in B-cell malignancies these years. CD19 and CD22 are proteins expressed on the surface of the lymphoma cells in patients with CD19+CD22+ lymphoma. The CAR enables the T-cells to recognize and kill the tumor cell through recognition of CD19 and CD22. This is a phase 2 trial to study the safety and efficacy of dual specificity CD19 and CD22 CAR-T cell immunotherapy for CD19+CD22+ relapsed and refractory lymphoma.

Conditions

Interventions

TypeNameDescription
BIOLOGICALDual Specificity CD19 and CD22 CAR-T Cell ImmunotherapyPatient-derived dual specificity CD19 and CD22 CAR-T Cells

Timeline

Start date
2018-01-01
Primary completion
2019-01-01
Completion
2020-01-01
First posted
2018-03-16
Last updated
2018-03-20

Locations

1 site across 1 country: China

Source: ClinicalTrials.gov record NCT03468153. Inclusion in this directory is not an endorsement.