Clinical Trials Directory

Trials / Unknown

UnknownNCT05315778

Anti-BCMA CAR T-Cell Therapy for R/R ITP

Anti-BCMA CAR T-Cell Therapy for Relapsed/Refractory Immune Thrombocytopenia

Status
Unknown
Phase
Phase 2
Study type
Interventional
Enrollment
5 (estimated)
Sponsor
The First Affiliated Hospital of Soochow University · Academic / Other
Sex
All
Age
18 Years – 65 Years
Healthy volunteers
Not accepted

Summary

This is a prospective, single-center, open-label, single-arm study, to evaluate the efficacy and safety of Anti-BCMA chimeric antigen receptor T cell therapy(BCMA CAR-T)for patients with relapse/refractory Immune thrombocytopenia(R/R ITP).

Detailed description

Immune thrombocytopenia (ITP) is a disorder that can lead to easy or excessive bruising and bleeding. Approximately two-thirds of patients achieve remission after/during first-line therapies. However, the other part of patients could not achieve durable remission or even refractory to initial treatments. Those cases, known as relapse/refractory Immune thrombocytopenia (R/R ITP), undergo the heavy burden of disease which decreases the quality of life. Lots of pathogeneses take part in the occurrence of R/R ITP, and the most important one of them is antibody-mediated immune platelet destruction. As far as it is known,human platelet autoantibodies are mainly secreted by plasma cells, especially long-lived plasma cells. Researchers want to explore that can BCMA CAR-T help R/R ITP patients increase platelet count, reduce bleeding episodes and the dose of concomitant medications.

Conditions

Interventions

TypeNameDescription
BIOLOGICALautologous anti-BCMA chimeric antigen receptor T cellsLymphoadenodepletion chemotherapy with FC (fludarabine 30mg/ m2 for 3 consecutive days and cyclophosphamide 300mg/m2 for 3 consecutive days) will be given at day -5, -4 and -3 before CAR T-cells infusion. A total of 1.0-2.0×10e7/Kg autologous anti-BCMA CAR T-cells will be infused by dose-escalation after the lymphoadenodepletion chemotherapy. Dose of CAR T-cells are allowed to be adjusted according to the severity of cytokine release syndrome.

Timeline

Start date
2022-01-01
Primary completion
2022-12-31
Completion
2023-06-30
First posted
2022-04-07
Last updated
2022-04-07

Locations

1 site across 1 country: China

Source: ClinicalTrials.gov record NCT05315778. Inclusion in this directory is not an endorsement.