Overview

LCAR-B4822M-02 Cells in Treating Relapsed/Refractory (R/R) Multiple Myeloma

Status:
Unknown status
Trial end date:
2020-12-31
Target enrollment:
0
Participant gender:
All
Summary
This is a single arm, open-label, phase 1 study, to determine the safety and efficacy of LCAR-B4822M CAR-T cells in treating patients diagnosed with refractory/relapsed multiple myeloma (r/r MM).
Phase:
Phase 1
Accepts Healthy Volunteers?
No
Details
Lead Sponsor:
Second Affiliated Hospital of Xi'an Jiaotong University
Collaborator:
Nanjing Legend Biotech Co.
Criteria
Inclusion Criteria:

- Patients must have a confirmed prior diagnosis of active multiple myeloma as defined by
the updated IMWG criteria.

Patients with refractory multiple myeloma. Clear BCMA expression must be detected on
malignant plasma cells from either bone marrow or a plasmacytoma by flow cytometry or
immunohistochemistry.

Refractory diseaseļ¼š1) At least 3 prior regimens, which must at least have contained
bortezomi. or 2) other circumstances identified by clinical doctors.

Relapse criteria in NCCN clinical practice guidelines in Oncology: Multiple Myeloma
(2016.V2)

Exclusion Criteria:

- Women of child-bearing potential or who are pregnant or breastfeeding. Have any active
and uncontrolled infection: hepatitis B, hepatitis C, HIV, or other fatal viral and
bacterial infection.

Systemic corticosteroid steroid therapy of greater than 5 mg/day of prednisone or
equivalent dose of another corticosteroid are not allowed within 2 weeks prior to either
the required leukapheresis or the initiation of the conditioning chemotherapy regimen.

Patients with any uncontrolled intercurrent illness or serious uncontrolled medical
disorder.

Patients with CNS metastases or symptomatic CNS involvement (including cranial neuropathies
or mass lesions and spinal cord compression).

History of allogeneic stem cell transplantation. Have active acute or chronic
graft-versus-host-disease (GVHD), or require immunosuppressant medications for GVHD, within
6 months of enrollment.

Patients with active autoimmune skin diseases such as psoriasis or other active autoimmune
diseases such as rheumatoid arthritis.