Study to Evaluate the Safety and Efficacy of IM19 CAR-T Cells in Patients With Relapsed and Refractory (R/R) Mantle Cell Lymphoma

Beijing Immunochina Medical Science & Technology

Status and phase

Unknown

Phase 2

Phase 1

Conditions

Neoplasms by Histologic Type

Lymphoma, Mantle-Cell

Neoplasms

Lymphoma

Lymphoproliferative Disorders

Treatments

Biological: IM19 CAR-T cells

Drug: Cyclophosphamide

Drug: Fludarabine

Study type

Interventional

Funder types

Industry

Identifiers

NCT05155215

SD46

Details and patient eligibility

About

This is a phase I/II, open-label, multicenter study to assess the efficacy and safety of IM19 CAR-T cells in adult R/R Mantle Cell Lymphoma subjects

Enrollment

68 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

Subjects with relapsed or refractory mantle cell lymphoma, diagnosed as CD19 positive by cytology or histology；
Subjects have measurable positive lesion according to Lugano Classification;
≥ 18 years old;
Expected survival is greater than 3 months；
Eastern Cooperative Oncology Group (ECOG) performance status of 0 or 1;
The toxicity caused by the previous treatment has stabilized or recovered to ≤1 level (except for the case where the investigator judges that it has no clinical significance);
Women of childbearing age who had a negative blood pregnancy test before the start of the trial and agreed to take effective contraceptive measures during the trial period until the last follow-up; male subjects with fertility partners agreed to take effective contraceptive measures during the trial period until the last follow-up;
Adequate organ function;
Adequate vascular access for leukapheresis procedure;
Volunteer to participate in this trial and sign on the informed consent.

Exclusion criteria

Central nervous system (CNS) involvement by lymphoma;
Received allo-hematopoietic stem cell transplantation or organ transplantation therapy previously；
Subjects with cardiac atrial or cardiac ventricular lymphoma involvement；
Serous effusion with symptoms of compression;
History of autoimmune disease (eg Crohn's disease, rheumatoid arthritis, systemic lupus) within the last 2 years;
Presence of acute or chronic graft-versus-host disease (GVHD);
Use prohibited drugs or treatments within a specified period of time before cell collection；
Received anti-CD19 target therapy (unless the CD19 target test is still positive);
Received CAR-T cell therapy;
Received the study drug within 4 weeks before cell collection. However, if the trial treatment is invalid or the disease progresses, and at least 5 half-lives have passed before the cell collection, it is allowed to enter the group;
Received radiotherapy within 6 weeks prior to cell collection, including large bone marrow areas such as the sternum or pelvis. Subjects who have progressed in the radiotherapy site or have PET-positive lesions in other non-irradiated sites are eligible to be included in the group;
Received donor lymphocyte infusion (DLI) within 6 weeks before CAR-T cell infusion;
If anti-PD1, PD-L1 and other immunotherapies have been used before CAR-T cell reinfusion, at least 5 half-lives must elapse between the last medication and before CAR-T cell reinfusion;
History or presence of CNS disorder, such as seizure disorder, cerebrovascular ischemia/hemorrhage, dementia, cerebellar disease, cerebral edema, posteriorreversible encephalopathy syndrome, or any autoimmune disease with CNS involvement;
Received autologous transplantation within 6 weeks before the start of screening;
Subjects has HBV, HCV, HIV ,EBV,ECV or syphilis infection at the time of screening;
Live vaccine received within 6 weeks before the start of screening;
History of myocardial infarction, cardiac angioplasty or stenting, unstable angina,active arrhythmias, or other clinically significant cardiac disease within 6 months of enrollment;
History of symptomatic deep vein thrombosis or pulmonary embolism within 6 months of enrollment;
History of malignancy other than nonmelanomatous skin cancer or carcinoma in situ (eg, cervix, bladder, breast) unless disease-free for at least 3 years；
Presence of fungal, bacterial, viral, or other infection that is uncontrolled or requiring intravenous (IV) antimicrobials for management. Simple urinary tract infection (UTI) and bacterial pharyngitis are permitted if the investigator evaluates that it can be controlled by treatment, they can be included in the group;
In the investigator's judgment, the subject is unlikely to complete all protocol-required study visits or procedures, including follow-up visits, or comply with the study requirements for participation.