Study of T Cells Targeting CD138/BCMA/CD19/More Antigens (CART-138/BCMA/19/More) for Chemotherapy Refractory and Relapsed Multiple Myeloma

Who is this study for? Patients with Multiple Myeloma
What treatments are being studied? CART-138/BCMA/19/More
Status: Recruiting
Location: See location...
Intervention Type: Biological
Study Type: Interventional
Study Phase: Phase 1/Phase 2
SUMMARY

Placing a tumor antigen chimeric receptor that has been created in the laboratory into patient autologous or donor-derived T cells may make the body build immune response to kill cancer cells. Genetically engineered lymphocyte (CART) therapy has showed good safety and efficacy in treatment of lymphoma and acute lymphoblastic leukemia. Researchers want to see if this helps people with multiple myeloma.To test the safety and efficacy of giving targeting CD138 or B-cell maturation antigen or CD19 or more antigens T cells in treating patients with multiple myeloma that is refractory to further chemotherapy or relapsed(after stem cell transplantation or intensive chemotherapy).

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Maximum Age: 75
Healthy Volunteers: t
View:

• CD138 or BCMA antigen positive multiple myeloma in patients with no available curative treatment options (such as autologous or allogeneic SCT).

• Relapsed and/or refractory multiple myeloma.

• Relapsed after prior autologous or allogenic SCT.

• Expected survival ≥ 3 months

• Creatinine \< 2.0 mg/dl

• Blood coagulation function: PT and APTT \< 2x normal

• Arterial blood oxygen saturation \> 92%

• Alanine Aminotransferase (ALT)/Aspartate Aminotransferase (AST) \< 3x normal

• Karnofsky scores ≥ 60 and ECOG score ≤ 2

• Adequate venous access for apheresis, and no other contraindications for leukapheresis

• Patients should not take system chemotherapy in one month and immunotherapy in three months prior to CART cells infusion.

• Voluntary informed consent is given

Locations
Other Locations
China
First Affiliated Hospital, Soochow University
RECRUITING
Suzhou
Contact Information
Primary
Ling zhi Yan, PhD
yanlingzhi@suda.edu.cn
13584821140
Time Frame
Start Date: 2016-09
Estimated Completion Date: 2026-12
Participants
Target number of participants: 10
Treatments
Experimental: CART-138/BCMA/19/more
Sponsors
Leads: The First Affiliated Hospital of Soochow University

This content was sourced from clinicaltrials.gov