Safety of MB-CART2019.1 in Lymphoma Patients (MB-CART2019.1 Lymphoma / DALY 1)

PHASE1CompletedINTERVENTIONAL
Enrollment

12

Participants

Timeline

Start Date

February 25, 2019

Primary Completion Date

December 17, 2020

Study Completion Date

May 28, 2024

Conditions
B-cell Non Hodgkin Lymphoma
Interventions
BIOLOGICAL

MB-CART2019.1 Dose level 1

This is a prospective, multi-center, open phase I/II trial to evaluate feasibility, dosage, safety and toxicity as well as efficacy of ex vivo expanded autologous T cells genetically modified to express anti-CD20 and CD19 immunoreceptor (MBCART2019.1) in patients with relapsed or resistant aggressive CD20 and CD19 positive B-NHL/CLL/SLL.

BIOLOGICAL

MB-CART2019.1 Dose level 2

This is a prospective, multi-center, open phase I/II trial to evaluate feasibility, dosage, safety and toxicity as well as efficacy of ex vivo expanded autologous T cells genetically modified to express anti-CD20 and CD19 immunoreceptor (MBCART2019.1) in patients with relapsed or resistant aggressive CD20 and CD19 positive B-NHL.

Trial Locations (3)

20246

Universitätsklinikum Hamburg-Eppendorf, Department of Stem Cell Transplantation, Hamburg

50937

University Hospital Cologne - Department for Internal Medicine I, Cologne

86156

Klinikum Augsburg, II. Med. Klinik Haematologie / Onkologie, Augsburg

Sponsors

Collaborators (1)

All Listed Sponsors
collaborator

ICON plc

INDUSTRY

lead

Miltenyi Biomedicine GmbH

INDUSTRY