A phase II, multicenter study to determine the efficacy and safety of bb2121 in subjects with relapsed and refractory multiple myeloma

Long title

A phase II, multicenter study to determine the efficacy and safety of bb2121 in subjects with relapsed and refractory multiple myeloma

Date receipt dossier

EU record number

bb2121-MM-001

EudraCT number

2017-002245-29

Company / Sponsor

Celgene

Phase

II

Treated organism

Humans

Indication category

Cancer therapy

Disease

relapsed and refractory multiple myeloma

Therapeutic approach

Immunotherapy

Genetic modification

BCMA02 (human B cell maturation antigen)-CAR

Method of transfer of nucleic acid of interest

Lentiviral vectors

Administered biological material

Autologous T-cells transduced with lentiviral vectors expressing BCMA02 (human B cell maturation antigen) CAR

Route of administration

Intravenous

Locations in Belgium

UZ Leuven

Type of procedure

Contained use only

Current status

Authorized

Pharmaceutical study code

bb2121

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