A phase I/II open label, multicenter study evaluating the feasibility, safety and efficacy of point-of-care manufactured anti-BCMA CAR T cells (BCMACP03) in subjects with relapsed/refractory Multiple Myeloma (r/r MM) (Papilio-1)

Long title

A phase I/II open label, multicenter study evaluating the feasibility, safety and efficacy of point-of-care manufactured anti-BCMA CAR T cells (BCMACP03) in subjects with relapsed/refractory Multiple Myeloma (r/r MM) (Papilio-1)

Date receipt dossier

EudraCT number

2022-500782-27

Company / Sponsor

CellPoint B.V. (a Galapagos company)

Phase

I/II

Treated organism

Humans

Indication category

Cancer therapy

Disease

Multiple Myeloma

Therapeutic approach

Immunotherapy

Genetic modification

BCMA CAR

Method of transfer of nucleic acid of interest

Lentiviral vector

Administered biological material

Autologous T cells transduced with lentiviral vectors expressing BCMA-CAR

Route of administration

Intravenous

Locations in Belgium

CHU de Liège, UZA, UZ Leuven, AZ Delta

Type of procedure

Contained use only

Current status

Authorized

Pharmaceutical study code

BCMACP03, GLPG5301

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