A Phase I/II, multicenter study, evaluating the feasibility, safety, and efficacy of point-of-care manufactured 19CP02 in subjects with relapsed/refractory B-cell non-Hodglin lymphoma

Long title

A Phase I/II, multicenter study, evaluating the feasibility, safety, and efficacy of point-of-care manufactured 19CP02 in subjects with relapsed/refractory B-cell non-Hodglin lymphoma

Date receipt dossier

EU record number

CP0201-NHL

EudraCT number

2021-003272-13

Company / Sponsor

CellPoint B.V.

Phase

I/II

Treated organism

Humans

Indication category

Cancer therapy

Disease

Lymphomas non-Hodgkin's B-cell

Therapeutic approach

Immunotherapy

Genetic modification

CD19-CAR

Method of transfer of nucleic acid of interest

Lentiviral vector

Administered biological material

Autologous T-cells transduced with lentiviral vectors against CD19-CAR

Route of administration

Intravenous

Locations in Belgium

CHU de Liège, UZA

Type of procedure

Contained use only

Current status

Authorized

Pharmaceutical study code

19CP02

© Sciensano - Version 1.0 (20260902.1)