A phase I, ascending dose, to evaluate safety and efficacy of ADP A2M4CD8 in HLA-A2+ patients with MAGE-A4 psoitives tumors

Long title

A phase I, ascending dose, to evaluate safety and efficacy of ADP A2M4CD8 in HLA-A2+ patients with MAGE-A4 psoitives tumors

Date receipt dossier

EU record number

ADP-0055-001

EudraCT number

2019-001965-34

Company / Sponsor

Adaptimmune LLC

Phase

I

Treated organism

Humans

Indication category

Cancer therapy

Disease

MAGE-A4 positive tumors

Therapeutic approach

Immunotherapy

Genetic modification

MAGE-A4 specific T cell receptor (TCR) with a CD8α co-receptor

Method of transfer of nucleic acid of interest

Lentiviral vectors

Administered biological material

Autologous T cells transduced with lentiviral vectors expressing a MAGE-A4 specific T cell receptor (TCR) with a CD8α co-receptor.

Route of administration

Intravenous

Locations in Belgium

Cliniques Universitaires Saint-Luc; UZ Antwerpen; U Gent

Type of procedure

Contained use only

Current status

Authorized

Pharmaceutical study code

A2M4CD8

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