| 
            Only notified under the "contained use" procedure. Dossier submitted on 02/12/2019.           | 
                  
            A multicentre, open-label, single ascending dose, dose-ranging, phase I/Iia study to evaluate the safety and tolerability of an autologous antigen-specific chimeric antigen receptor T regulatory cell therapy (TX200-TR101) in living donor renal transplant            | 
                  
                  
            Humans           | 
                  
            chimeric antigen receptor specific to the donor HLA A*2           | 
              
          
                  | 
            ADP-0055-001           | 
                  
            A phase I, ascending dose, to evaluate safety and efficacy of ADP A2M4CD8 in HLA-A2+ patients with MAGE-A4 psoitives tumors           | 
                  
                  
            Humans           | 
                  
            MAGE-A4 specific T cell receptor (TCR) with a CD8α co-receptor             | 
              
          
                  | 
            Only notified under the "contained use" procedure. Dossier submitted on 24/04/2017.           | 
                  
            A Phase 1, Open Label, Non-comparative Study to Evaluate the Safety and the Ability of UCART19 to Induce Molecular Remission in Paediatric Patients With Relapsed/Refractory B Acute Lymphoblastic Leukaemia           | 
                  
                  
            Humans           | 
                  
            chimeric antigen receptor and suicide-ligand (RQR8)           |