| 
            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)           | 
              
          
                  | 
            B/BE/03/B3           | 
                  
            Phase I multicentre study of TG1024 (Adenovirus interleukin 2) in patients with metastatic melanoma or other advanced solid tumor cancers           | 
                  
                  
            Humans           | 
                  
            gene coding for human interleukin 2           | 
              
          
                  | 
            B/BE/02/B7           | 
                  
            Phase II study evaluating the clinical efficacy of TG4010 (MVA-MUC1-IL2) in patients with metastatic Renal Cell Carcinoma (RCC)            | 
                  
                  
            Humans           | 
                  
            sequences coding for the human MUC-1 antigen and IL-2           | 
              
          
                  | 
            B/BE/01/B7           | 
                  
            Specific immunotherapy against MUC-1 antigen - Study TG4010.04 : "Phase II study with TG4010(MVA-MUC-1-IL-2) in patients with metastatic breast cancer", Study TG4010.05 : "Phase II study with TG 4010 in patients with non small cell lung cancer"             | 
                  
                  
            Humans           | 
                  
            sequences coding for the human MUC-1 antigen and IL-2           | 
              
          
                  | 
            Only notified under the "contained use" procedure. Dossier submitted on 09/11/2001.           | 
                  
            A phase III, multi-center, open-label, randomized study to compare the overall survival and safety of bi-weekly intratumoral administration of INGN 201 versus weekly methotrewate in 240 patients with refractory squamous cell carcinoma of the head and neck           | 
                  
                  
            Humans           | 
                  
            Wild-type p53            | 
              
          
                  | 
            Only notified under the "contained use" procedure. Dossier submitted on 09/11/2001.           | 
                  
            A phase III, multi-center, open-label, randomized study to compare the effectiveness and safety of intratumoral administration of INGN 201 in combination with chemotherapy versus chemotherapy alone in 288 patients with recurrent squamous cell carcinoma of           | 
                  
                  
            Humans           | 
                  
            Wild-type p53            |