| 
            Only notified under the "contained use" procedure. Dossier submitted on 18/01/2024.           | 
                  
            A phase I/II, multicenter study evaluating the feasibility, safety, and efficacy of point-of-care manufactured GLPG5101 (19CP02) in subjects with relapsed/refractory B-cell non-Hodgkin lymphoma (r/r NHL) (CP0201-NHL)           | 
                  
                  
            Humans           | 
                  
            BCMA CAR           | 
              
          
                  | 
            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 13/10/2000.           | 
                  
            A phase III open-label, comparative, multicentre trials to test the concept of durable virologic suppression in subjects with primary HIV-1 infection after intensive induction of quadruple HAART followed by double-blind randomization to HIV vaccination wi           | 
                  
                  
            Humans           | 
                  
            vCP-1452           |