| 
            B/BE/24/BVW4           | 
                  
            A phase 3 multinational, open-label, systemic gene delivery study to evaluate the safety and efficacy of SRP-9003 in subjects with limb girdle muscular dystrophy 2E/R4           | 
                  
                  
            Humans           | 
                  
            Non-replicating recombinant vector derived from adeno-associated virus AAV, serotype rh74, lacking all AAV viral genes and carrying the full-length sarcoglycan-beta (SGCB) gene           | 
              
          
                  | 
            B/BE/22/BVW6           | 
                  
            A phase 3, Multinational, Randomized, Double-Blind, Placebo-Controlled Systemic Gene Transfer Therapy Study to Evaluate the Safety and Efficacy of SRP-9001 in Non-Ambulatory and Ambulatory Subjects With Duchenne Muscular Dystrophy (ENVISION)           | 
                  
                  
            Humans           | 
                  
            Non-replicating recombinant vector derived from adeno-associated virus AAV, serotype rh74, lacking all AAV viral genes and carrying the human micro-dystrophin (hMicro-Dys) gene           | 
              
          
                  | 
            B/BE/21/BVW5           | 
                  
            A Phase 3 Multinational, Randomized, Double-Blind, Placebo-Controlled Systemic Gene Delivery Study to Evaluate the Safety and Efficacy of SRP-9001 in Subjects With Duchenne Muscular Dystrophy (EMBARK)           | 
                  
                  
            Humans           | 
                  
            Non-replicating recombinant vector derived from adeno-associated virus AAV, serotype rh74, lacking all AAV viral genes and carrying the human micro-dystrophin (hMicro-Dys) gene           | 
              
          
                  | 
            MB-CART2019.1           | 
                  
            A phase I/II safety, dose finding and feasibility trial of MB-CART2019.1 in patients with relapsed or resistant B-NHL           | 
                  
                  
            Humans           | 
                  
            CD19 and CD20 chimeric antigen receptor           | 
              
          
                  | 
            B/BE/98/B6           | 
                  
            Clinical research program : Gene-therapy by the Use of a Recombinant Adenovirus in the Treatment of p53 Deficient Cancers           | 
                  
                  
            Humans           | 
                  
            wild-type p53 tumor suppressor gene           | 
              
          
                  | 
            Only notified under the "contained use" procedure. Dossier submitted on 18/08/1997.           | 
                  
            A phase II gene therapy study in patients with non-small cell lung cancer using SCH58500 (rAd/p53) in combination with chemotherapy for multiple cycles            | 
                  
                  
            Humans           | 
                  
            Wild-type p53           | 
              
          
                  | 
            Only notified under the "contained use" procedure. Dossier submitted on 21/10/1996.           | 
                  
            A phase I study in patients with recurrent or metastatic squamous cell carcinoma of the head and neck using SCH 58500 (rAd/p53) administered by single intratumoral injection           | 
                  
                  
            Humans           | 
                  
            Wild-type p53            |