| 
            B/BE/24/BVW5           | 
                  
            Phase 3, open-label, single-arm study to evaluate efficacy and safety of FIX gene transfer with PF-06838435 (rAAV-Spark100-hFIX-R338L) in adult male participants with moderately severe to severe hemophilia B (FIX:C ≤2%) (BeneGene-2)           | 
                  
                  
            Humans           | 
                  
            Recombinant adeno associated viral vector containing the  codon-optimised human factor IX (FIX) minigene (R338L variant)            | 
              
          
                  | 
            B/BE/20/BVW6           | 
                  
            Dossier withdrawn by the notifier           | 
                  
                  
            Humans           | 
                  
            Non-replicating recombinant vector derived from adeno-associated virus AAV6 serotype, containing a codon-optimised version of the human Factor VIII gene           | 
              
          
                  | 
            B/BE/20/BVW4           | 
                  
            A Phase 3, Multicenter, Randomized, Double-Blind, Placebo-Controlled Study to Evaluate the Safety and Efficacy of PF-06939926 for the Treatment of Duchenne Muscular Dystrophy           | 
                  
                  
            Humans           | 
                  
            Non-replicating recombinant vector derived from adeno-associated virus AAV9, lacking all AAV viral genes and containing a miniaturized version of the human dystrophin gene           | 
              
          
                  | 
            B/BE/11/V3           | 
                  
            Evaluation of the safety and efficacy of the vaccine PB-116 in the control of porcine pleuropneumonia caused by Actinobacillus pleuropneumoniae           | 
                  
                  
            pigs           | 
                  
            no new genes but deletion of a segment of gene A from which depends the haemolytic activity of the pathogen           | 
              
          
                  | 
            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            |