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            B/BE/25/BVW2           | 
                  
            A randomised, double-blind, placebo-controlled, single centre, Phase I study to evaluate the safety, reactogenicity and immunogenicity of AstriVax’ investigational therapeutic hepatitis B virus (HBV) vaccine (AVX70371) in healthy adults aged 18 to 40 year           | 
                  
                  
            Humans           | 
                  
            Full genome of the live attenuated yellow fever virus (YFV) strain 17D (YF17D) containing the sequence of the HBV core antigen (HBc)            | 
              
          
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            B/BE/24/BVW6           | 
                  
            A randomised, double-blind, placebo-controlled, multi-centre, Phase I study to evaluate the safety, reactogenicity and immunogenicity of AstriVax’ investigational therapeutic hepatitis B virus (HBV) vaccine (AVX70371) in adult patients with chronic HBV           | 
                  
                  
            Humans           | 
                  
            Full genome of the live attenuated yellow fever virus (YFV) strain 17D (YF17D) containing the sequence of the HBV core antigen (HBc)            | 
              
          
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            B/BE/23/BVW3           | 
                  
            A Phase I, randomized, double-blind, multi-centre, placebo-controlled, dose-escalation study to evaluate the safety, reactogenicity and immunogenicity of AstriVax’ investigational vaccine for the prevention of yellow fever (AVX70120), and of AstriVax’ inv           | 
                  
                  
            Humans           | 
                  
            Full genome of the live attenuated yellow fever virus (YFV) strain 17D (YF17D) containing the sequence of the surface glycoprotein from the rabies virus (RabG)            | 
              
          
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            Only notified under the "contained use" procedure. Dossier submitted on 22/05/2023.           | 
                  
            A randomized, open-label, Phase 2 study evaluating lymphodepletion with fludarabine (F), cyclophosphamide (C), and ALLO-647 (A) vs FC alone, in subjects with R/R LBCL receiving ALLO-501A allogeneic CAR T cell therapy           | 
                  
                  
            Humans           | 
                  
            CD19 CAR + knockouts CD52 and TRAC via TALEN technology           | 
              
          
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            Only notified under the "contained use" procedure. Dossier submitted on 04/10/2018.           | 
                  
            A Phase 3, Randomized, Double-blind, Placebo-controlled study to Determine the Efficacy and Safety of CMB305 in Unresectable Locally-advanced or Metastatic NY-ESO-1 + Synovial Sarcoma Subjects Following First-line Systemic Anti-cancer Therapy           | 
                  
                  
            Humans           | 
                  
            Replication deficient lentiviral vector encoding NY-ESO-1 cancer testis antigen           |