| 
            Only notified under the "contained use" procedure. Dossier submitted on 18/11/2021.           | 
                  
            A Randomized, Double-blind, Placebo-controlled Phase III Study to Evaluate the Safety and Immunogenicity of an Ad26,RSV,preF-based Vaccine in Adults Aged 18 to 59 years, Including Those at High-risk for severe RSV           | 
                  
                  
            Humans           | 
                  
            Replication deficient Adenovirus serotype 26 containing a deoxyribonucleic acid (DNA) transgene that encodes the pre-fusion conformation-stabilized F protein (pre-F) derived from the RSV A2 strain           | 
              
          
                  | 
            J&JBE-018_004           | 
                  
            A randomized, double-blind, placebo-controlled Phase 1/2a study to evaluate the safety, reactogenicity, and immunogenicity of Ad26COVS1 in adults aged 18 to 65 years, inclusive and adults aged 65 years and older.           | 
                  
                  
            Humans           | 
                  
            Recombinant Adenoviral vector serotype 26 expressing the spike glycoprotein 1 from SARS-CoV2            | 
              
          
                  | 
            Only notified under the "contained use" procedure. Dossier submitted on 05/10/2018.           | 
                  
            Open-label, Single-arm Phase 1 Study to Evaluate the Shedding, Biodistribution, Safety and Immunogenicity of Ad26.RSV.preF Vaccine in Adults           | 
                  
                  
            Humans           | 
                  
            Replication deficient Adenovirus serotype 26 containing a deoxyribonucleic acid (DNA) transgene that encodes the pre-fusion conformation-stabilized F protein (pre-F) derived from the RSV A2 strain           | 
              
          
                  | 
            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           | 
              
          
                  | 
            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            |