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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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            CYAD-211-001           | 
                  
            An open-label phase I, multi-center study to determine the recommended dose of the chimeric antigen receptor T-cell treatment CYAD-211 after a non-myeloablative preconditioning chemotherapy in multiple myeloma patients with relapsed or refractory disease.           | 
                  
                  
            Humans           | 
                  
            BCMA-CAR and ShRNA CD3ζ           | 
              
          
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            CYAD-N2T-005           | 
                  
            An open-label, Phase I/II study to assess the safety and clinical activity of NKR-2 treatment administration after non-myeloablative preconditioning chemotherapy in relapse/refractory acute myeloid leukemia or myelodysplasic syndrome patient (DEPLETHINK -           | 
                  
                  
            Humans           | 
                  
            NKG2D-chimeric antigen receptor           | 
              
          
                  | 
            CYAD-02-001           | 
                  
            An open-label, phase I, multi-center study to determine in relapsed/refractory acute myeloid leukemia or myelodysplasic syndrome patients the recommended dose of CYAD-02 after a non-myeloablative preconditioning chemotherapy followed by a potential CYAD-0           | 
                  
                  
            Humans           | 
                  
            NKG2D-chimeric antigen receptor, ShRNA targeting the endogenous RNA of NKG2D ligands MICA and MICB and truncated CD19 reporter protein           | 
              
          
                  | 
            CYAD-N2L-101           | 
                  
            An open-label, Phase I study to assess the safety of multiple doses of CYAD-101, administered after standard FOLFOX chemotherapy in patients with unresectable metastatic colorectal cancer (alloSHRINK-study-Standard cHemotherapy Regimen and Immunotherapy w           | 
                  
                  
            Humans           | 
                  
            NKG2D-chimeric antigen receptor, the truncated CD19 tag and the TIM8 molecule which interferes with the interaction between the natural TCR and endogenous CD3ζ             | 
              
          
                  | 
            CYAD-N2T-006            | 
                  
            An open-label, phase I study to assess the safety of NKR-2 treatment administrated concurrently with 5-azacytidine in tretment-naïve acute myeloid leukemia or myelodysplastic syndrome patients not candidates for intensive therapy (EPITHINK - EPIgenetic dr           | 
                  
                  
            Humans           | 
                  
            NKG2D-chimeric antigen receptor           | 
              
          
                  | 
            Only notified under the "contained use" procedure. Dossier submitted on 25/10/2016.           | 
                  
            A multinational, open-label, dose escalation Phase I/II study to assess the safety and clinical activity of multiple administrations of NKR-2 in patients with different metastatic tumor types           | 
                  
                  
            Humans           | 
                  
            NKG2D-chimeric antigen receptor           | 
              
          
                  | 
            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           |