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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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            COVID-19-101           | 
                  
            A randomized, placebo-controlled trial, to evaluate the safety and immunogenicity of the COVID-19 vaccine, a measles vector-based vaccine candidate against COVID-19 in healthy volunteers consisting of an unblinded dose escalation and a blinded treatment p           | 
                  
                  
            Humans           | 
                  
            Recombinant measles virus vaccine strain (Schwarz strain) expressing the Spike glycoprotein 1 from SARS-CoV2           | 
              
          
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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           | 
              
          
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            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             | 
              
          
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            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           | 
              
          
                  | 
            Only notified under the "contained use" procedure. Dossier submitted on 13/10/2000.           | 
                  
            A phase III open-label, comparative, multicentre trials to test the concept of durable virologic suppression in subjects with primary HIV-1 infection after intensive induction of quadruple HAART followed by double-blind randomization to HIV vaccination wi           | 
                  
                  
            Humans           | 
                  
            vCP-1452           |