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Study Ref. Design studied treatmentcontrol treatmentpatientsstudy risk of biassample sizes Results

COVID 19 hospitalized meta-analysis

Declercq J (COV-AID)
 
NCT04330638
RCTtocilizumab standard of careCOVID 19 hospitalizedlow
114/115 inconclusive
    RCT-TCZ-COVID-19
     
    NCT04346355
    RCTtocilizumab standard of careCOVID 19 hospitalizedsome concern
    60/66 inconclusive
      RECOVERY
       
      NCT04381936
      RCTtocilizumab standard of careCOVID 19 hospitalizedsome concern
      2022/2094 conclusif
      • demonstrated 15 % decrease in deaths (PE) with a moderate degree of certainty due to some concern in risk of bias
      • suggested 15 % decrease in death or ventilation with a moderate degree of certainty due to some concern in risk of bias
      Rutgers RCTtocilizumab standard of careCOVID 19 hospitalizedsome concern
      174/180 suggested
      • inconclusive 41 % decrease in death D28 (PE) with a moderate degree of certainty due to some concern in risk of bias
      • suggested 35 % decrease in death or ventilation with a moderate degree of certainty due to some concern in risk of bias
      Soin AS (COVINTOC)
       
      CTRI/2020/05/025369
      RCTtocilizumab standard of careCOVID 19 hospitalizedsome concern
      90/90 inconclusive
        Dongsheng Wang
         
        ChiCTR2000029765
        RCTtocilizumab standard of careCOVID 19 hospitalizedsome concern
        33/32 safety concern
        • statistically significant 8.6-fold increase in adverse events with a moderate degree of certainty due to some concern in risk of bias
        EMPACTA
         
        NCT04372186
        RCTtocilizumab placeboCOVID 19 hospitalizedsome concern
        259/129 conclusif
        • demonstrated 44 % decrease in death or ventilation (PE) with a moderate degree of certainty due to some concern in risk of bias
        • suggested 45 % decrease in clinical deterioration with a moderate degree of certainty due to some concern in risk of bias
        EU-CTR2020-001375-32 (PreToVid) unpublished
         
        EU-CTR2020-001375-32
        RCTtocilizumab standard of careCOVID 19 hospitalizedlow
        174/180 inconclusive
          EU-CTR2020-001748-24 (ImmCoVA) unpublished
           
          EU-CTR2020-001748-24
          RCTtocilizumab standard of careCOVID 19 hospitalizedlow
          22/27 inconclusive
            NCT04412772 (ARCHITECTS) unpublished
             
            NCT04412772
            RCTtocilizumab placeboCOVID 19 hospitalizedlow
            10/11 inconclusive
              NCT04434717 (COVITOZ-1 single dose plus two doses) unpublished
               
              NCT04434717
              RCTtocilizumab standard of careCOVID 19 hospitalizedlow
              17/9 inconclusive
                NCT04479358 (COVIDOSE-2 substudy A 120mg plus 40mg) unpublished
                 
                NCT04479358
                RCTtocilizumab standard of careCOVID 19 hospitalizedlow
                20/8 inconclusive
                  NCT04577534 (COVIDSTORM) unpublished
                   
                  NCT04577534
                  RCTtocilizumab standard of careCOVID 19 hospitalizedlow
                  26/13 inconclusive
                    Colaneri OBStocilizumab controlCOVID 19 hospitalizedcritical
                    21/21 inconclusive
                      HNF Hospital Tocilizumab multidisciplinary team OBStocilizumab controlCOVID 19 hospitalizedcritical
                      20/25 suggested
                      • suggested 87 % decrease in death or transfer to ICU but with a very low degree of certainty due to critical risk of bias
                      Martinez-Sanz OBStocilizumab controlCOVID 19 hospitalizedcritical
                      260/969 suggested
                      • suggested 66 % decrease in deaths but with a very low degree of certainty due to critical risk of bias
                      Tsai OBStocilizumab controlCOVID 19 hospitalizedserious
                      66/66 inconclusive

                        COVID 19 all comers meta-analysis

                        BACC Bay Tocilizumab Trial
                         
                        NCT04356937
                        RCTtocilizumab placeboCOVID 19 all comerslow
                        161/81 inconclusive
                        • inconclusive 17 % decrease in death or ventilation (PE) with a high degree of certainty due to low risk of bias
                        TOCOVID unpublished
                         
                        NCT04332094
                        RCTtocilizumab standard of careCOVID 19 all comersNA
                        136/134 inconclusive

                          COVID-19 mild to moderate meta-analysis

                          Capra OBStocilizumab controlCOVID-19 mild to moderatecritical
                          62/23 suggested
                          • suggested 96 % decrease in deaths,deaths (time to event analysis only) but with a very low degree of certainty due to critical risk of bias

                          COVID-19 severe or critically meta-analysis

                          Hamed RCTtocilizumab standard of careCOVID-19 severe or criticallyhigh
                          26/23 inconclusive
                          • inconclusive 83 % increase in deaths (PE) but with a low degree of certainty due to high risk of bias
                          • inconclusive 2.2-fold increase in ICU admission (PE) but with a low degree of certainty due to high risk of bias
                          REMAP-CAP (tocilizumab)
                           
                          NCT02735707
                          RCTtocilizumab standard of careCOVID-19 severe or criticallysome concern
                          353/402 conclusif
                          • suggested 30 % decrease in deaths with a moderate degree of certainty due to some concern in risk of bias
                          • demonstrated 64 % increase in clinical improvement (PE) with a moderate degree of certainty due to some concern in risk of bias
                          Rosas (REMDACTA)
                           
                          NCT04409262
                          RCTtocilizumab placeboCOVID-19 severe or criticallysome concern
                          434/215 inconclusive
                          • inconclusive 3 % decrease in hospital discharge (PE) with a moderate degree of certainty due to some concern in risk of bias
                          Talaschian
                           
                          IRCT20081027001411N4
                          RCTtocilizumab standard of careCOVID-19 severe or criticallysome concern
                          20/20 inconclusive
                            Veiga
                             
                            NCT04403685
                            RCTtocilizumab standard of careCOVID-19 severe or criticallysome concern
                            65/64 safety concern
                            • safety concern with 1.7-fold increase in deaths,death D28 (not statistically significant)
                            • inconclusive 54 % increase in death or ventilation (PE) with a moderate degree of certainty due to some concern in risk of bias
                            CORIMUNO-TOCI-1 (Group 1)
                             
                            NCT04331808
                            RCTtocilizumab standard of careCOVID-19 severe or criticallysome concern
                            64/67 inconclusive
                              CORIMUNO-TOCI-ICU (Group 2)
                               
                              NCT04331808
                              RCTtocilizumab standard of careCOVID-19 severe or criticallysome concern
                              49/43 inconclusive
                                COVACTA (Rosas)
                                 
                                NCT04320615
                                RCTtocilizumab placeboCOVID-19 severe or criticallysome concern
                                301/151 suggested
                                • inconclusive 19 % increase in clinical improvement,clinical improvement (28-day) (PE) with a moderate degree of certainty due to some concern in risk of bias
                                NCT04377750 (HMO-0224-20) unpublished
                                 
                                NCT04377750
                                RCTtocilizumab placeboCOVID-19 severe or criticallyhigh
                                37/17 inconclusive
                                  Andrew OBStocilizumab controlCOVID-19 severe or criticallyNA
                                  198/413 inconclusive
                                    Biran OBStocilizumab controlCOVID-19 severe or criticallyserious
                                    210/420 suggested
                                    • suggested 36 % decrease in deaths but with a low degree of certainty due to high risk of bias
                                    Mathilde OBStocilizumab controlCOVID-19 severe or criticallycritical
                                    30/29 suggested
                                    • suggested 75 % decrease in deaths but with a very low degree of certainty due to critical risk of bias
                                    Rojas-Marte OBStocilizumab controlCOVID-19 severe or criticallycritical
                                    96/97 inconclusive
                                      Somers OBStocilizumab controlCOVID-19 severe or criticallycritical
                                      78/76 safety concern
                                      • suggested 45 % decrease in deaths,deaths (time to event analysis only) but with a very low degree of certainty due to critical risk of bias
                                      • statistically significant 2.3-fold increase in superinfection but with a very low degree of certainty due to critical risk of bias
                                      TOCI-RAF Study Group (Campochiaro) OBStocilizumab controlCOVID-19 severe or criticallyNA
                                      32/33 inconclusive

                                        PE: primary endpoint; (a): to be demonstrated a result must be statistically significant on a primary endpoint (with multiplicity adjustment if necessary);
                                        Study risk of bias assessed for the study primary endpoint(s) or the main endpoints in case of no formally defined primary endpoint(s).