Study explorer (study characteristics and results) method abbreviations pdf   xlsx

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

COVID 19 hospitalized meta-analysis

CORIMUNO-SARI-1 (non ICU)
 
NCT04324073
RCTsarilumabstandard of careCOVID 19 hospitalizedsome concern
68/80 inconclusive
  • inconclusive 1 % increase in clinical deterioration (PE) with a moderate degree of certainty due to some concern in risk of bias
  • inconclusive 12 % increase in death or ventilation (PE) with a moderate degree of certainty due to some concern in risk of bias
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
                          MARIPOSA
                           
                          NCT04363736
                          RCTtocilizumab tocilizumab COVID-19 severe or criticallysome concern
                          48/49 inconclusive
                            A trend for increased progression toward worse clinical status (categories 5 and 6) and death (category 7) was seen up to day 14 for the 4-mg/kg vs 8-mg/ kg group, followed by no notable difference between groups at days 21 and 28.
                            Rashad
                             
                            NCT04519385
                            RCTtocilizumab dexamethasoneCOVID-19 severe or criticallyhigh
                            74/75 safety concern
                            • statistically significant 1.2-fold increase in deaths,deaths (time to event analysis only) (PE) but with a low degree of certainty due to high risk of bias
                            • statistically significant 1.9-fold increase in death D28 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
                            REMAP-CAP sarilumab
                             
                            NCT02735707
                            RCTsarilumabstandard of careCOVID-19 severe or criticallyhigh
                            48/402 conclusif
                            • demonstrated 76 % increase in clinical improvement (PE) but with a low degree of certainty due to high risk of bias
                            • suggested 86 % increase in clinical improvement (14-day) but with a low degree of certainty due to high 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
                                      ARI-RAF (Della-Torre) OBSsarilumabcontrolCOVID-19 severe or criticallyNA
                                      28/28 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).