Ongoing Clinical Trials: therapeutics against cytokine storm (up to May 6, 2020)
Register Number . | Title . | Drugs/Strategies . | Therapeutic Target . | Study design . | Samples . | Phase . |
---|---|---|---|---|---|---|
ChiCTR2000029765 | A multicenter, randomized controlled trial for the efficacy and safety of tocilizumab in the treatment of new coronavirus pneumonia (COVID-19) | Tocilizumab | Anti-IL-6 Receptor | RCT | 188 | 4 |
ChiCTR2000030196 | A multicenter, single arm, open label trial for the efficacy and safety of CMAB806 in the treatment of cytokine release syndrome of novel coronavirus pneumonia (COVID-19) | Tocilizumab | Anti-IL-6 Receptor | Single arm | 60 | 2 |
NCT04317092 | Tocilizumab in COVID-19 Pneumonia (TOCIVID-19) | Tocilizumab | Anti-IL-6 Receptor | Single arm | 330 | 2 |
NCT04320615 | A Study to Evaluate the Safety and Efficacy of Tocilizumab in Patients with Severe COVID-19 Pneumonia | Tocilizumab | Anti-IL-6 Receptor | RCT | 330 | 3 |
NCT04310228 | Favipiravir Combined with Tocilizumab in the Treatment of Corona Virus Disease 2019 | Tocilizumab | Anti-IL-6 Receptor | RCT | 150 | N/A |
NCT04306705 | Tocilizumab vs CRRT in Management of Cytokine Release Syndrome (CRS) in COVID-19 | Tocilizumab | Anti-IL-6 Receptor | Cohort study | 120 | N/A |
NCT04315480 | Tocilizumab for SARS-CoV2 Severe Pneumonitis | Tocilizumab | Anti-IL-6 Receptor | Single arm | 30 | 2 |
NCT04331795 | Tocilizumab to Prevent Clinical Decompensation in Hospitalized, Non-critically Ill Patients With COVID-19 Pneumonitis | Tocilizumab | Anti-IL-6 Receptor | RCT | 50 | 2 |
NCT04331808 | CORIMUNO-19 - Tocilizumab Trial - TOCI (CORIMUNO-TOCI) | Tocilizumab | Anti-IL-6 Receptor | RCT | 240 | 2 |
NCT04332913 | Efficacy and Safety of Tocilizumab in the Treatment of SARS-Cov-2 Related Pneumonia | Tocilizumab | Anti-IL-6 Receptor | Cohort study | 30 | N/A |
NCT04335071 | Tocilizumab in the Treatment of Coronavirus Induced Disease (COVID-19) | Tocilizumab | Anti-IL-6 Receptor | RCT | 100 | 2 |
NCT04346355 | Efficacy of Early Administration of Tocilizumab in COVID-19 Patients | Tocilizumab | Anti-IL-6 Receptor | RCT | 398 | 2 |
NCT04356937 | Efficacy of Tocilizumab on Patients With COVID-19 | Tocilizumab | Anti-IL-6 Receptor | RCT | 300 | 3 |
NCT04359667 | Serum IL-6 and Soluble IL-6 Receptor in Severe COVID-19 Pneumonia Treated With Tocilizumab | Tocilizumab | Anti-IL-6 Receptor | Case | 30 | N/A |
NCT04361032 | Assessment of Efficacy and Safety of Tocilizumab Compared to Deferoxamine, Associated With Standards Treatments in COVID-19 (+) Patients Hospitalized In Intensive Care in Tunisia | Tocilizumab/Deferoxamine | Anti-IL-6 Receptor | RCT | 260 | 3 |
NCT04361552 | Tocilizumab for the Treatment of Cytokine Release Syndrome in Patients With COVID-19 (SARS-CoV-2 Infection) | Tocilizumab | Anti-IL-6 Receptor | RCT | 180 | 3 |
NCT04363736 | A Study to Investigate Intravenous Tocilizumab in Participants With Moderate to Severe COVID-19 Pneumonia | Tocilizumab | Anti-IL-6 Receptor | RCT | 100 | 2 |
NCT04363853 | Tocilizumab Treatment in Patients With COVID-19 | Tocilizumab | Anti-IL-6 Receptor | Single arm | 200 | 2 |
NCT04370834 | Tocilizumab for Patients With Cancer and COVID-19 Disease | Tocilizumab | Anti-IL-6 Receptor | Single arm | 200 | 2 |
NCT04372186 | A Study to Evaluate the Efficacy and Safety of Tocilizumab in Hospitalized Participants With COVID-19 Pneumonia | Tocilizumab | Anti-IL-6 Receptor | RCT | 379 | 3 |
NCT04322773 | Anti-il6 Treatment of Serious COVID-19 Disease with Threatening Respiratory Failure | Tocilizumab + Sarilumab | Anti-IL-6 Receptor | RCT | 200 | 2 |
NCT04345445 | Study to Evaluate the Efficacy and Safety of Tocilizumab Versus Corticosteroids in Hospitalised COVID-19 Patients with High Risk of Progression | Tocilizumab or Corticosteroids | Anti-IL-6 Receptor Glucocorticoid | RCT | 310 | 3 |
NCT04315298 | Evaluation of the Efficacy and Safety of Sarilumab in Hospitalized Patients With COVID-19 | Sarilumab | Anti-IL-6 Receptor | RCT | 400 | 3 |
NCT04324073 | Cohort Multiple Randomized Controlled Trials Open-label of Immune Modulatory Drugs and Other Treatments in COVID-19 Patients - Sarilumab Trial - CORIMUNO-19 - SARI | Sarilumab | Anti-IL-6 Receptor | RCT | 240 | 3 |
NCT04357808 | Efficacy of Subcutaneous Sarilumab in Hospitalised Patients With Moderate-severe COVID-19 Infection (SARCOVID) | Sarilumab | Anti-IL-6 Receptor | RCT | 30 | 2 |
NCT04357860 | Clinical Trial of Sarilumab in Adults With COVID-19 | Sarilumab | Anti-IL-6 Receptor | RCT | 120 | 2 |
NCT04359901 | Sarilumab for Patients With Moderate COVID-19 Disease: A Randomized Controlled Trial With a Play-The-Winner Design | Sarilumab | Anti-IL-6 Receptor | RCT | 120 | 2 |
NCT04322188 | An Observational Case-control Study of the Use of Siltuximab in ARDS Patients Diagnosed With COVID-19 Infection | Siltuximab | Anti-IL-6 | Case-Control | 50 | N/A |
NCT04343989 | A Randomized Placebo-controlled Safety and Dose-finding Study for the Use of the IL-6 Inhibitor Clazakizumab in Patients with Life-threatening COVID-19 Infection | Clazakizumab | Anti-IL-6 | RCT | 30 | 2 |
NCT04348500 | Clazakizumab (Anti-IL- 6 Monoclonal) Compared to Placebo for COVID19 Disease | Clazakizumab | Anti-IL-6 | RCT | 60 | 2 |
NCT04363502 | Use of the Interleukin-6 Inhibitor Clazakizumab in Patients With Life-threatening COVID-19 Infection | Clazakizumab | Anti-IL-6 | RCT | 30 | 2 |
ChiCTR2000030196 | A multicenter, single arm, open label trial for the efficacy and safety of CMAB806 in the treatment of cytokine release syndrome of novel coronavirus pneumonia (COVID-19) | Conventional therapy+ Tocilizumab | Anti-IL-6R | Single arm | 60 | 2 |
NCT04362813 | Study of Efficacy and Safety of Canakinumab Treatment for CRS in Participants With COVID-19-induced Pneumonia | Canakinumab | Anti-IL-1β | RCT | 450 | 3 |
NCT04365153 | Canakinumab to Reduce Deterioration of Cardiac and Respiratory Function Due to COVID-19 | Canakinumab | Anti-IL-1β | RCT | 45 | 2 |
NCT04362111 | Early Identification and Treatment of Cytokine Storm Syndrome in Covid-19 | Anakinra | Anti-IL-1 Receptor | RCT | 20 | 3 |
NCT04357366 | suPAR-guided Anakinra Treatment for Validation of the Risk and Management of Respiratory Failure by COVID-19 (SAVE) | Anakinra or trimethoprim/sulfamethoxazole | Anti-IL-1 Receptor or Anti-inflammation | Single arm | 100 | 2 |
NCT04364009 | Anakinra for COVID-19 Respiratory Symptoms | Anakinra | Anti-IL-1 Receptor | RCT | 240 | 3 |
NCT04366232 | Efficacy of Intravenous Anakinra and Ruxolitinib During COVID-19 Inflammation (JAKINCOV) | Anakinra+ Ruxolitinib | Anti-IL-1 Receptor+ JAK inhibitor | RCT | 50 | 2 |
NCT04330638 | Treatment of COVID-19 Patients with Anti-interleukin Drugs | Anakinra+ Siltuximab+ Tocilizumab | IL-1 receptor Antagonist+ Anti-IL-6+ Anti-IL-6 Receptor | RCT | 342 | 3 |
ChiCTR2000030089 | A clinical study for the efficacy and safety of Adalimumab Injection in the treatment of patients with severe novel coronavirus pneumonia (COVID-19) | Adalimumab | Anti-TNF-alpha | RCT | 60 | 4 |
ChiCTR2000030580 | Efficacy and safety of adamumab combined with tozumab in severe and critical patients with novel coronavirus pneumonia (COVID-19) | Adalimumab and Tocilizumab | Anti-TNF-alpha Anti-IL-6 Receptor | RCT | 60 | 4 |
NCT04324021 | Efficacy and Safety of Emapalumab and Anakinra in Reducing Hyperinflammation and Respiratory Distress in Patients With COVID-19 Infection. | Emapalumab and Anakinra | Anti-IFN-γ IL-1 receptor Antagonist | RCT | 54 | 3 |
ChiCTR2000030703 | A randomized, blinded, controlled, multicenter clinical trial to evaluate the efficacy and safety of Ixekizumab combined with conventional antiviral drugs in patients with novel coronavirus pneumonia (COVID-19) | Ixekizumab | Anti-IL-17A | RCT | 40 | 0 |
NCT04347226 | Anti-Interleukin-8 (Anti-IL-8) for Cancer Patients With COVID-19 | BMS-986253 | Anti-IL-8 | RCT | 138 | 2 |
NCT04275245 | Clinical Study of Anti-CD147 Humanized Meplazumab for Injection to Treat With 2019-nCoV Pneumonia | Humanized Meplazumab | Anti-CD147 | Single arm | 20 | 2 |
NCT04337216 | Mavrilimumab to Reduce Progression of Acute Respiratory Failure in Patients with Severe COVID-19 Pneumonia and Systemic Hyper-inflammation | Mavrilimumab | Anti-GM-CSF-R | Single arm | 10 | 2 |
NCT04341116 | Study of TJ003234 (Anti-GM-CSF Monoclonal Antibody) in Subjects With Severe Coronavirus Disease 2019 (COVID-19) | Anti-GM-CSF Monoclonal Antibody | Anti-GM-CSF | RCT | 144 | 3 |
NCT04343651 | Study to Evaluate the Efficacy and Safety of Leronlimab for Mild to Moderate COVID-19 | Leronlimab | CCR5 blockading | RCT | 75 | 2 |
NCT04347239 | Study to Evaluate the Efficacy and Safety of Leronlimab for Patients With Severe or Critical Coronavirus Disease 2019 (COVID-19) | Leronlimab | CCR5 blockading | RCT | 390 | 2 |
ChiCTR2000030262 | Clinical study for combination of anti-viral drugs and type I interferon and inflammation inhibitor TFF2 in the treatment of novel coronavirus pneumonia (COVID-19) | type I interferon and TFF2 | Boost innate resistance Anti-inflammatory peptide | RCT | 30 | 0 |
ChiCTR2000029572 | Safety and efficacy of umbilical cord blood mononuclear cells in the treatment of severe and critically 2019-nCoV pneumonia (novel coronavirus pneumonia, NCP): a randomized controlled clinical trial | Umbilical cord blood mononuclear cells | Anti-inflammatory, Anti-fibrotic | RCT | 30 | 0 |
ChiCTR2000029606 | Clinical Study for Human Menstrual Blood-Derived Stem Cells in the Treatment of Acute Novel Coronavirus Pneumonia (NCP) | Human Menstrual Blood-Derived Stem Cells | Anti-inflammatory, Anti-fibrotic | RCT | 63 | 0 |
ChiCTR2000029990 | Clinical trials of mesenchymal stem cells for the treatment of pneumonitis caused by novel coronavirus pneumonia (COVID-19) | Mesenchymal stem cells | Anti-inflammatory, Anti-fibrotic | RCT | 120 | 2 |
ChiCTR2000030116 | Safety and effectiveness of human umbilical cord mesenchymal stem cells in the treatment of acute respiratory distress syndrome of severe novel coronavirus pneumonia (COVID-19) | Human umbilical cord mesenchymal stem cells | Anti-inflammatory, Anti-fibrotic | CCT | 16 | N/A |
ChiCTR2000030866 | Open-label, observational study of human umbilical cord derived mesenchymal stem cells in the treatment of severe and critical patients with novel coronavirus pneumonia (COVID-19) | Human umbilical cord derived mesenchymal stem cells | Anti-inflammatory, Anti-fibrotic | Single arm | 30 | 0 |
NCT04299152 | Stem Cell Educator Therapy Treat the Viral Inflammation Caused by Severe Acute Respiratory Syndrome Coronavirus 2 | Stem Cell | Immune suppression | RCT | 20 | 2 |
NCT04333368 | Cell Therapy Using Umbilical Cord-derived Mesenchymal Stromal Cells in SARS-CoV-2-related ARDS | Umbilical Cord-derived Mesenchymal Stromal Cells | Anti-inflammatory, Anti-fibrotic | RCT | 60 | 2 |
NCT04345601 | Mesenchymal Stromal Cells for the Treatment of SARS-CoV-2 Induced Acute Respiratory Failure (COVID-19 Disease) | Mesenchymal Stromal Cells | Anti-inflammatory, Anti-fibrotic | Single arm | 30 | 1 |
NCT04361942 | Treatment of Severe COVID-19 Pneumonia With Allogeneic Mesenchymal Stromal Cells (COVID_MSV) | Allogeneic Mesenchymal Stromal Cells | Anti-inflammatory, Anti-fibrotic | RCT | 24 | 2 |
NCT04366063 | Mesenchymal Stem Cell Therapy for SARS-CoV-2-related Acute Respiratory Distress Syndrome | Mesenchymal Stem Cell | Anti-inflammatory, Anti-fibrotic | RCT | 60 | 3 |
NCT04366830 | Intermediate-size Expanded Access Program (EAP), Mesenchymal Stromal Cells (MSC) for Acute Respiratory Distress Syndrome (ARDS) Due to COVID-19 Infection | EAP+MSCs | Anti-inflammatory, Anti-fibrotic | N/A | N/A | N/A |
NCT04371393 | MSCs in COVID-19 ARDS | MSCs | Anti-inflammatory, Anti-fibrotic | RCT | 300 | 3 |
ChiCTR2000029898 | A Randomized, Open-label, Parallel, Controlled Trial for Evaluation of the Efficacy and Safety of Chloroquine Phosphate in the treatment of Severe Patients with Novel Coronavirus Pneumonia (COVID-19) | Chloroquine Phosphate | Immune suppression | RCT | 100 | 4 |
NCT04323631 | Hydroxychloroquine for the Treatment of Patients with Mild to Moderate COVID-19 to Prevent Progression to Severe Infection or Death | Hydroxychloroquine | Immune suppression | RCT | 1116 | 1 |
NCT04323527 | Chloroquine Diphosphate for the Treatment of Severe Acute Respiratory Syndrome Secondary to SARS-CoV2 | Chloroquine Diphosphate | Immune suppression | RCT | 440 | 2 |
NCT04358068 | Evaluating the Efficacy of Hydroxychloroquine and Azithromycin to Prevent Hospitalization or Death in Persons With COVID-19 | Hydroxychloroquine +Azithromycin | Anti-inflammation | RCT | 2000 | 2 |
NCT04358081 | Hydroxychloroquine Monotherapy and in Combination With Azithromycin in Patients With Moderate and Severe COVID-19 Disease | Hydroxychloroquine+ Monotherapy+ Azithromycin | Anti-inflammation | RCT | 444 | 3 |
NCT04362332 | Chloroquine, Hydroxychloroquine or Only Supportive Care in Patients AdmItted With Moderate to Severe COVID-19 | Chloroquine+ Hydroxychloroquine | Anti-inflammation | RCT | 950 | 4 |
ChiCTR2000029757 | Convalescent plasma for the treatment of severe novel coronavirus pneumonia (COVID-19): a prospective randomized controlled trial | Convalescent plasma | Convalescent plasma | RCT | 200 | 0 |
ChiCTR2000029850 | Study for convalescent plasma treatment for severe patients with novel coronavirus pneumonia (COVID-19) | Convalescent plasma | Convalescent plasma | CCT | 20 | 0 |
ChiCTR2000030010 | A randomized, double-blind, parallel-controlled, trial to evaluate the efficacy and safety of anti-SARS-CoV-2 virus inactivated plasma in the treatment of severe novel coronavirus pneumonia patients (COVID-19) | Anti-SARS-CoV-2 virus inactivated plasma | Convalescent plasma | RCT | 100 | N/A |
ChiCTR2000030929 | A randomized, double-blind, parallel-controlled trial to evaluate the efficacy and safety of anti-SARS-CoV-2 virus inactivated plasma in the treatment of severe novel coronavirus pneumonia (COVID-19) | Anti-SARS-CoV-2 virus inactivated plasma | Convalescent plasma | RCT | 60 | N/A |
NCT04346446 | Efficacy of Convalescent Plasma Therapy in Severely Sick COVID-19 Patients | Convalescent Plasma in severe COVID-19 Patients | Convalescent Plasma | RCT | 20 | 2 |
NCT04347681 | Potential Efficacy of Convalescent Plasma to Treat Severe COVID-19 and Patients at High Risk of Developing Severe COVID-19 | Convalescent Plasma | Convalescent Plasma | CCT | 40 | 2 |
NCT04353206 | Convalescent Plasma in ICU Patients With COVID-19-induced Respiratory Failure | Convalescent Plasma in ICU Patients | Convalescent plasma | Single arm | 90 | 1 |
NCT04359810 | Plasma Therapy of COVID-19 in Critically Ill Patients | Convalescent Plasma | Convalescent plasma | RCT | 105 | 2 |
ChiCTR2000030475 | Cytosorb in Treating Critically Ill Hospitalized Adult Patients with novel coronavirus pneumonia (COVID-19) | Cytosorb | Broad Cytokine/Toxin Removal | Single arm | 19 | 0 |
NCT04324528 | Cytokine Adsorption in Severe COVID-19 Pneumonia Requiring Extracorporeal Membrane Oxygenation | Cytokine Adsorption+ Extracorporeal Membrane Oxygenation | Broad Cytokine/Toxin Removal | Case reports | 30 | R/A |
NCT04344080 | Effect of CytoSorb Adsorber on Hemodynamic and Immunological Parameters in Critical Ill Patients With COVID-19 | CytoSorb | Broad Cytokine/Toxin Removal | RCT | 24 | N/A |
NCT04358003 | Plasma Adsorption in Patients With Confirmed COVID-19 | Plasma Adsorption | Broad Cytokine/Toxin Removal | Single arm | 2000 | N/A |
NCT04374149 | Therapeutic Plasma Exchange Alone or in Combination With Ruxolitinib in COVID-19 Associated CRS | Plasma Exchange | Broad Cytokine/Toxin Removal | CCT | 20 | 2 |
NCT04374539 | Plasma Exchange in Patients With COVID-19 Disease and Invasive Mechanical Ventilation: a Randomized Controlled Trial | Plasma Exchange | Broad Cytokine/Toxin Removal | RCT | 116 | 2 |
NCT04273581 | The Efficacy and Safety of Thalidomide Combined with Low-dose Hormones in the Treatment of Severe COVID-19 | Thalidomide and Interferon-alpha | Prevent lung injury Boost Innate resistance | RCT | 40 | 2 |
NCT04293887 | Efficacy and Safety of IFN-α2β in the Treatment of Novel Coronavirus Patients | IFN-α2β | Boost Innate Resistance | RCT | 328 | 1 |
NCT04343768 | An Investigation into Beneficial Effects of Interferon Beta 1a, Compared to Interferon Beta 1b And The Base Therapeutic Regiment in Moderate to Severe COVID-19: A Randomized Clinical Trial | Interferon Beta 1a or Interferon Beta 1b | Boost Innate Resistance | RCT | 60 | 4 |
NCT04325061 | Efficacy of Dexamethasone Treatment for Patients with ARDS Caused by COVID-19 | Dexamethasone | Anti-inflammatory | RCT | 200 | 4 |
NCT04347980 | Dexamethasone Treatment for Severe Acute Respiratory Distress Syndrome Induced by COVID-19 | Dexamethasone | Anti-inflammatory | RCT | 122 | 3 |
NCT04327401 | COVID-19-associated ARDS Treated with Dexamethasone: Alliance Covid-19 Brasil III | Dexamethasone | Immune Suppression | RCT | 290 | 3 |
NCT04358627 | Dexmedetomidine to Improve Outcomes of ARDS in Critical Care COVID-19 Patients | Dexmedetomidine | Immune Suppression | Case | 80 | N/A |
NCT04355247 | Prophylactic Corticosteroid to Prevent COVID-19 Cytokine Storm | Corticosteroid | Immune Suppression | Single arm | 20 | 2 |
NCT04360876 | Targeted Steroids for ARDS Due to COVID-19 Pneumonia: A Pilot Randomized Clinical Trial | Steroids | Immune Suppression | RCT | 90 | 2 |
NCT04323592 | Efficacy of Methylprednisolone for Patients With COVID-19 Severe Acute Respiratory Syndrome | Methylprednisolone | Anti-inflammatory | CCT | 104 | 3 |
NCT04343729 | Methylprednisolone in the Treatment of Patients with Signs of Severe Acute Respiratory Syndrome in Covid-19 | Methylprednisolone | Anti-inflammatory | RCT | 420 | 2 |
NCT04306393 | Nitric Oxide Gas Inhalation in Severe Acute Respiratory Syndrome in COVID-19 | Nitric Oxide Gas | Pulmonary vasodilator | RCT | 200 | 2 |
NCT04358588 | Pulsed Inhaled Nitric Oxide for the Treatment of Patients With Mild or Moderate COVID-19 | Nitric Oxide | Anti-inflammation | N/A | N/A | N/A |
NCT04244591 | Glucocorticoid Therapy for Novel Coronavirus Critically Ill Patients With Severe Acute Respiratory Failure | Glucocorticoid | Immune suppression | RCT | 80 | 3 |
NCT04320277 | Baricitinib in Symptomatic Patients Infected by COVID-19: an Open-label, Pilot Study. | Baricitinib | JAK inhibitor | CCT | 60 | 3 |
NCT04340232 | Safety and Efficacy of Baricitinib for COVID-19 | Baricitinib | JAK inhibitor | Single arm | 80 | 3 |
NCT04359290 | Ruxolitinib for Treatment of Covid-19 Induced Lung Injury ARDS | Ruxolitinib | JAK inhibitor | Single arm | 15 | 2 |
NCT04355793 | Expanded Access Program of Ruxolitinib for the Emergency Treatment of Cytokine Storm From COVID-19 Infection | Ruxolitinib | JAK inhibitor | N/A | N/A | N/A |
NCT04361903 | Ruxolitinib for the Treatment of Acute Respiratory Distress Syndrome in Patients With COVID-19 Infection | Ruxolitinib | JAK inhibitor | Cohort | 13 | N/A |
NCT04362137 | Phase 3 Randomized, Double-blind, Placebo-controlled Multi-center Study to Assess the Efficacy and Safety of Ruxolitinib in Patients With COVID-19 Associated Cytokine Storm (RUXCOVID) | Ruxolitinib | JAK inhibitor | RCT | 402 | 3 |
NCT04321993 | Treatment of Moderate to Severe Coronavirus Disease (COVID-19) in Hospitalized Patients | Baricitinib+ Sarilumab+Lopinavir/ritonavir+Hydroxychloroquine sulfate | JAK inhibitor+ Anti-IL-6+ Anti-virus+ Anti-inflammatory | CCT | 1000 | 2 |
NCT04373044 | Antiviral Therapy and Baricitinib for the Treatment of Patients With Moderate or Severe COVID-19 | Antiviral Therapy+Baricitinib | Anti-virus+JAK inhibitor | Single arm | 59 | 2 |
NCT04348383 | Defibrotide as Prevention and Treatment of Respiratory Distress and Cytokine Release Syndrome of Covid 19. | Defibrotide | Anti-inflammatory | RCT | 120 | 2 |
NCT04357444 | Low Dose of IL-2 In Acute Respiratory DistrEss Syndrome Related to COVID-19 | IL-2 | Anti-inflammation | RCT | 30 | 2 |
NCT04355364 | Efficacy and Safety of Aerosolized Intra-tracheal Dornase Alpha Administration in Patients With COVID19-induced ARDS (COVIDORNASE) | Aerosolized Intra-tracheal Dornase Alpha | Anti-inflammation | RCT | 100 | 3 |
NCT04363437 | COlchicine in Moderate Severity Hospitalized Patients Before ARDS to Treat COVID-19 | Colchicine | Anti-inflammation | RCT | 70 | 2 |
NCT04366791 | Radiation Eliminates Storming Cytokines and Unchecked Edema as a 1-Day Treatment for COVID-19 | Radiation | Other | Single arm | 10 | 2 |
Register Number . | Title . | Drugs/Strategies . | Therapeutic Target . | Study design . | Samples . | Phase . |
---|---|---|---|---|---|---|
ChiCTR2000029765 | A multicenter, randomized controlled trial for the efficacy and safety of tocilizumab in the treatment of new coronavirus pneumonia (COVID-19) | Tocilizumab | Anti-IL-6 Receptor | RCT | 188 | 4 |
ChiCTR2000030196 | A multicenter, single arm, open label trial for the efficacy and safety of CMAB806 in the treatment of cytokine release syndrome of novel coronavirus pneumonia (COVID-19) | Tocilizumab | Anti-IL-6 Receptor | Single arm | 60 | 2 |
NCT04317092 | Tocilizumab in COVID-19 Pneumonia (TOCIVID-19) | Tocilizumab | Anti-IL-6 Receptor | Single arm | 330 | 2 |
NCT04320615 | A Study to Evaluate the Safety and Efficacy of Tocilizumab in Patients with Severe COVID-19 Pneumonia | Tocilizumab | Anti-IL-6 Receptor | RCT | 330 | 3 |
NCT04310228 | Favipiravir Combined with Tocilizumab in the Treatment of Corona Virus Disease 2019 | Tocilizumab | Anti-IL-6 Receptor | RCT | 150 | N/A |
NCT04306705 | Tocilizumab vs CRRT in Management of Cytokine Release Syndrome (CRS) in COVID-19 | Tocilizumab | Anti-IL-6 Receptor | Cohort study | 120 | N/A |
NCT04315480 | Tocilizumab for SARS-CoV2 Severe Pneumonitis | Tocilizumab | Anti-IL-6 Receptor | Single arm | 30 | 2 |
NCT04331795 | Tocilizumab to Prevent Clinical Decompensation in Hospitalized, Non-critically Ill Patients With COVID-19 Pneumonitis | Tocilizumab | Anti-IL-6 Receptor | RCT | 50 | 2 |
NCT04331808 | CORIMUNO-19 - Tocilizumab Trial - TOCI (CORIMUNO-TOCI) | Tocilizumab | Anti-IL-6 Receptor | RCT | 240 | 2 |
NCT04332913 | Efficacy and Safety of Tocilizumab in the Treatment of SARS-Cov-2 Related Pneumonia | Tocilizumab | Anti-IL-6 Receptor | Cohort study | 30 | N/A |
NCT04335071 | Tocilizumab in the Treatment of Coronavirus Induced Disease (COVID-19) | Tocilizumab | Anti-IL-6 Receptor | RCT | 100 | 2 |
NCT04346355 | Efficacy of Early Administration of Tocilizumab in COVID-19 Patients | Tocilizumab | Anti-IL-6 Receptor | RCT | 398 | 2 |
NCT04356937 | Efficacy of Tocilizumab on Patients With COVID-19 | Tocilizumab | Anti-IL-6 Receptor | RCT | 300 | 3 |
NCT04359667 | Serum IL-6 and Soluble IL-6 Receptor in Severe COVID-19 Pneumonia Treated With Tocilizumab | Tocilizumab | Anti-IL-6 Receptor | Case | 30 | N/A |
NCT04361032 | Assessment of Efficacy and Safety of Tocilizumab Compared to Deferoxamine, Associated With Standards Treatments in COVID-19 (+) Patients Hospitalized In Intensive Care in Tunisia | Tocilizumab/Deferoxamine | Anti-IL-6 Receptor | RCT | 260 | 3 |
NCT04361552 | Tocilizumab for the Treatment of Cytokine Release Syndrome in Patients With COVID-19 (SARS-CoV-2 Infection) | Tocilizumab | Anti-IL-6 Receptor | RCT | 180 | 3 |
NCT04363736 | A Study to Investigate Intravenous Tocilizumab in Participants With Moderate to Severe COVID-19 Pneumonia | Tocilizumab | Anti-IL-6 Receptor | RCT | 100 | 2 |
NCT04363853 | Tocilizumab Treatment in Patients With COVID-19 | Tocilizumab | Anti-IL-6 Receptor | Single arm | 200 | 2 |
NCT04370834 | Tocilizumab for Patients With Cancer and COVID-19 Disease | Tocilizumab | Anti-IL-6 Receptor | Single arm | 200 | 2 |
NCT04372186 | A Study to Evaluate the Efficacy and Safety of Tocilizumab in Hospitalized Participants With COVID-19 Pneumonia | Tocilizumab | Anti-IL-6 Receptor | RCT | 379 | 3 |
NCT04322773 | Anti-il6 Treatment of Serious COVID-19 Disease with Threatening Respiratory Failure | Tocilizumab + Sarilumab | Anti-IL-6 Receptor | RCT | 200 | 2 |
NCT04345445 | Study to Evaluate the Efficacy and Safety of Tocilizumab Versus Corticosteroids in Hospitalised COVID-19 Patients with High Risk of Progression | Tocilizumab or Corticosteroids | Anti-IL-6 Receptor Glucocorticoid | RCT | 310 | 3 |
NCT04315298 | Evaluation of the Efficacy and Safety of Sarilumab in Hospitalized Patients With COVID-19 | Sarilumab | Anti-IL-6 Receptor | RCT | 400 | 3 |
NCT04324073 | Cohort Multiple Randomized Controlled Trials Open-label of Immune Modulatory Drugs and Other Treatments in COVID-19 Patients - Sarilumab Trial - CORIMUNO-19 - SARI | Sarilumab | Anti-IL-6 Receptor | RCT | 240 | 3 |
NCT04357808 | Efficacy of Subcutaneous Sarilumab in Hospitalised Patients With Moderate-severe COVID-19 Infection (SARCOVID) | Sarilumab | Anti-IL-6 Receptor | RCT | 30 | 2 |
NCT04357860 | Clinical Trial of Sarilumab in Adults With COVID-19 | Sarilumab | Anti-IL-6 Receptor | RCT | 120 | 2 |
NCT04359901 | Sarilumab for Patients With Moderate COVID-19 Disease: A Randomized Controlled Trial With a Play-The-Winner Design | Sarilumab | Anti-IL-6 Receptor | RCT | 120 | 2 |
NCT04322188 | An Observational Case-control Study of the Use of Siltuximab in ARDS Patients Diagnosed With COVID-19 Infection | Siltuximab | Anti-IL-6 | Case-Control | 50 | N/A |
NCT04343989 | A Randomized Placebo-controlled Safety and Dose-finding Study for the Use of the IL-6 Inhibitor Clazakizumab in Patients with Life-threatening COVID-19 Infection | Clazakizumab | Anti-IL-6 | RCT | 30 | 2 |
NCT04348500 | Clazakizumab (Anti-IL- 6 Monoclonal) Compared to Placebo for COVID19 Disease | Clazakizumab | Anti-IL-6 | RCT | 60 | 2 |
NCT04363502 | Use of the Interleukin-6 Inhibitor Clazakizumab in Patients With Life-threatening COVID-19 Infection | Clazakizumab | Anti-IL-6 | RCT | 30 | 2 |
ChiCTR2000030196 | A multicenter, single arm, open label trial for the efficacy and safety of CMAB806 in the treatment of cytokine release syndrome of novel coronavirus pneumonia (COVID-19) | Conventional therapy+ Tocilizumab | Anti-IL-6R | Single arm | 60 | 2 |
NCT04362813 | Study of Efficacy and Safety of Canakinumab Treatment for CRS in Participants With COVID-19-induced Pneumonia | Canakinumab | Anti-IL-1β | RCT | 450 | 3 |
NCT04365153 | Canakinumab to Reduce Deterioration of Cardiac and Respiratory Function Due to COVID-19 | Canakinumab | Anti-IL-1β | RCT | 45 | 2 |
NCT04362111 | Early Identification and Treatment of Cytokine Storm Syndrome in Covid-19 | Anakinra | Anti-IL-1 Receptor | RCT | 20 | 3 |
NCT04357366 | suPAR-guided Anakinra Treatment for Validation of the Risk and Management of Respiratory Failure by COVID-19 (SAVE) | Anakinra or trimethoprim/sulfamethoxazole | Anti-IL-1 Receptor or Anti-inflammation | Single arm | 100 | 2 |
NCT04364009 | Anakinra for COVID-19 Respiratory Symptoms | Anakinra | Anti-IL-1 Receptor | RCT | 240 | 3 |
NCT04366232 | Efficacy of Intravenous Anakinra and Ruxolitinib During COVID-19 Inflammation (JAKINCOV) | Anakinra+ Ruxolitinib | Anti-IL-1 Receptor+ JAK inhibitor | RCT | 50 | 2 |
NCT04330638 | Treatment of COVID-19 Patients with Anti-interleukin Drugs | Anakinra+ Siltuximab+ Tocilizumab | IL-1 receptor Antagonist+ Anti-IL-6+ Anti-IL-6 Receptor | RCT | 342 | 3 |
ChiCTR2000030089 | A clinical study for the efficacy and safety of Adalimumab Injection in the treatment of patients with severe novel coronavirus pneumonia (COVID-19) | Adalimumab | Anti-TNF-alpha | RCT | 60 | 4 |
ChiCTR2000030580 | Efficacy and safety of adamumab combined with tozumab in severe and critical patients with novel coronavirus pneumonia (COVID-19) | Adalimumab and Tocilizumab | Anti-TNF-alpha Anti-IL-6 Receptor | RCT | 60 | 4 |
NCT04324021 | Efficacy and Safety of Emapalumab and Anakinra in Reducing Hyperinflammation and Respiratory Distress in Patients With COVID-19 Infection. | Emapalumab and Anakinra | Anti-IFN-γ IL-1 receptor Antagonist | RCT | 54 | 3 |
ChiCTR2000030703 | A randomized, blinded, controlled, multicenter clinical trial to evaluate the efficacy and safety of Ixekizumab combined with conventional antiviral drugs in patients with novel coronavirus pneumonia (COVID-19) | Ixekizumab | Anti-IL-17A | RCT | 40 | 0 |
NCT04347226 | Anti-Interleukin-8 (Anti-IL-8) for Cancer Patients With COVID-19 | BMS-986253 | Anti-IL-8 | RCT | 138 | 2 |
NCT04275245 | Clinical Study of Anti-CD147 Humanized Meplazumab for Injection to Treat With 2019-nCoV Pneumonia | Humanized Meplazumab | Anti-CD147 | Single arm | 20 | 2 |
NCT04337216 | Mavrilimumab to Reduce Progression of Acute Respiratory Failure in Patients with Severe COVID-19 Pneumonia and Systemic Hyper-inflammation | Mavrilimumab | Anti-GM-CSF-R | Single arm | 10 | 2 |
NCT04341116 | Study of TJ003234 (Anti-GM-CSF Monoclonal Antibody) in Subjects With Severe Coronavirus Disease 2019 (COVID-19) | Anti-GM-CSF Monoclonal Antibody | Anti-GM-CSF | RCT | 144 | 3 |
NCT04343651 | Study to Evaluate the Efficacy and Safety of Leronlimab for Mild to Moderate COVID-19 | Leronlimab | CCR5 blockading | RCT | 75 | 2 |
NCT04347239 | Study to Evaluate the Efficacy and Safety of Leronlimab for Patients With Severe or Critical Coronavirus Disease 2019 (COVID-19) | Leronlimab | CCR5 blockading | RCT | 390 | 2 |
ChiCTR2000030262 | Clinical study for combination of anti-viral drugs and type I interferon and inflammation inhibitor TFF2 in the treatment of novel coronavirus pneumonia (COVID-19) | type I interferon and TFF2 | Boost innate resistance Anti-inflammatory peptide | RCT | 30 | 0 |
ChiCTR2000029572 | Safety and efficacy of umbilical cord blood mononuclear cells in the treatment of severe and critically 2019-nCoV pneumonia (novel coronavirus pneumonia, NCP): a randomized controlled clinical trial | Umbilical cord blood mononuclear cells | Anti-inflammatory, Anti-fibrotic | RCT | 30 | 0 |
ChiCTR2000029606 | Clinical Study for Human Menstrual Blood-Derived Stem Cells in the Treatment of Acute Novel Coronavirus Pneumonia (NCP) | Human Menstrual Blood-Derived Stem Cells | Anti-inflammatory, Anti-fibrotic | RCT | 63 | 0 |
ChiCTR2000029990 | Clinical trials of mesenchymal stem cells for the treatment of pneumonitis caused by novel coronavirus pneumonia (COVID-19) | Mesenchymal stem cells | Anti-inflammatory, Anti-fibrotic | RCT | 120 | 2 |
ChiCTR2000030116 | Safety and effectiveness of human umbilical cord mesenchymal stem cells in the treatment of acute respiratory distress syndrome of severe novel coronavirus pneumonia (COVID-19) | Human umbilical cord mesenchymal stem cells | Anti-inflammatory, Anti-fibrotic | CCT | 16 | N/A |
ChiCTR2000030866 | Open-label, observational study of human umbilical cord derived mesenchymal stem cells in the treatment of severe and critical patients with novel coronavirus pneumonia (COVID-19) | Human umbilical cord derived mesenchymal stem cells | Anti-inflammatory, Anti-fibrotic | Single arm | 30 | 0 |
NCT04299152 | Stem Cell Educator Therapy Treat the Viral Inflammation Caused by Severe Acute Respiratory Syndrome Coronavirus 2 | Stem Cell | Immune suppression | RCT | 20 | 2 |
NCT04333368 | Cell Therapy Using Umbilical Cord-derived Mesenchymal Stromal Cells in SARS-CoV-2-related ARDS | Umbilical Cord-derived Mesenchymal Stromal Cells | Anti-inflammatory, Anti-fibrotic | RCT | 60 | 2 |
NCT04345601 | Mesenchymal Stromal Cells for the Treatment of SARS-CoV-2 Induced Acute Respiratory Failure (COVID-19 Disease) | Mesenchymal Stromal Cells | Anti-inflammatory, Anti-fibrotic | Single arm | 30 | 1 |
NCT04361942 | Treatment of Severe COVID-19 Pneumonia With Allogeneic Mesenchymal Stromal Cells (COVID_MSV) | Allogeneic Mesenchymal Stromal Cells | Anti-inflammatory, Anti-fibrotic | RCT | 24 | 2 |
NCT04366063 | Mesenchymal Stem Cell Therapy for SARS-CoV-2-related Acute Respiratory Distress Syndrome | Mesenchymal Stem Cell | Anti-inflammatory, Anti-fibrotic | RCT | 60 | 3 |
NCT04366830 | Intermediate-size Expanded Access Program (EAP), Mesenchymal Stromal Cells (MSC) for Acute Respiratory Distress Syndrome (ARDS) Due to COVID-19 Infection | EAP+MSCs | Anti-inflammatory, Anti-fibrotic | N/A | N/A | N/A |
NCT04371393 | MSCs in COVID-19 ARDS | MSCs | Anti-inflammatory, Anti-fibrotic | RCT | 300 | 3 |
ChiCTR2000029898 | A Randomized, Open-label, Parallel, Controlled Trial for Evaluation of the Efficacy and Safety of Chloroquine Phosphate in the treatment of Severe Patients with Novel Coronavirus Pneumonia (COVID-19) | Chloroquine Phosphate | Immune suppression | RCT | 100 | 4 |
NCT04323631 | Hydroxychloroquine for the Treatment of Patients with Mild to Moderate COVID-19 to Prevent Progression to Severe Infection or Death | Hydroxychloroquine | Immune suppression | RCT | 1116 | 1 |
NCT04323527 | Chloroquine Diphosphate for the Treatment of Severe Acute Respiratory Syndrome Secondary to SARS-CoV2 | Chloroquine Diphosphate | Immune suppression | RCT | 440 | 2 |
NCT04358068 | Evaluating the Efficacy of Hydroxychloroquine and Azithromycin to Prevent Hospitalization or Death in Persons With COVID-19 | Hydroxychloroquine +Azithromycin | Anti-inflammation | RCT | 2000 | 2 |
NCT04358081 | Hydroxychloroquine Monotherapy and in Combination With Azithromycin in Patients With Moderate and Severe COVID-19 Disease | Hydroxychloroquine+ Monotherapy+ Azithromycin | Anti-inflammation | RCT | 444 | 3 |
NCT04362332 | Chloroquine, Hydroxychloroquine or Only Supportive Care in Patients AdmItted With Moderate to Severe COVID-19 | Chloroquine+ Hydroxychloroquine | Anti-inflammation | RCT | 950 | 4 |
ChiCTR2000029757 | Convalescent plasma for the treatment of severe novel coronavirus pneumonia (COVID-19): a prospective randomized controlled trial | Convalescent plasma | Convalescent plasma | RCT | 200 | 0 |
ChiCTR2000029850 | Study for convalescent plasma treatment for severe patients with novel coronavirus pneumonia (COVID-19) | Convalescent plasma | Convalescent plasma | CCT | 20 | 0 |
ChiCTR2000030010 | A randomized, double-blind, parallel-controlled, trial to evaluate the efficacy and safety of anti-SARS-CoV-2 virus inactivated plasma in the treatment of severe novel coronavirus pneumonia patients (COVID-19) | Anti-SARS-CoV-2 virus inactivated plasma | Convalescent plasma | RCT | 100 | N/A |
ChiCTR2000030929 | A randomized, double-blind, parallel-controlled trial to evaluate the efficacy and safety of anti-SARS-CoV-2 virus inactivated plasma in the treatment of severe novel coronavirus pneumonia (COVID-19) | Anti-SARS-CoV-2 virus inactivated plasma | Convalescent plasma | RCT | 60 | N/A |
NCT04346446 | Efficacy of Convalescent Plasma Therapy in Severely Sick COVID-19 Patients | Convalescent Plasma in severe COVID-19 Patients | Convalescent Plasma | RCT | 20 | 2 |
NCT04347681 | Potential Efficacy of Convalescent Plasma to Treat Severe COVID-19 and Patients at High Risk of Developing Severe COVID-19 | Convalescent Plasma | Convalescent Plasma | CCT | 40 | 2 |
NCT04353206 | Convalescent Plasma in ICU Patients With COVID-19-induced Respiratory Failure | Convalescent Plasma in ICU Patients | Convalescent plasma | Single arm | 90 | 1 |
NCT04359810 | Plasma Therapy of COVID-19 in Critically Ill Patients | Convalescent Plasma | Convalescent plasma | RCT | 105 | 2 |
ChiCTR2000030475 | Cytosorb in Treating Critically Ill Hospitalized Adult Patients with novel coronavirus pneumonia (COVID-19) | Cytosorb | Broad Cytokine/Toxin Removal | Single arm | 19 | 0 |
NCT04324528 | Cytokine Adsorption in Severe COVID-19 Pneumonia Requiring Extracorporeal Membrane Oxygenation | Cytokine Adsorption+ Extracorporeal Membrane Oxygenation | Broad Cytokine/Toxin Removal | Case reports | 30 | R/A |
NCT04344080 | Effect of CytoSorb Adsorber on Hemodynamic and Immunological Parameters in Critical Ill Patients With COVID-19 | CytoSorb | Broad Cytokine/Toxin Removal | RCT | 24 | N/A |
NCT04358003 | Plasma Adsorption in Patients With Confirmed COVID-19 | Plasma Adsorption | Broad Cytokine/Toxin Removal | Single arm | 2000 | N/A |
NCT04374149 | Therapeutic Plasma Exchange Alone or in Combination With Ruxolitinib in COVID-19 Associated CRS | Plasma Exchange | Broad Cytokine/Toxin Removal | CCT | 20 | 2 |
NCT04374539 | Plasma Exchange in Patients With COVID-19 Disease and Invasive Mechanical Ventilation: a Randomized Controlled Trial | Plasma Exchange | Broad Cytokine/Toxin Removal | RCT | 116 | 2 |
NCT04273581 | The Efficacy and Safety of Thalidomide Combined with Low-dose Hormones in the Treatment of Severe COVID-19 | Thalidomide and Interferon-alpha | Prevent lung injury Boost Innate resistance | RCT | 40 | 2 |
NCT04293887 | Efficacy and Safety of IFN-α2β in the Treatment of Novel Coronavirus Patients | IFN-α2β | Boost Innate Resistance | RCT | 328 | 1 |
NCT04343768 | An Investigation into Beneficial Effects of Interferon Beta 1a, Compared to Interferon Beta 1b And The Base Therapeutic Regiment in Moderate to Severe COVID-19: A Randomized Clinical Trial | Interferon Beta 1a or Interferon Beta 1b | Boost Innate Resistance | RCT | 60 | 4 |
NCT04325061 | Efficacy of Dexamethasone Treatment for Patients with ARDS Caused by COVID-19 | Dexamethasone | Anti-inflammatory | RCT | 200 | 4 |
NCT04347980 | Dexamethasone Treatment for Severe Acute Respiratory Distress Syndrome Induced by COVID-19 | Dexamethasone | Anti-inflammatory | RCT | 122 | 3 |
NCT04327401 | COVID-19-associated ARDS Treated with Dexamethasone: Alliance Covid-19 Brasil III | Dexamethasone | Immune Suppression | RCT | 290 | 3 |
NCT04358627 | Dexmedetomidine to Improve Outcomes of ARDS in Critical Care COVID-19 Patients | Dexmedetomidine | Immune Suppression | Case | 80 | N/A |
NCT04355247 | Prophylactic Corticosteroid to Prevent COVID-19 Cytokine Storm | Corticosteroid | Immune Suppression | Single arm | 20 | 2 |
NCT04360876 | Targeted Steroids for ARDS Due to COVID-19 Pneumonia: A Pilot Randomized Clinical Trial | Steroids | Immune Suppression | RCT | 90 | 2 |
NCT04323592 | Efficacy of Methylprednisolone for Patients With COVID-19 Severe Acute Respiratory Syndrome | Methylprednisolone | Anti-inflammatory | CCT | 104 | 3 |
NCT04343729 | Methylprednisolone in the Treatment of Patients with Signs of Severe Acute Respiratory Syndrome in Covid-19 | Methylprednisolone | Anti-inflammatory | RCT | 420 | 2 |
NCT04306393 | Nitric Oxide Gas Inhalation in Severe Acute Respiratory Syndrome in COVID-19 | Nitric Oxide Gas | Pulmonary vasodilator | RCT | 200 | 2 |
NCT04358588 | Pulsed Inhaled Nitric Oxide for the Treatment of Patients With Mild or Moderate COVID-19 | Nitric Oxide | Anti-inflammation | N/A | N/A | N/A |
NCT04244591 | Glucocorticoid Therapy for Novel Coronavirus Critically Ill Patients With Severe Acute Respiratory Failure | Glucocorticoid | Immune suppression | RCT | 80 | 3 |
NCT04320277 | Baricitinib in Symptomatic Patients Infected by COVID-19: an Open-label, Pilot Study. | Baricitinib | JAK inhibitor | CCT | 60 | 3 |
NCT04340232 | Safety and Efficacy of Baricitinib for COVID-19 | Baricitinib | JAK inhibitor | Single arm | 80 | 3 |
NCT04359290 | Ruxolitinib for Treatment of Covid-19 Induced Lung Injury ARDS | Ruxolitinib | JAK inhibitor | Single arm | 15 | 2 |
NCT04355793 | Expanded Access Program of Ruxolitinib for the Emergency Treatment of Cytokine Storm From COVID-19 Infection | Ruxolitinib | JAK inhibitor | N/A | N/A | N/A |
NCT04361903 | Ruxolitinib for the Treatment of Acute Respiratory Distress Syndrome in Patients With COVID-19 Infection | Ruxolitinib | JAK inhibitor | Cohort | 13 | N/A |
NCT04362137 | Phase 3 Randomized, Double-blind, Placebo-controlled Multi-center Study to Assess the Efficacy and Safety of Ruxolitinib in Patients With COVID-19 Associated Cytokine Storm (RUXCOVID) | Ruxolitinib | JAK inhibitor | RCT | 402 | 3 |
NCT04321993 | Treatment of Moderate to Severe Coronavirus Disease (COVID-19) in Hospitalized Patients | Baricitinib+ Sarilumab+Lopinavir/ritonavir+Hydroxychloroquine sulfate | JAK inhibitor+ Anti-IL-6+ Anti-virus+ Anti-inflammatory | CCT | 1000 | 2 |
NCT04373044 | Antiviral Therapy and Baricitinib for the Treatment of Patients With Moderate or Severe COVID-19 | Antiviral Therapy+Baricitinib | Anti-virus+JAK inhibitor | Single arm | 59 | 2 |
NCT04348383 | Defibrotide as Prevention and Treatment of Respiratory Distress and Cytokine Release Syndrome of Covid 19. | Defibrotide | Anti-inflammatory | RCT | 120 | 2 |
NCT04357444 | Low Dose of IL-2 In Acute Respiratory DistrEss Syndrome Related to COVID-19 | IL-2 | Anti-inflammation | RCT | 30 | 2 |
NCT04355364 | Efficacy and Safety of Aerosolized Intra-tracheal Dornase Alpha Administration in Patients With COVID19-induced ARDS (COVIDORNASE) | Aerosolized Intra-tracheal Dornase Alpha | Anti-inflammation | RCT | 100 | 3 |
NCT04363437 | COlchicine in Moderate Severity Hospitalized Patients Before ARDS to Treat COVID-19 | Colchicine | Anti-inflammation | RCT | 70 | 2 |
NCT04366791 | Radiation Eliminates Storming Cytokines and Unchecked Edema as a 1-Day Treatment for COVID-19 | Radiation | Other | Single arm | 10 | 2 |
Abbrevation: ChiCTR, Chinese Clinical Trials Register; NCT, National Clinical Trails; RCT: Random clinical trial; CCT: Controlled clinical trial;
Ongoing Clinical Trials: therapeutics against cytokine storm (up to May 6, 2020)
Register Number . | Title . | Drugs/Strategies . | Therapeutic Target . | Study design . | Samples . | Phase . |
---|---|---|---|---|---|---|
ChiCTR2000029765 | A multicenter, randomized controlled trial for the efficacy and safety of tocilizumab in the treatment of new coronavirus pneumonia (COVID-19) | Tocilizumab | Anti-IL-6 Receptor | RCT | 188 | 4 |
ChiCTR2000030196 | A multicenter, single arm, open label trial for the efficacy and safety of CMAB806 in the treatment of cytokine release syndrome of novel coronavirus pneumonia (COVID-19) | Tocilizumab | Anti-IL-6 Receptor | Single arm | 60 | 2 |
NCT04317092 | Tocilizumab in COVID-19 Pneumonia (TOCIVID-19) | Tocilizumab | Anti-IL-6 Receptor | Single arm | 330 | 2 |
NCT04320615 | A Study to Evaluate the Safety and Efficacy of Tocilizumab in Patients with Severe COVID-19 Pneumonia | Tocilizumab | Anti-IL-6 Receptor | RCT | 330 | 3 |
NCT04310228 | Favipiravir Combined with Tocilizumab in the Treatment of Corona Virus Disease 2019 | Tocilizumab | Anti-IL-6 Receptor | RCT | 150 | N/A |
NCT04306705 | Tocilizumab vs CRRT in Management of Cytokine Release Syndrome (CRS) in COVID-19 | Tocilizumab | Anti-IL-6 Receptor | Cohort study | 120 | N/A |
NCT04315480 | Tocilizumab for SARS-CoV2 Severe Pneumonitis | Tocilizumab | Anti-IL-6 Receptor | Single arm | 30 | 2 |
NCT04331795 | Tocilizumab to Prevent Clinical Decompensation in Hospitalized, Non-critically Ill Patients With COVID-19 Pneumonitis | Tocilizumab | Anti-IL-6 Receptor | RCT | 50 | 2 |
NCT04331808 | CORIMUNO-19 - Tocilizumab Trial - TOCI (CORIMUNO-TOCI) | Tocilizumab | Anti-IL-6 Receptor | RCT | 240 | 2 |
NCT04332913 | Efficacy and Safety of Tocilizumab in the Treatment of SARS-Cov-2 Related Pneumonia | Tocilizumab | Anti-IL-6 Receptor | Cohort study | 30 | N/A |
NCT04335071 | Tocilizumab in the Treatment of Coronavirus Induced Disease (COVID-19) | Tocilizumab | Anti-IL-6 Receptor | RCT | 100 | 2 |
NCT04346355 | Efficacy of Early Administration of Tocilizumab in COVID-19 Patients | Tocilizumab | Anti-IL-6 Receptor | RCT | 398 | 2 |
NCT04356937 | Efficacy of Tocilizumab on Patients With COVID-19 | Tocilizumab | Anti-IL-6 Receptor | RCT | 300 | 3 |
NCT04359667 | Serum IL-6 and Soluble IL-6 Receptor in Severe COVID-19 Pneumonia Treated With Tocilizumab | Tocilizumab | Anti-IL-6 Receptor | Case | 30 | N/A |
NCT04361032 | Assessment of Efficacy and Safety of Tocilizumab Compared to Deferoxamine, Associated With Standards Treatments in COVID-19 (+) Patients Hospitalized In Intensive Care in Tunisia | Tocilizumab/Deferoxamine | Anti-IL-6 Receptor | RCT | 260 | 3 |
NCT04361552 | Tocilizumab for the Treatment of Cytokine Release Syndrome in Patients With COVID-19 (SARS-CoV-2 Infection) | Tocilizumab | Anti-IL-6 Receptor | RCT | 180 | 3 |
NCT04363736 | A Study to Investigate Intravenous Tocilizumab in Participants With Moderate to Severe COVID-19 Pneumonia | Tocilizumab | Anti-IL-6 Receptor | RCT | 100 | 2 |
NCT04363853 | Tocilizumab Treatment in Patients With COVID-19 | Tocilizumab | Anti-IL-6 Receptor | Single arm | 200 | 2 |
NCT04370834 | Tocilizumab for Patients With Cancer and COVID-19 Disease | Tocilizumab | Anti-IL-6 Receptor | Single arm | 200 | 2 |
NCT04372186 | A Study to Evaluate the Efficacy and Safety of Tocilizumab in Hospitalized Participants With COVID-19 Pneumonia | Tocilizumab | Anti-IL-6 Receptor | RCT | 379 | 3 |
NCT04322773 | Anti-il6 Treatment of Serious COVID-19 Disease with Threatening Respiratory Failure | Tocilizumab + Sarilumab | Anti-IL-6 Receptor | RCT | 200 | 2 |
NCT04345445 | Study to Evaluate the Efficacy and Safety of Tocilizumab Versus Corticosteroids in Hospitalised COVID-19 Patients with High Risk of Progression | Tocilizumab or Corticosteroids | Anti-IL-6 Receptor Glucocorticoid | RCT | 310 | 3 |
NCT04315298 | Evaluation of the Efficacy and Safety of Sarilumab in Hospitalized Patients With COVID-19 | Sarilumab | Anti-IL-6 Receptor | RCT | 400 | 3 |
NCT04324073 | Cohort Multiple Randomized Controlled Trials Open-label of Immune Modulatory Drugs and Other Treatments in COVID-19 Patients - Sarilumab Trial - CORIMUNO-19 - SARI | Sarilumab | Anti-IL-6 Receptor | RCT | 240 | 3 |
NCT04357808 | Efficacy of Subcutaneous Sarilumab in Hospitalised Patients With Moderate-severe COVID-19 Infection (SARCOVID) | Sarilumab | Anti-IL-6 Receptor | RCT | 30 | 2 |
NCT04357860 | Clinical Trial of Sarilumab in Adults With COVID-19 | Sarilumab | Anti-IL-6 Receptor | RCT | 120 | 2 |
NCT04359901 | Sarilumab for Patients With Moderate COVID-19 Disease: A Randomized Controlled Trial With a Play-The-Winner Design | Sarilumab | Anti-IL-6 Receptor | RCT | 120 | 2 |
NCT04322188 | An Observational Case-control Study of the Use of Siltuximab in ARDS Patients Diagnosed With COVID-19 Infection | Siltuximab | Anti-IL-6 | Case-Control | 50 | N/A |
NCT04343989 | A Randomized Placebo-controlled Safety and Dose-finding Study for the Use of the IL-6 Inhibitor Clazakizumab in Patients with Life-threatening COVID-19 Infection | Clazakizumab | Anti-IL-6 | RCT | 30 | 2 |
NCT04348500 | Clazakizumab (Anti-IL- 6 Monoclonal) Compared to Placebo for COVID19 Disease | Clazakizumab | Anti-IL-6 | RCT | 60 | 2 |
NCT04363502 | Use of the Interleukin-6 Inhibitor Clazakizumab in Patients With Life-threatening COVID-19 Infection | Clazakizumab | Anti-IL-6 | RCT | 30 | 2 |
ChiCTR2000030196 | A multicenter, single arm, open label trial for the efficacy and safety of CMAB806 in the treatment of cytokine release syndrome of novel coronavirus pneumonia (COVID-19) | Conventional therapy+ Tocilizumab | Anti-IL-6R | Single arm | 60 | 2 |
NCT04362813 | Study of Efficacy and Safety of Canakinumab Treatment for CRS in Participants With COVID-19-induced Pneumonia | Canakinumab | Anti-IL-1β | RCT | 450 | 3 |
NCT04365153 | Canakinumab to Reduce Deterioration of Cardiac and Respiratory Function Due to COVID-19 | Canakinumab | Anti-IL-1β | RCT | 45 | 2 |
NCT04362111 | Early Identification and Treatment of Cytokine Storm Syndrome in Covid-19 | Anakinra | Anti-IL-1 Receptor | RCT | 20 | 3 |
NCT04357366 | suPAR-guided Anakinra Treatment for Validation of the Risk and Management of Respiratory Failure by COVID-19 (SAVE) | Anakinra or trimethoprim/sulfamethoxazole | Anti-IL-1 Receptor or Anti-inflammation | Single arm | 100 | 2 |
NCT04364009 | Anakinra for COVID-19 Respiratory Symptoms | Anakinra | Anti-IL-1 Receptor | RCT | 240 | 3 |
NCT04366232 | Efficacy of Intravenous Anakinra and Ruxolitinib During COVID-19 Inflammation (JAKINCOV) | Anakinra+ Ruxolitinib | Anti-IL-1 Receptor+ JAK inhibitor | RCT | 50 | 2 |
NCT04330638 | Treatment of COVID-19 Patients with Anti-interleukin Drugs | Anakinra+ Siltuximab+ Tocilizumab | IL-1 receptor Antagonist+ Anti-IL-6+ Anti-IL-6 Receptor | RCT | 342 | 3 |
ChiCTR2000030089 | A clinical study for the efficacy and safety of Adalimumab Injection in the treatment of patients with severe novel coronavirus pneumonia (COVID-19) | Adalimumab | Anti-TNF-alpha | RCT | 60 | 4 |
ChiCTR2000030580 | Efficacy and safety of adamumab combined with tozumab in severe and critical patients with novel coronavirus pneumonia (COVID-19) | Adalimumab and Tocilizumab | Anti-TNF-alpha Anti-IL-6 Receptor | RCT | 60 | 4 |
NCT04324021 | Efficacy and Safety of Emapalumab and Anakinra in Reducing Hyperinflammation and Respiratory Distress in Patients With COVID-19 Infection. | Emapalumab and Anakinra | Anti-IFN-γ IL-1 receptor Antagonist | RCT | 54 | 3 |
ChiCTR2000030703 | A randomized, blinded, controlled, multicenter clinical trial to evaluate the efficacy and safety of Ixekizumab combined with conventional antiviral drugs in patients with novel coronavirus pneumonia (COVID-19) | Ixekizumab | Anti-IL-17A | RCT | 40 | 0 |
NCT04347226 | Anti-Interleukin-8 (Anti-IL-8) for Cancer Patients With COVID-19 | BMS-986253 | Anti-IL-8 | RCT | 138 | 2 |
NCT04275245 | Clinical Study of Anti-CD147 Humanized Meplazumab for Injection to Treat With 2019-nCoV Pneumonia | Humanized Meplazumab | Anti-CD147 | Single arm | 20 | 2 |
NCT04337216 | Mavrilimumab to Reduce Progression of Acute Respiratory Failure in Patients with Severe COVID-19 Pneumonia and Systemic Hyper-inflammation | Mavrilimumab | Anti-GM-CSF-R | Single arm | 10 | 2 |
NCT04341116 | Study of TJ003234 (Anti-GM-CSF Monoclonal Antibody) in Subjects With Severe Coronavirus Disease 2019 (COVID-19) | Anti-GM-CSF Monoclonal Antibody | Anti-GM-CSF | RCT | 144 | 3 |
NCT04343651 | Study to Evaluate the Efficacy and Safety of Leronlimab for Mild to Moderate COVID-19 | Leronlimab | CCR5 blockading | RCT | 75 | 2 |
NCT04347239 | Study to Evaluate the Efficacy and Safety of Leronlimab for Patients With Severe or Critical Coronavirus Disease 2019 (COVID-19) | Leronlimab | CCR5 blockading | RCT | 390 | 2 |
ChiCTR2000030262 | Clinical study for combination of anti-viral drugs and type I interferon and inflammation inhibitor TFF2 in the treatment of novel coronavirus pneumonia (COVID-19) | type I interferon and TFF2 | Boost innate resistance Anti-inflammatory peptide | RCT | 30 | 0 |
ChiCTR2000029572 | Safety and efficacy of umbilical cord blood mononuclear cells in the treatment of severe and critically 2019-nCoV pneumonia (novel coronavirus pneumonia, NCP): a randomized controlled clinical trial | Umbilical cord blood mononuclear cells | Anti-inflammatory, Anti-fibrotic | RCT | 30 | 0 |
ChiCTR2000029606 | Clinical Study for Human Menstrual Blood-Derived Stem Cells in the Treatment of Acute Novel Coronavirus Pneumonia (NCP) | Human Menstrual Blood-Derived Stem Cells | Anti-inflammatory, Anti-fibrotic | RCT | 63 | 0 |
ChiCTR2000029990 | Clinical trials of mesenchymal stem cells for the treatment of pneumonitis caused by novel coronavirus pneumonia (COVID-19) | Mesenchymal stem cells | Anti-inflammatory, Anti-fibrotic | RCT | 120 | 2 |
ChiCTR2000030116 | Safety and effectiveness of human umbilical cord mesenchymal stem cells in the treatment of acute respiratory distress syndrome of severe novel coronavirus pneumonia (COVID-19) | Human umbilical cord mesenchymal stem cells | Anti-inflammatory, Anti-fibrotic | CCT | 16 | N/A |
ChiCTR2000030866 | Open-label, observational study of human umbilical cord derived mesenchymal stem cells in the treatment of severe and critical patients with novel coronavirus pneumonia (COVID-19) | Human umbilical cord derived mesenchymal stem cells | Anti-inflammatory, Anti-fibrotic | Single arm | 30 | 0 |
NCT04299152 | Stem Cell Educator Therapy Treat the Viral Inflammation Caused by Severe Acute Respiratory Syndrome Coronavirus 2 | Stem Cell | Immune suppression | RCT | 20 | 2 |
NCT04333368 | Cell Therapy Using Umbilical Cord-derived Mesenchymal Stromal Cells in SARS-CoV-2-related ARDS | Umbilical Cord-derived Mesenchymal Stromal Cells | Anti-inflammatory, Anti-fibrotic | RCT | 60 | 2 |
NCT04345601 | Mesenchymal Stromal Cells for the Treatment of SARS-CoV-2 Induced Acute Respiratory Failure (COVID-19 Disease) | Mesenchymal Stromal Cells | Anti-inflammatory, Anti-fibrotic | Single arm | 30 | 1 |
NCT04361942 | Treatment of Severe COVID-19 Pneumonia With Allogeneic Mesenchymal Stromal Cells (COVID_MSV) | Allogeneic Mesenchymal Stromal Cells | Anti-inflammatory, Anti-fibrotic | RCT | 24 | 2 |
NCT04366063 | Mesenchymal Stem Cell Therapy for SARS-CoV-2-related Acute Respiratory Distress Syndrome | Mesenchymal Stem Cell | Anti-inflammatory, Anti-fibrotic | RCT | 60 | 3 |
NCT04366830 | Intermediate-size Expanded Access Program (EAP), Mesenchymal Stromal Cells (MSC) for Acute Respiratory Distress Syndrome (ARDS) Due to COVID-19 Infection | EAP+MSCs | Anti-inflammatory, Anti-fibrotic | N/A | N/A | N/A |
NCT04371393 | MSCs in COVID-19 ARDS | MSCs | Anti-inflammatory, Anti-fibrotic | RCT | 300 | 3 |
ChiCTR2000029898 | A Randomized, Open-label, Parallel, Controlled Trial for Evaluation of the Efficacy and Safety of Chloroquine Phosphate in the treatment of Severe Patients with Novel Coronavirus Pneumonia (COVID-19) | Chloroquine Phosphate | Immune suppression | RCT | 100 | 4 |
NCT04323631 | Hydroxychloroquine for the Treatment of Patients with Mild to Moderate COVID-19 to Prevent Progression to Severe Infection or Death | Hydroxychloroquine | Immune suppression | RCT | 1116 | 1 |
NCT04323527 | Chloroquine Diphosphate for the Treatment of Severe Acute Respiratory Syndrome Secondary to SARS-CoV2 | Chloroquine Diphosphate | Immune suppression | RCT | 440 | 2 |
NCT04358068 | Evaluating the Efficacy of Hydroxychloroquine and Azithromycin to Prevent Hospitalization or Death in Persons With COVID-19 | Hydroxychloroquine +Azithromycin | Anti-inflammation | RCT | 2000 | 2 |
NCT04358081 | Hydroxychloroquine Monotherapy and in Combination With Azithromycin in Patients With Moderate and Severe COVID-19 Disease | Hydroxychloroquine+ Monotherapy+ Azithromycin | Anti-inflammation | RCT | 444 | 3 |
NCT04362332 | Chloroquine, Hydroxychloroquine or Only Supportive Care in Patients AdmItted With Moderate to Severe COVID-19 | Chloroquine+ Hydroxychloroquine | Anti-inflammation | RCT | 950 | 4 |
ChiCTR2000029757 | Convalescent plasma for the treatment of severe novel coronavirus pneumonia (COVID-19): a prospective randomized controlled trial | Convalescent plasma | Convalescent plasma | RCT | 200 | 0 |
ChiCTR2000029850 | Study for convalescent plasma treatment for severe patients with novel coronavirus pneumonia (COVID-19) | Convalescent plasma | Convalescent plasma | CCT | 20 | 0 |
ChiCTR2000030010 | A randomized, double-blind, parallel-controlled, trial to evaluate the efficacy and safety of anti-SARS-CoV-2 virus inactivated plasma in the treatment of severe novel coronavirus pneumonia patients (COVID-19) | Anti-SARS-CoV-2 virus inactivated plasma | Convalescent plasma | RCT | 100 | N/A |
ChiCTR2000030929 | A randomized, double-blind, parallel-controlled trial to evaluate the efficacy and safety of anti-SARS-CoV-2 virus inactivated plasma in the treatment of severe novel coronavirus pneumonia (COVID-19) | Anti-SARS-CoV-2 virus inactivated plasma | Convalescent plasma | RCT | 60 | N/A |
NCT04346446 | Efficacy of Convalescent Plasma Therapy in Severely Sick COVID-19 Patients | Convalescent Plasma in severe COVID-19 Patients | Convalescent Plasma | RCT | 20 | 2 |
NCT04347681 | Potential Efficacy of Convalescent Plasma to Treat Severe COVID-19 and Patients at High Risk of Developing Severe COVID-19 | Convalescent Plasma | Convalescent Plasma | CCT | 40 | 2 |
NCT04353206 | Convalescent Plasma in ICU Patients With COVID-19-induced Respiratory Failure | Convalescent Plasma in ICU Patients | Convalescent plasma | Single arm | 90 | 1 |
NCT04359810 | Plasma Therapy of COVID-19 in Critically Ill Patients | Convalescent Plasma | Convalescent plasma | RCT | 105 | 2 |
ChiCTR2000030475 | Cytosorb in Treating Critically Ill Hospitalized Adult Patients with novel coronavirus pneumonia (COVID-19) | Cytosorb | Broad Cytokine/Toxin Removal | Single arm | 19 | 0 |
NCT04324528 | Cytokine Adsorption in Severe COVID-19 Pneumonia Requiring Extracorporeal Membrane Oxygenation | Cytokine Adsorption+ Extracorporeal Membrane Oxygenation | Broad Cytokine/Toxin Removal | Case reports | 30 | R/A |
NCT04344080 | Effect of CytoSorb Adsorber on Hemodynamic and Immunological Parameters in Critical Ill Patients With COVID-19 | CytoSorb | Broad Cytokine/Toxin Removal | RCT | 24 | N/A |
NCT04358003 | Plasma Adsorption in Patients With Confirmed COVID-19 | Plasma Adsorption | Broad Cytokine/Toxin Removal | Single arm | 2000 | N/A |
NCT04374149 | Therapeutic Plasma Exchange Alone or in Combination With Ruxolitinib in COVID-19 Associated CRS | Plasma Exchange | Broad Cytokine/Toxin Removal | CCT | 20 | 2 |
NCT04374539 | Plasma Exchange in Patients With COVID-19 Disease and Invasive Mechanical Ventilation: a Randomized Controlled Trial | Plasma Exchange | Broad Cytokine/Toxin Removal | RCT | 116 | 2 |
NCT04273581 | The Efficacy and Safety of Thalidomide Combined with Low-dose Hormones in the Treatment of Severe COVID-19 | Thalidomide and Interferon-alpha | Prevent lung injury Boost Innate resistance | RCT | 40 | 2 |
NCT04293887 | Efficacy and Safety of IFN-α2β in the Treatment of Novel Coronavirus Patients | IFN-α2β | Boost Innate Resistance | RCT | 328 | 1 |
NCT04343768 | An Investigation into Beneficial Effects of Interferon Beta 1a, Compared to Interferon Beta 1b And The Base Therapeutic Regiment in Moderate to Severe COVID-19: A Randomized Clinical Trial | Interferon Beta 1a or Interferon Beta 1b | Boost Innate Resistance | RCT | 60 | 4 |
NCT04325061 | Efficacy of Dexamethasone Treatment for Patients with ARDS Caused by COVID-19 | Dexamethasone | Anti-inflammatory | RCT | 200 | 4 |
NCT04347980 | Dexamethasone Treatment for Severe Acute Respiratory Distress Syndrome Induced by COVID-19 | Dexamethasone | Anti-inflammatory | RCT | 122 | 3 |
NCT04327401 | COVID-19-associated ARDS Treated with Dexamethasone: Alliance Covid-19 Brasil III | Dexamethasone | Immune Suppression | RCT | 290 | 3 |
NCT04358627 | Dexmedetomidine to Improve Outcomes of ARDS in Critical Care COVID-19 Patients | Dexmedetomidine | Immune Suppression | Case | 80 | N/A |
NCT04355247 | Prophylactic Corticosteroid to Prevent COVID-19 Cytokine Storm | Corticosteroid | Immune Suppression | Single arm | 20 | 2 |
NCT04360876 | Targeted Steroids for ARDS Due to COVID-19 Pneumonia: A Pilot Randomized Clinical Trial | Steroids | Immune Suppression | RCT | 90 | 2 |
NCT04323592 | Efficacy of Methylprednisolone for Patients With COVID-19 Severe Acute Respiratory Syndrome | Methylprednisolone | Anti-inflammatory | CCT | 104 | 3 |
NCT04343729 | Methylprednisolone in the Treatment of Patients with Signs of Severe Acute Respiratory Syndrome in Covid-19 | Methylprednisolone | Anti-inflammatory | RCT | 420 | 2 |
NCT04306393 | Nitric Oxide Gas Inhalation in Severe Acute Respiratory Syndrome in COVID-19 | Nitric Oxide Gas | Pulmonary vasodilator | RCT | 200 | 2 |
NCT04358588 | Pulsed Inhaled Nitric Oxide for the Treatment of Patients With Mild or Moderate COVID-19 | Nitric Oxide | Anti-inflammation | N/A | N/A | N/A |
NCT04244591 | Glucocorticoid Therapy for Novel Coronavirus Critically Ill Patients With Severe Acute Respiratory Failure | Glucocorticoid | Immune suppression | RCT | 80 | 3 |
NCT04320277 | Baricitinib in Symptomatic Patients Infected by COVID-19: an Open-label, Pilot Study. | Baricitinib | JAK inhibitor | CCT | 60 | 3 |
NCT04340232 | Safety and Efficacy of Baricitinib for COVID-19 | Baricitinib | JAK inhibitor | Single arm | 80 | 3 |
NCT04359290 | Ruxolitinib for Treatment of Covid-19 Induced Lung Injury ARDS | Ruxolitinib | JAK inhibitor | Single arm | 15 | 2 |
NCT04355793 | Expanded Access Program of Ruxolitinib for the Emergency Treatment of Cytokine Storm From COVID-19 Infection | Ruxolitinib | JAK inhibitor | N/A | N/A | N/A |
NCT04361903 | Ruxolitinib for the Treatment of Acute Respiratory Distress Syndrome in Patients With COVID-19 Infection | Ruxolitinib | JAK inhibitor | Cohort | 13 | N/A |
NCT04362137 | Phase 3 Randomized, Double-blind, Placebo-controlled Multi-center Study to Assess the Efficacy and Safety of Ruxolitinib in Patients With COVID-19 Associated Cytokine Storm (RUXCOVID) | Ruxolitinib | JAK inhibitor | RCT | 402 | 3 |
NCT04321993 | Treatment of Moderate to Severe Coronavirus Disease (COVID-19) in Hospitalized Patients | Baricitinib+ Sarilumab+Lopinavir/ritonavir+Hydroxychloroquine sulfate | JAK inhibitor+ Anti-IL-6+ Anti-virus+ Anti-inflammatory | CCT | 1000 | 2 |
NCT04373044 | Antiviral Therapy and Baricitinib for the Treatment of Patients With Moderate or Severe COVID-19 | Antiviral Therapy+Baricitinib | Anti-virus+JAK inhibitor | Single arm | 59 | 2 |
NCT04348383 | Defibrotide as Prevention and Treatment of Respiratory Distress and Cytokine Release Syndrome of Covid 19. | Defibrotide | Anti-inflammatory | RCT | 120 | 2 |
NCT04357444 | Low Dose of IL-2 In Acute Respiratory DistrEss Syndrome Related to COVID-19 | IL-2 | Anti-inflammation | RCT | 30 | 2 |
NCT04355364 | Efficacy and Safety of Aerosolized Intra-tracheal Dornase Alpha Administration in Patients With COVID19-induced ARDS (COVIDORNASE) | Aerosolized Intra-tracheal Dornase Alpha | Anti-inflammation | RCT | 100 | 3 |
NCT04363437 | COlchicine in Moderate Severity Hospitalized Patients Before ARDS to Treat COVID-19 | Colchicine | Anti-inflammation | RCT | 70 | 2 |
NCT04366791 | Radiation Eliminates Storming Cytokines and Unchecked Edema as a 1-Day Treatment for COVID-19 | Radiation | Other | Single arm | 10 | 2 |
Register Number . | Title . | Drugs/Strategies . | Therapeutic Target . | Study design . | Samples . | Phase . |
---|---|---|---|---|---|---|
ChiCTR2000029765 | A multicenter, randomized controlled trial for the efficacy and safety of tocilizumab in the treatment of new coronavirus pneumonia (COVID-19) | Tocilizumab | Anti-IL-6 Receptor | RCT | 188 | 4 |
ChiCTR2000030196 | A multicenter, single arm, open label trial for the efficacy and safety of CMAB806 in the treatment of cytokine release syndrome of novel coronavirus pneumonia (COVID-19) | Tocilizumab | Anti-IL-6 Receptor | Single arm | 60 | 2 |
NCT04317092 | Tocilizumab in COVID-19 Pneumonia (TOCIVID-19) | Tocilizumab | Anti-IL-6 Receptor | Single arm | 330 | 2 |
NCT04320615 | A Study to Evaluate the Safety and Efficacy of Tocilizumab in Patients with Severe COVID-19 Pneumonia | Tocilizumab | Anti-IL-6 Receptor | RCT | 330 | 3 |
NCT04310228 | Favipiravir Combined with Tocilizumab in the Treatment of Corona Virus Disease 2019 | Tocilizumab | Anti-IL-6 Receptor | RCT | 150 | N/A |
NCT04306705 | Tocilizumab vs CRRT in Management of Cytokine Release Syndrome (CRS) in COVID-19 | Tocilizumab | Anti-IL-6 Receptor | Cohort study | 120 | N/A |
NCT04315480 | Tocilizumab for SARS-CoV2 Severe Pneumonitis | Tocilizumab | Anti-IL-6 Receptor | Single arm | 30 | 2 |
NCT04331795 | Tocilizumab to Prevent Clinical Decompensation in Hospitalized, Non-critically Ill Patients With COVID-19 Pneumonitis | Tocilizumab | Anti-IL-6 Receptor | RCT | 50 | 2 |
NCT04331808 | CORIMUNO-19 - Tocilizumab Trial - TOCI (CORIMUNO-TOCI) | Tocilizumab | Anti-IL-6 Receptor | RCT | 240 | 2 |
NCT04332913 | Efficacy and Safety of Tocilizumab in the Treatment of SARS-Cov-2 Related Pneumonia | Tocilizumab | Anti-IL-6 Receptor | Cohort study | 30 | N/A |
NCT04335071 | Tocilizumab in the Treatment of Coronavirus Induced Disease (COVID-19) | Tocilizumab | Anti-IL-6 Receptor | RCT | 100 | 2 |
NCT04346355 | Efficacy of Early Administration of Tocilizumab in COVID-19 Patients | Tocilizumab | Anti-IL-6 Receptor | RCT | 398 | 2 |
NCT04356937 | Efficacy of Tocilizumab on Patients With COVID-19 | Tocilizumab | Anti-IL-6 Receptor | RCT | 300 | 3 |
NCT04359667 | Serum IL-6 and Soluble IL-6 Receptor in Severe COVID-19 Pneumonia Treated With Tocilizumab | Tocilizumab | Anti-IL-6 Receptor | Case | 30 | N/A |
NCT04361032 | Assessment of Efficacy and Safety of Tocilizumab Compared to Deferoxamine, Associated With Standards Treatments in COVID-19 (+) Patients Hospitalized In Intensive Care in Tunisia | Tocilizumab/Deferoxamine | Anti-IL-6 Receptor | RCT | 260 | 3 |
NCT04361552 | Tocilizumab for the Treatment of Cytokine Release Syndrome in Patients With COVID-19 (SARS-CoV-2 Infection) | Tocilizumab | Anti-IL-6 Receptor | RCT | 180 | 3 |
NCT04363736 | A Study to Investigate Intravenous Tocilizumab in Participants With Moderate to Severe COVID-19 Pneumonia | Tocilizumab | Anti-IL-6 Receptor | RCT | 100 | 2 |
NCT04363853 | Tocilizumab Treatment in Patients With COVID-19 | Tocilizumab | Anti-IL-6 Receptor | Single arm | 200 | 2 |
NCT04370834 | Tocilizumab for Patients With Cancer and COVID-19 Disease | Tocilizumab | Anti-IL-6 Receptor | Single arm | 200 | 2 |
NCT04372186 | A Study to Evaluate the Efficacy and Safety of Tocilizumab in Hospitalized Participants With COVID-19 Pneumonia | Tocilizumab | Anti-IL-6 Receptor | RCT | 379 | 3 |
NCT04322773 | Anti-il6 Treatment of Serious COVID-19 Disease with Threatening Respiratory Failure | Tocilizumab + Sarilumab | Anti-IL-6 Receptor | RCT | 200 | 2 |
NCT04345445 | Study to Evaluate the Efficacy and Safety of Tocilizumab Versus Corticosteroids in Hospitalised COVID-19 Patients with High Risk of Progression | Tocilizumab or Corticosteroids | Anti-IL-6 Receptor Glucocorticoid | RCT | 310 | 3 |
NCT04315298 | Evaluation of the Efficacy and Safety of Sarilumab in Hospitalized Patients With COVID-19 | Sarilumab | Anti-IL-6 Receptor | RCT | 400 | 3 |
NCT04324073 | Cohort Multiple Randomized Controlled Trials Open-label of Immune Modulatory Drugs and Other Treatments in COVID-19 Patients - Sarilumab Trial - CORIMUNO-19 - SARI | Sarilumab | Anti-IL-6 Receptor | RCT | 240 | 3 |
NCT04357808 | Efficacy of Subcutaneous Sarilumab in Hospitalised Patients With Moderate-severe COVID-19 Infection (SARCOVID) | Sarilumab | Anti-IL-6 Receptor | RCT | 30 | 2 |
NCT04357860 | Clinical Trial of Sarilumab in Adults With COVID-19 | Sarilumab | Anti-IL-6 Receptor | RCT | 120 | 2 |
NCT04359901 | Sarilumab for Patients With Moderate COVID-19 Disease: A Randomized Controlled Trial With a Play-The-Winner Design | Sarilumab | Anti-IL-6 Receptor | RCT | 120 | 2 |
NCT04322188 | An Observational Case-control Study of the Use of Siltuximab in ARDS Patients Diagnosed With COVID-19 Infection | Siltuximab | Anti-IL-6 | Case-Control | 50 | N/A |
NCT04343989 | A Randomized Placebo-controlled Safety and Dose-finding Study for the Use of the IL-6 Inhibitor Clazakizumab in Patients with Life-threatening COVID-19 Infection | Clazakizumab | Anti-IL-6 | RCT | 30 | 2 |
NCT04348500 | Clazakizumab (Anti-IL- 6 Monoclonal) Compared to Placebo for COVID19 Disease | Clazakizumab | Anti-IL-6 | RCT | 60 | 2 |
NCT04363502 | Use of the Interleukin-6 Inhibitor Clazakizumab in Patients With Life-threatening COVID-19 Infection | Clazakizumab | Anti-IL-6 | RCT | 30 | 2 |
ChiCTR2000030196 | A multicenter, single arm, open label trial for the efficacy and safety of CMAB806 in the treatment of cytokine release syndrome of novel coronavirus pneumonia (COVID-19) | Conventional therapy+ Tocilizumab | Anti-IL-6R | Single arm | 60 | 2 |
NCT04362813 | Study of Efficacy and Safety of Canakinumab Treatment for CRS in Participants With COVID-19-induced Pneumonia | Canakinumab | Anti-IL-1β | RCT | 450 | 3 |
NCT04365153 | Canakinumab to Reduce Deterioration of Cardiac and Respiratory Function Due to COVID-19 | Canakinumab | Anti-IL-1β | RCT | 45 | 2 |
NCT04362111 | Early Identification and Treatment of Cytokine Storm Syndrome in Covid-19 | Anakinra | Anti-IL-1 Receptor | RCT | 20 | 3 |
NCT04357366 | suPAR-guided Anakinra Treatment for Validation of the Risk and Management of Respiratory Failure by COVID-19 (SAVE) | Anakinra or trimethoprim/sulfamethoxazole | Anti-IL-1 Receptor or Anti-inflammation | Single arm | 100 | 2 |
NCT04364009 | Anakinra for COVID-19 Respiratory Symptoms | Anakinra | Anti-IL-1 Receptor | RCT | 240 | 3 |
NCT04366232 | Efficacy of Intravenous Anakinra and Ruxolitinib During COVID-19 Inflammation (JAKINCOV) | Anakinra+ Ruxolitinib | Anti-IL-1 Receptor+ JAK inhibitor | RCT | 50 | 2 |
NCT04330638 | Treatment of COVID-19 Patients with Anti-interleukin Drugs | Anakinra+ Siltuximab+ Tocilizumab | IL-1 receptor Antagonist+ Anti-IL-6+ Anti-IL-6 Receptor | RCT | 342 | 3 |
ChiCTR2000030089 | A clinical study for the efficacy and safety of Adalimumab Injection in the treatment of patients with severe novel coronavirus pneumonia (COVID-19) | Adalimumab | Anti-TNF-alpha | RCT | 60 | 4 |
ChiCTR2000030580 | Efficacy and safety of adamumab combined with tozumab in severe and critical patients with novel coronavirus pneumonia (COVID-19) | Adalimumab and Tocilizumab | Anti-TNF-alpha Anti-IL-6 Receptor | RCT | 60 | 4 |
NCT04324021 | Efficacy and Safety of Emapalumab and Anakinra in Reducing Hyperinflammation and Respiratory Distress in Patients With COVID-19 Infection. | Emapalumab and Anakinra | Anti-IFN-γ IL-1 receptor Antagonist | RCT | 54 | 3 |
ChiCTR2000030703 | A randomized, blinded, controlled, multicenter clinical trial to evaluate the efficacy and safety of Ixekizumab combined with conventional antiviral drugs in patients with novel coronavirus pneumonia (COVID-19) | Ixekizumab | Anti-IL-17A | RCT | 40 | 0 |
NCT04347226 | Anti-Interleukin-8 (Anti-IL-8) for Cancer Patients With COVID-19 | BMS-986253 | Anti-IL-8 | RCT | 138 | 2 |
NCT04275245 | Clinical Study of Anti-CD147 Humanized Meplazumab for Injection to Treat With 2019-nCoV Pneumonia | Humanized Meplazumab | Anti-CD147 | Single arm | 20 | 2 |
NCT04337216 | Mavrilimumab to Reduce Progression of Acute Respiratory Failure in Patients with Severe COVID-19 Pneumonia and Systemic Hyper-inflammation | Mavrilimumab | Anti-GM-CSF-R | Single arm | 10 | 2 |
NCT04341116 | Study of TJ003234 (Anti-GM-CSF Monoclonal Antibody) in Subjects With Severe Coronavirus Disease 2019 (COVID-19) | Anti-GM-CSF Monoclonal Antibody | Anti-GM-CSF | RCT | 144 | 3 |
NCT04343651 | Study to Evaluate the Efficacy and Safety of Leronlimab for Mild to Moderate COVID-19 | Leronlimab | CCR5 blockading | RCT | 75 | 2 |
NCT04347239 | Study to Evaluate the Efficacy and Safety of Leronlimab for Patients With Severe or Critical Coronavirus Disease 2019 (COVID-19) | Leronlimab | CCR5 blockading | RCT | 390 | 2 |
ChiCTR2000030262 | Clinical study for combination of anti-viral drugs and type I interferon and inflammation inhibitor TFF2 in the treatment of novel coronavirus pneumonia (COVID-19) | type I interferon and TFF2 | Boost innate resistance Anti-inflammatory peptide | RCT | 30 | 0 |
ChiCTR2000029572 | Safety and efficacy of umbilical cord blood mononuclear cells in the treatment of severe and critically 2019-nCoV pneumonia (novel coronavirus pneumonia, NCP): a randomized controlled clinical trial | Umbilical cord blood mononuclear cells | Anti-inflammatory, Anti-fibrotic | RCT | 30 | 0 |
ChiCTR2000029606 | Clinical Study for Human Menstrual Blood-Derived Stem Cells in the Treatment of Acute Novel Coronavirus Pneumonia (NCP) | Human Menstrual Blood-Derived Stem Cells | Anti-inflammatory, Anti-fibrotic | RCT | 63 | 0 |
ChiCTR2000029990 | Clinical trials of mesenchymal stem cells for the treatment of pneumonitis caused by novel coronavirus pneumonia (COVID-19) | Mesenchymal stem cells | Anti-inflammatory, Anti-fibrotic | RCT | 120 | 2 |
ChiCTR2000030116 | Safety and effectiveness of human umbilical cord mesenchymal stem cells in the treatment of acute respiratory distress syndrome of severe novel coronavirus pneumonia (COVID-19) | Human umbilical cord mesenchymal stem cells | Anti-inflammatory, Anti-fibrotic | CCT | 16 | N/A |
ChiCTR2000030866 | Open-label, observational study of human umbilical cord derived mesenchymal stem cells in the treatment of severe and critical patients with novel coronavirus pneumonia (COVID-19) | Human umbilical cord derived mesenchymal stem cells | Anti-inflammatory, Anti-fibrotic | Single arm | 30 | 0 |
NCT04299152 | Stem Cell Educator Therapy Treat the Viral Inflammation Caused by Severe Acute Respiratory Syndrome Coronavirus 2 | Stem Cell | Immune suppression | RCT | 20 | 2 |
NCT04333368 | Cell Therapy Using Umbilical Cord-derived Mesenchymal Stromal Cells in SARS-CoV-2-related ARDS | Umbilical Cord-derived Mesenchymal Stromal Cells | Anti-inflammatory, Anti-fibrotic | RCT | 60 | 2 |
NCT04345601 | Mesenchymal Stromal Cells for the Treatment of SARS-CoV-2 Induced Acute Respiratory Failure (COVID-19 Disease) | Mesenchymal Stromal Cells | Anti-inflammatory, Anti-fibrotic | Single arm | 30 | 1 |
NCT04361942 | Treatment of Severe COVID-19 Pneumonia With Allogeneic Mesenchymal Stromal Cells (COVID_MSV) | Allogeneic Mesenchymal Stromal Cells | Anti-inflammatory, Anti-fibrotic | RCT | 24 | 2 |
NCT04366063 | Mesenchymal Stem Cell Therapy for SARS-CoV-2-related Acute Respiratory Distress Syndrome | Mesenchymal Stem Cell | Anti-inflammatory, Anti-fibrotic | RCT | 60 | 3 |
NCT04366830 | Intermediate-size Expanded Access Program (EAP), Mesenchymal Stromal Cells (MSC) for Acute Respiratory Distress Syndrome (ARDS) Due to COVID-19 Infection | EAP+MSCs | Anti-inflammatory, Anti-fibrotic | N/A | N/A | N/A |
NCT04371393 | MSCs in COVID-19 ARDS | MSCs | Anti-inflammatory, Anti-fibrotic | RCT | 300 | 3 |
ChiCTR2000029898 | A Randomized, Open-label, Parallel, Controlled Trial for Evaluation of the Efficacy and Safety of Chloroquine Phosphate in the treatment of Severe Patients with Novel Coronavirus Pneumonia (COVID-19) | Chloroquine Phosphate | Immune suppression | RCT | 100 | 4 |
NCT04323631 | Hydroxychloroquine for the Treatment of Patients with Mild to Moderate COVID-19 to Prevent Progression to Severe Infection or Death | Hydroxychloroquine | Immune suppression | RCT | 1116 | 1 |
NCT04323527 | Chloroquine Diphosphate for the Treatment of Severe Acute Respiratory Syndrome Secondary to SARS-CoV2 | Chloroquine Diphosphate | Immune suppression | RCT | 440 | 2 |
NCT04358068 | Evaluating the Efficacy of Hydroxychloroquine and Azithromycin to Prevent Hospitalization or Death in Persons With COVID-19 | Hydroxychloroquine +Azithromycin | Anti-inflammation | RCT | 2000 | 2 |
NCT04358081 | Hydroxychloroquine Monotherapy and in Combination With Azithromycin in Patients With Moderate and Severe COVID-19 Disease | Hydroxychloroquine+ Monotherapy+ Azithromycin | Anti-inflammation | RCT | 444 | 3 |
NCT04362332 | Chloroquine, Hydroxychloroquine or Only Supportive Care in Patients AdmItted With Moderate to Severe COVID-19 | Chloroquine+ Hydroxychloroquine | Anti-inflammation | RCT | 950 | 4 |
ChiCTR2000029757 | Convalescent plasma for the treatment of severe novel coronavirus pneumonia (COVID-19): a prospective randomized controlled trial | Convalescent plasma | Convalescent plasma | RCT | 200 | 0 |
ChiCTR2000029850 | Study for convalescent plasma treatment for severe patients with novel coronavirus pneumonia (COVID-19) | Convalescent plasma | Convalescent plasma | CCT | 20 | 0 |
ChiCTR2000030010 | A randomized, double-blind, parallel-controlled, trial to evaluate the efficacy and safety of anti-SARS-CoV-2 virus inactivated plasma in the treatment of severe novel coronavirus pneumonia patients (COVID-19) | Anti-SARS-CoV-2 virus inactivated plasma | Convalescent plasma | RCT | 100 | N/A |
ChiCTR2000030929 | A randomized, double-blind, parallel-controlled trial to evaluate the efficacy and safety of anti-SARS-CoV-2 virus inactivated plasma in the treatment of severe novel coronavirus pneumonia (COVID-19) | Anti-SARS-CoV-2 virus inactivated plasma | Convalescent plasma | RCT | 60 | N/A |
NCT04346446 | Efficacy of Convalescent Plasma Therapy in Severely Sick COVID-19 Patients | Convalescent Plasma in severe COVID-19 Patients | Convalescent Plasma | RCT | 20 | 2 |
NCT04347681 | Potential Efficacy of Convalescent Plasma to Treat Severe COVID-19 and Patients at High Risk of Developing Severe COVID-19 | Convalescent Plasma | Convalescent Plasma | CCT | 40 | 2 |
NCT04353206 | Convalescent Plasma in ICU Patients With COVID-19-induced Respiratory Failure | Convalescent Plasma in ICU Patients | Convalescent plasma | Single arm | 90 | 1 |
NCT04359810 | Plasma Therapy of COVID-19 in Critically Ill Patients | Convalescent Plasma | Convalescent plasma | RCT | 105 | 2 |
ChiCTR2000030475 | Cytosorb in Treating Critically Ill Hospitalized Adult Patients with novel coronavirus pneumonia (COVID-19) | Cytosorb | Broad Cytokine/Toxin Removal | Single arm | 19 | 0 |
NCT04324528 | Cytokine Adsorption in Severe COVID-19 Pneumonia Requiring Extracorporeal Membrane Oxygenation | Cytokine Adsorption+ Extracorporeal Membrane Oxygenation | Broad Cytokine/Toxin Removal | Case reports | 30 | R/A |
NCT04344080 | Effect of CytoSorb Adsorber on Hemodynamic and Immunological Parameters in Critical Ill Patients With COVID-19 | CytoSorb | Broad Cytokine/Toxin Removal | RCT | 24 | N/A |
NCT04358003 | Plasma Adsorption in Patients With Confirmed COVID-19 | Plasma Adsorption | Broad Cytokine/Toxin Removal | Single arm | 2000 | N/A |
NCT04374149 | Therapeutic Plasma Exchange Alone or in Combination With Ruxolitinib in COVID-19 Associated CRS | Plasma Exchange | Broad Cytokine/Toxin Removal | CCT | 20 | 2 |
NCT04374539 | Plasma Exchange in Patients With COVID-19 Disease and Invasive Mechanical Ventilation: a Randomized Controlled Trial | Plasma Exchange | Broad Cytokine/Toxin Removal | RCT | 116 | 2 |
NCT04273581 | The Efficacy and Safety of Thalidomide Combined with Low-dose Hormones in the Treatment of Severe COVID-19 | Thalidomide and Interferon-alpha | Prevent lung injury Boost Innate resistance | RCT | 40 | 2 |
NCT04293887 | Efficacy and Safety of IFN-α2β in the Treatment of Novel Coronavirus Patients | IFN-α2β | Boost Innate Resistance | RCT | 328 | 1 |
NCT04343768 | An Investigation into Beneficial Effects of Interferon Beta 1a, Compared to Interferon Beta 1b And The Base Therapeutic Regiment in Moderate to Severe COVID-19: A Randomized Clinical Trial | Interferon Beta 1a or Interferon Beta 1b | Boost Innate Resistance | RCT | 60 | 4 |
NCT04325061 | Efficacy of Dexamethasone Treatment for Patients with ARDS Caused by COVID-19 | Dexamethasone | Anti-inflammatory | RCT | 200 | 4 |
NCT04347980 | Dexamethasone Treatment for Severe Acute Respiratory Distress Syndrome Induced by COVID-19 | Dexamethasone | Anti-inflammatory | RCT | 122 | 3 |
NCT04327401 | COVID-19-associated ARDS Treated with Dexamethasone: Alliance Covid-19 Brasil III | Dexamethasone | Immune Suppression | RCT | 290 | 3 |
NCT04358627 | Dexmedetomidine to Improve Outcomes of ARDS in Critical Care COVID-19 Patients | Dexmedetomidine | Immune Suppression | Case | 80 | N/A |
NCT04355247 | Prophylactic Corticosteroid to Prevent COVID-19 Cytokine Storm | Corticosteroid | Immune Suppression | Single arm | 20 | 2 |
NCT04360876 | Targeted Steroids for ARDS Due to COVID-19 Pneumonia: A Pilot Randomized Clinical Trial | Steroids | Immune Suppression | RCT | 90 | 2 |
NCT04323592 | Efficacy of Methylprednisolone for Patients With COVID-19 Severe Acute Respiratory Syndrome | Methylprednisolone | Anti-inflammatory | CCT | 104 | 3 |
NCT04343729 | Methylprednisolone in the Treatment of Patients with Signs of Severe Acute Respiratory Syndrome in Covid-19 | Methylprednisolone | Anti-inflammatory | RCT | 420 | 2 |
NCT04306393 | Nitric Oxide Gas Inhalation in Severe Acute Respiratory Syndrome in COVID-19 | Nitric Oxide Gas | Pulmonary vasodilator | RCT | 200 | 2 |
NCT04358588 | Pulsed Inhaled Nitric Oxide for the Treatment of Patients With Mild or Moderate COVID-19 | Nitric Oxide | Anti-inflammation | N/A | N/A | N/A |
NCT04244591 | Glucocorticoid Therapy for Novel Coronavirus Critically Ill Patients With Severe Acute Respiratory Failure | Glucocorticoid | Immune suppression | RCT | 80 | 3 |
NCT04320277 | Baricitinib in Symptomatic Patients Infected by COVID-19: an Open-label, Pilot Study. | Baricitinib | JAK inhibitor | CCT | 60 | 3 |
NCT04340232 | Safety and Efficacy of Baricitinib for COVID-19 | Baricitinib | JAK inhibitor | Single arm | 80 | 3 |
NCT04359290 | Ruxolitinib for Treatment of Covid-19 Induced Lung Injury ARDS | Ruxolitinib | JAK inhibitor | Single arm | 15 | 2 |
NCT04355793 | Expanded Access Program of Ruxolitinib for the Emergency Treatment of Cytokine Storm From COVID-19 Infection | Ruxolitinib | JAK inhibitor | N/A | N/A | N/A |
NCT04361903 | Ruxolitinib for the Treatment of Acute Respiratory Distress Syndrome in Patients With COVID-19 Infection | Ruxolitinib | JAK inhibitor | Cohort | 13 | N/A |
NCT04362137 | Phase 3 Randomized, Double-blind, Placebo-controlled Multi-center Study to Assess the Efficacy and Safety of Ruxolitinib in Patients With COVID-19 Associated Cytokine Storm (RUXCOVID) | Ruxolitinib | JAK inhibitor | RCT | 402 | 3 |
NCT04321993 | Treatment of Moderate to Severe Coronavirus Disease (COVID-19) in Hospitalized Patients | Baricitinib+ Sarilumab+Lopinavir/ritonavir+Hydroxychloroquine sulfate | JAK inhibitor+ Anti-IL-6+ Anti-virus+ Anti-inflammatory | CCT | 1000 | 2 |
NCT04373044 | Antiviral Therapy and Baricitinib for the Treatment of Patients With Moderate or Severe COVID-19 | Antiviral Therapy+Baricitinib | Anti-virus+JAK inhibitor | Single arm | 59 | 2 |
NCT04348383 | Defibrotide as Prevention and Treatment of Respiratory Distress and Cytokine Release Syndrome of Covid 19. | Defibrotide | Anti-inflammatory | RCT | 120 | 2 |
NCT04357444 | Low Dose of IL-2 In Acute Respiratory DistrEss Syndrome Related to COVID-19 | IL-2 | Anti-inflammation | RCT | 30 | 2 |
NCT04355364 | Efficacy and Safety of Aerosolized Intra-tracheal Dornase Alpha Administration in Patients With COVID19-induced ARDS (COVIDORNASE) | Aerosolized Intra-tracheal Dornase Alpha | Anti-inflammation | RCT | 100 | 3 |
NCT04363437 | COlchicine in Moderate Severity Hospitalized Patients Before ARDS to Treat COVID-19 | Colchicine | Anti-inflammation | RCT | 70 | 2 |
NCT04366791 | Radiation Eliminates Storming Cytokines and Unchecked Edema as a 1-Day Treatment for COVID-19 | Radiation | Other | Single arm | 10 | 2 |
Abbrevation: ChiCTR, Chinese Clinical Trials Register; NCT, National Clinical Trails; RCT: Random clinical trial; CCT: Controlled clinical trial;
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