03/02/2021

Date Journal Title Study type Country Authors Link Trial identifier Intervention Main question

ESCAPE: An Open‐Label Trial of https://www.medrxiv.or To investigate the outcome of RCT phase anakinra 26‐Jan‐21 BMJ Personalized Immunotherapy in Critically Greece Karakike E, et al. g/content/10.1101/2021 NCT04339712 personalized immunotherapy II tocilizumab Ill COVID‐19 Patients .01.20.21250182v1 in critical COVID‐19.

The effect of early treatment with To evaluate the efficacy of a https://www.thelancet.c ivermectin on viral load, symptoms and single dose of ivermectin om/journals/eclinm/arti EClinical humoral response in patients with non‐ reduce the transmission of 26‐Jan‐21 RCT Spain Chaccour C. et al cle/PIIS2589‐ NCT04390022 Ivermectin Medicine severe COVID‐19: A pilot, double‐blind, SARS‐CoV‐2 when 5370(20)30464‐ placebo‐controlled, randomized clinical administered early after 8/fulltext#%20 trial disease onset.

To determine whether https://www.thelancet.c Effect of anakinra versus usual care in adults anakinra could improve The Lancet om/journals/lanres/artic in hospital with COVID‐19 and mild‐to‐ Internation The CORIMUNO‐19 anakinra outcomes in patients in 22‐Jan‐21 Respiratory RCT le/PIIS2213‐ NCT04341584 moderate pneumonia (CORIMUNO‐ANA‐1): a al Collaborative group tocilizumab hospital with mild‐to‐ medicine 2600(20)30556‐ randomised controlled trial moderate COVID‐19 7/fulltext pneumonia.

To determine the effect of Effect of Bamlanivimab as Monotherapy bamlanivimab monotherapy https://jamanetwork.co bamlanivimab/bamla or in Combination With Etesevimab on and combination therapy with 21‐Jan‐21 JAMA RCT USA Gottlieb R.L., et m/journals/jama/fullarti NCT04427501 nivimab and Viral Load in Patients With Mild to bamlanivimab and etesevimab cle/2775647 etesevimab Moderate COVID‐19 (BLAZE‐1 study) on SARSCoV‐2 viral load in mild to moderate COVID‐19. Safety and immunogenicity of an BBV152: whole‐virion inactivated SARS‐CoV‐2 inactivated SARS‐CoV‐2 Lancet Safety and immunogenicity of an Vaccine vaccine, BBV152: a vaccine formulated with a toll‐ 21‐Jan‐21 Infectionus inactivated SARS‐CoV‐2 vaccine, BBV152: India Ella R., et al. NCT04471519 BVB152 vaccine Phase I double‐blind, like receptor 7/8 agonist diseases a double‐blind, randomised, phase 1 trial randomised, phase 1 molecule adsorbed to alum trial ‐ The Lancet (AlgelIMDG) or alum (Algel) Infectious Diseases

Effect of tocilizumab on clinical outcomes Does tocilizumab improves at 15 days in patients with severe or https://www.bmj.com/c 20‐Jan‐21 BMJ RCT Brazil Veiga, V.C. et al. NCT04403685 tocilizumab clinical outcomes for patients critical coronavirus disease 2019: ontent/372/bmj.n84 with severe or COVID‐19?. randomised controlled tria

Interim Results of a NCT04436276. The safety and Interim Results of a Phase 1–2a Trial of vaccine Phase 1–2a Trial of 13‐Jan‐21 NEJM USA Sadoff J., et al. opens in new Ad26.COV2.S vaccine immunogenicity profiles of Ad26.COV2.S Covid‐19 Vaccine Phase I/IIa Ad26.COV2.S Covid‐19 tab. Ad26.COV2 Vaccine | NEJM

To assess whether convalescent plasma with high antibody levels https://www.medrxiv.or rather than low antibody expanded Early Safety Indicators of COVID‐19 g/content/10.1101/2020 levels is associated with a 13‐Jan‐21 NEJM access USA Joyner et al. NCT04338360 Convalescent plasma Convalescent Plasma in 5,000 Patients .05.12.20099879v1.full.p lower risk of program df death. Primary outcome: death within 30 days after plasma transfusion.

Short term, high‐dose vitamin D https://pmj.bmj.com/co Do high doses of Postgraduate supplementation for COVID‐19 disease: a ntent/early/2020/11/12 cholecalciferol lead to SARS‐ 11‐Nov‐20 RCT India Rastogi et al. NCT04459247 Vitamin D Medical Journal randomised, placebo‐controlled, study /postgradmedj‐2020‐ CoV‐2 negativity in greater (SHADE study) 139065 proportions?

Safety and immunogenicity of S‐Trimer (SCB‐ https://www.thelancet.c 2019), a protein subunit vaccine candidate for Phase I om/journals/lancet/artic Dose‐finding and adjuvant Multinatio 29‐Jan‐21 The Lancet COVID‐19 in healthy adults: a phase 1, vaccine Richmond et al. le/PIIS0140‐ NCT04405908 S‐Trimer (SCB‐2019) justification of SCB‐2019 nal randomised, double‐blind, placebo‐controlled trial 6736(21)00241‐ vaccine trial 5/fulltext https://www.thelancet.c Safety and efficacy of an rAd26 and rAd5 Phase III om/journals/lancet/artic vector‐based heterologous prime‐boost Gam‐COVID‐Vac Efficacy and safety of Gam‐ 02‐Feb‐21 The Lancet vaccine Russia Logunov et al. le/PIIS0140‐ NCT04530396 COVID‐19 vaccine: an interim analysis of a (Sputnik V) COVID‐Vac randomised controlled phase 3 trial in Russia trial 6736(21)00234‐ 8/fulltext

Early High‐Titer Plasma Early High‐Titer Plasma Does convalescent plasma Therapy to Prevent 06‐Jan‐21 NEJM Therapy to Prevent Severe RCT Argentina Libster R, et al. NCT04479163 Convalescent plasma reduce the development of Severe Covid‐19 in Older Covid‐19 in Older Adults severe respiratory disease? Adults | NEJM

Efficacy, Safety, and https://www.nejm.org/d Immunogenicity of mRNA‐ Efficacy and Safety of the mRNA‐1273 Vaccine ‐ oi/full/10.1056/NEJMoa mRNA‐1273 SARS‐CoV‐ 30‐Dec‐21 NEJM USA Baden LR, et al. NCT04470427 1273 Vaccine in Adults Aged SARS‐CoV‐2 Vaccine phase III 2035389?query=feature 2 Vaccine 18 Years and Older to Prevent d_coronavirus COVID‐19

https://www.medrxiv.or Enisamium is an inhibitor of the SARS‐CoV‐2 Efficacy and safety of RNA polymerase and shows improvement of Multinatio g/content/10.1101/2021 12‐Jan‐21 MedRxiv RCT Holubovska et al. NCT04682873 enisamium enisamium at COVID‐19 recovery in COVID‐19 patients in an interim nal .01.05.21249237v1.full‐ patients analysis of a text

Safety and immunogenicity of SARS‐CoV‐2 Vaccine https://www.medrxiv.or recombinant protein vaccine formulations in Multinatio CoV2 preS dTM Safety and imunogenicity of 20‐Jan‐21 MedRxiv trial phase Goepfert et al. g/content/10.1101/2021 NCT04537208 healthy adults: a randomised, placebo‐ nal vaccine CoV2 preS dTM vaccine controlled, dose‐ranging study I/II .01.19.20248611v1

https://link.springer.co Annals of Pilot trial of high‐dose vitamin C in critically ill Effect of high doses of vitamin 09‐Jan‐21 RCT China Zhang et al. m/article/10.1186/s136 NCT04264533 Vitamin C Intensive Care COVID‐19 patients C 13‐020‐00792‐3

Efficacy and safety of , an oral International https://www.sciencedir RNA‐dependent RNA polymerase Efficacy and safety of Journal of ect.com/science/article/ CTRI/2020/05/0 01‐Feb‐21 inhibitor, in mild‐to‐moderate COVID‐19: RCT India Udwadia et al. favipiravir favipiravir in adults with mild‐ Infectious pii/S120197122032453X 25114 A randomized, comparative, open‐label, to‐moderate COVID‐19 Diseases ?via%3Dihub multicenter, phase 3 clinical trial ISRCTN8995142 Safety and efficacy of the ChAdOx1 nCoV‐ https://www.thelancet.c phase 4, 19 vaccine (AZD1222) against SARS‐CoV‐ om/journals/lancet/artic To test the safety and efficacy I/II/III Multinatio NCT04324606, ChAdOx1 nCoV‐19 08‐Dec‐20 Lancet 2: an interim analysis of four randomised Voysey et al. le/PIIS0140‐ of the ChAdOx1 nCoV‐19 vaccine nal NCT04400838, vaccine controlled trials in Brazil, South Africa, 6736(20)32661‐ vaccine trial and and the UK 1/fulltext NCT04444674

Effect of Baricitinib plus baricitinib (≤14 days) plus Baricitinib plus for Remdesivir for Baricitinib plus remdesivir (≤10 days) vs. 11‐Dec‐20 NEJM RCT USA Kalil A.C., et al NCT04401579 Hospitalized Adults with Covid‐19 Hospitalized Adults with Remdesivir remdesivir alone Covid‐19 | NEJM in hospitalized adults with Covid‐19 To test the safety and efficacy https://www.nejm.org/d Tocilizumab in Patients Hospitalized with of tocilizumab in hospitalized 17‐Dec‐20 NEJM RCT USA Salama et al. oi/10.1056/NEJMoa2030 NCT04372186 tocilizumab Covid‐19 Pneumonia patients with Covid‐19 340 pneumonia

https://assets.researchs Exogenous Surfactant Versus Placebo in quare.com/files/rs‐ the Treatment of Moderate and Severe IRCT200912010 Is surfactant effective in 31‐Dec‐20 Preprint RCT Iran Ghahremani et al. 136365/v1/adcad24b‐ surfactant ARDS in COVID19: The Pilot Study of a 02804N12 COVID‐19 paients? f7ed‐477b‐a235‐ Clinical Trial 235f84f8ce1b.pdf WHO mortality trial of four remdesivir, Repurposed Antiviral repurposed antiviral drugs — hydroxychloroquine Repurposed Antiviral Drugs for Covid‐19 Multinatio WHO Soidarity Trial Drugs for Covid‐19 — remdesivir, 02‐Dec‐20 NEJM RCT NCT04315948 (HCQ), lopinavir, and — Interim WHO Solidarity Trial Results nal Consortium Interim WHO Solidarity hydroxychloroquine (HCQ), beta‐1a Trial Results | NEJM lopinavir, and interferon beta‐ (IFN) 1a (IFN)— in patients mRNA 1273 vaccine Durability of Responses Phase I immunogenicity 3 months Durability of Responses after SARS‐CoV‐2 mRNA‐ 03‐Dec‐20 NEJM vaccine USA Widge A.T., et al. NCT04283461 mRNA 1273 vaccine after second after SARS‐CoV‐2 mRNA1273 Vaccination 1273 Vaccination | trial vaccination NEJM

Safety and immunogenicity of INO‐4800 Phase I https://www.sciencedir EClinicalMedici DNA vaccine against SARS‐CoV‐2: A INO‐4800 DNA Safety and immunogenicity of 24‐Dec‐20 vaccine USA/UK Tebas et al. ect.com/science/article/ NCT04336410 ne preliminary report of an open‐label, vaccine INO‐4800 vaccine trial pii/S2589537020304338 Phase 1 clinical trial

Phase 1/2 trial of SARSCoV‐2 vaccine Safety and exploratory Phase I/II https://www.nature.co ChAdOx1 nCoV‐19 with a booster dose ChAdOx1 nCoV‐19 humoral and cellular 17‐Dec‐20 Nature Med. vaccine UK Barrett J.R., et al. m/articles/s41591‐020‐ NCT04400838 induces multifunctional antibody vaccine AZD1222 immunogenicity of the trial 01179‐4 responses AZD1222 vaccine Interim study results: effects REGN‐COV2, a of high viral loads with REGN‐COV2, a Neutralizing Neutralizing Antibody REGN‐COV2 antibody complications 17‐Dec‐20 NEJM Antibody Cocktail, in RCT USA Weinreich D.M NCT04425629 Cocktail, in Outpatients cocktail and death from coronavirus Outpatients with Covid‐19 with Covid‐19 | NEJM disease 2019 (Covid‐19)‐REGN‐ COV2 Safety and immunogenicity clinical trial of an inactivated SARS‐CoV‐2 vaccine, Phase I/II https://www.medrxiv.or To test the immunogenicity BBV152 (a phase 2, double‐blind, inactivated SARS‐CoV‐ 22‐Dec‐20 preprint ‐ BMJ vaccine India Raches et al. g/content/10.1101/2020 NCT04471519 and safety of BBV152: 3 µg randomised controlled trial) and the 2 vaccine, BBV152 trial .12.21.20248643v1 and 6 µg with Algel‐IMDG. persistence of immune responses from a phase 1 follow‐up report A Neutralizing ACTIV‐3/TICO LY‐ To test the effect of this A Neutralizing Monoclonal Antibody for Monoclonal Antibody 22‐Dec‐20 NEJM RCT Denmark CoV555 Study NCT04501978 LY‐CoV555 antibody in patients who are Hospitalized Patients with Covid‐19 for Hospitalized Patients Group hospitalized with Covid‐19. with Covid‐19 | NEJM To test the effect of Tocilizumab on multi‐organ Efficacy of Tocilizumab in Efficacy of Tocilizumab dysfunction in a phase 3 10‐Dec‐20 NEJM Patients Hospitalized with RCT USA Stone J.H., et al in Patients Hospitalized NCT04356937 tocilizumab randomized controlled trial Covid‐19 with Covid‐19 | NEJM among hospitalized patients with COVID‐19 . https://bmcinfectdis.bio To determine the effect of Effect of Arbidol () on COVID‐ medcentral.com/articles IRCT201807250 14‐Dec‐20 BMC Infect Dis RCT Iran Marzieh et al. Arbidol (Umifenovir) Arbidol (ARB) on COVID‐19 19: a randomized controlled trial. /10.1186/s12879‐020‐ 40596N2 disease. 05698‐w

https://trialsjournal.bio To test the efficacy of Interferon ß‐1a (IFNß‐1a) in COVID‐19 EudraCT 2020‐ medcentral.com/articles Interferon ß‐1a (IFNß‐ Interferon‐β‐1a (IFNβ‐1a), in 23‐Dec‐20 Trials patients (INTERCOP): study protocol for a RCT Italy Bosi et al. 002458‐25, /10.1186/s13063‐020‐ 1a) COVID‐19 patients in an open randomized controlled trial. NCT04449380 04864‐4 label, randomized clinical trial. To evaluate the efficacy and Safety and Efficacy of safety of BNT162b2 is a lipid phase II NCT04368728. Safety and Efficacy of the BNT162b2 the BNT162b2 mRNA nanoparticle–formulated, 10‐Dec‐20 NEJM vaccine USA Polack F.P., et al. opens in new BNT162b2 vaccine mRNA Covid‐19 Vaccine Covid‐19 Vaccine | nucleoside‐modified RNA trial tab NEJM vaccine that encodes a prefusion stabilized, https://academic.oup.co Journal of and for the m/jac/advance‐ IRCT202004030 Is sofosbuvir/daclatasvir 18‐Dec‐20 Antimicrobial treatment of COVID‐19 outpatients: a RCT Iran Roozbeh et al. article/doi/10.1093/jac/ sofosbuvir, daclatasvir 46926N1 effective in COVID‐19 patiets? Chemotherapy double‐blind, randomized controlled trial dkaa501/6041772?login =true https://journals.lww.co m/ccejournal/Fulltext/2 To asses the efficacy and Intravenous Immunoglobulin Plus 16 November Critical Care George Sakoulas, et 020/11000/Intravenous safety of IV immunoglobulin in Methylprednisolone Mitigate Respiratory RCT USA NCT04411667 Immunoglobulins 2020 Explorations al. _Immunoglobulin_Plus_ hospitalized COVID‐19 Morbidity in Coronavirus Disease 2019 Methylprednisolone.14. patients. aspx To evaluate the effect of Biological Trace Do Zinc Supplements Enhance the Clinical https://link.springer.co combining 23 November Sherief Abd‐ Zinc, Element Efficacy of Hydroxychloroquine?: a RCT Egypt m/article/10.1007/s120 NCT04447534 chloroquine/hydroxychloroqui 2020 Elsalam, et al. Hydroxychloroquine Research Randomized, Multicenter Trial 11‐020‐02512‐1 ne and zinc in the treatment of COVID‐19 patients. Effect of Vitamin D3 Supplementation vs To determine if vitamin D3 https://www.medrxiv.or Placebo on Hospital Length of Stay in supplementation can reduce g/content/10.1101/2020 17‐Nov MedRxiv Patients with Severe COVID‐19: A RCT Brazil Murai et al. NCT04449718 Vitamin D3 hospital length of stay in .11.16.20232397v1.full.p Multicenter, Double‐blind, Randomized 3 hospitalized patients with df Controlled Trial severe COVID‐19? To determine whether a https://www.medrxiv.or single, 180 mcg subcutaneous Peginterferon Lambda‐1a for treatment g/content/10.1101/2020 Peginterferon Lambda‐ dose of Peginterferon Lambda‐ 23‐Nov MedRxiv of outpatients with uncomplicated COVID‐ RCT USA Jagannathan et al. NCT04331899 .11.18.20234161v1.full.p 1a 1a (Lambda) could shorten the 19: a randomized placebo‐controlled trial df duration of viral shedding or symptoms in patients with To evaluate the efficacy of https://www.medrxiv.or convalescent plasma with high Prevention of severe COVID‐19 in the g/content/10.1101/2020 titers of SARS‐CoV2 antibody 21‐Nov MedRxiv RCT Argentina Libster et al. NCT04479163 Convalescent plasma elderly by early hightiter plasma .11.20.20234013v1.full.p administered within 72 hours df of mild symptoms to elderly patients with Covid‐19 To estimate the efficacy and A two‐arm, randomized, controlled, multi‐ https://www.medrxiv.or safety of Itolizumab in the centric, open‐label Phase‐2 study to g/content/10.1101/2020 CTRI/2020/05/0 treatment of cytokine release 02‐Dec MedRxiv evaluate the efficacy and safety of RCT India Kumar et al. Itolizumab .12.01.20239574v1.full.p 24959 syndrome in patients with Itolizumab in moderate to severe ARDS df moderate to severe acute patients due to COVID‐19 respiratory distress syndrome 5‐Alpha‐Reductase Inhibitors Reduce To determine if 5‐alpha‐ https://www.medrxiv.or Remission Time of COVID‐19: Results reductase inhibitors (5ARis) g/content/10.1101/2020 18‐Nov MedRxiv From a Randomized Double Blind Placebo RCT Brazil, USA Cadegiani et al. NCT04446429 Dutasteride are a beneficial treatment for .11.16.20232512v1.full.p Controlled Interventional Trial in 130 COVID‐19 if given after SARS‐ df SARSCoV‐2 Positive Men CoV‐2 infection https://reader.elsevier.c To test the effect Pentoxifylline decreases serum LDH levels om/reader/sd/pii/S1567 Pentoxifylline (PTX) on International and increases lymphocyte count in COVID‐ 576920336766?token=E parameters such as LDH, 11‐Nov Immunopharma RCT Mexico Maldonado et al. COF‐002495 Pentoxifylline 19 patients: Results from an external pilot DD4B561C8D7F700793B lymphocyte count, days of cology study 55AFFA9EE8F0CD28010 hospitalization, mortality, and BE3E0CADC0EF90237E4 the need for intubation on hydroxychloroquine, https://www.nejm.org/d Repurposed Antiviral Drugs for Covid‐19 Multinatio WHO Solidarity Trial ISRCTN8397115 lopinavir/, effects of drugs on in‐hospital 02‐Dec‐20 NEJM RCT oi/10.1056/NEJMoa2023 — Interim WHO Solidarity Trial Results nal Consortium 1, NCT04315948 interferon beta1, mortality 184 remdesivir

Does postexposure A Cluster‐Randomized Trial of https://www.nejm.org/d prophylaxis with 24‐Nov‐20 NEJM Hydroxychloroquine for Prevention of RCT Spain Mitjà et al. oi/10.1056/NEJMoa2021 NCT04304053 Hydroxychloroquine hydroxychloroquine prevent Covid‐19 801 SARS‐CoV‐2 infection?

Is treatment with https://www.nejm.org/d convalescent plasma A Randomized Trial of Convalescent 24‐Nov‐20 NEJM RCT Argentina Simonovich et al. oi/10.1056/NEJMoa2031 NCT04383535 Convalescent plasma associated with improved Plasma in Covid‐19 Severe Pneumonia 304 clinical outcomes in COVID‐19 patients? Safety and immunogenicity of ChAdOx1 https://www.sciencedir nCoV‐19 vaccine administered in a prime‐ phase II/III NCT04400838, Safety and immunogenicity of ect.com/science/article/ 19‐Nov‐20 The Lancet boost regimen in young and old adults vaccine UK Ramasamy et al. ISRCTN ChAdOx1 vaccine ChAdOx1 vaccine in young and pii/S0140673620324661 (COV002): a single‐blind, randomised, trial 15281137 old adults ?via%3Dihub controlled, phase 2/3 trial Safety, tolerability, and immunogenicity https://www.sciencedir of an inactivated SARS‐CoV‐2 vaccine in Safety, tolerability and Lancet Infect. I/II vaccine ect.com/science/article/ 18‐Nov‐20 healthy adults aged 18–59 years: a China Zhang et al. NCT04352608 CoronaVac vaccine immunogenicity of CoronaVac Dis. trial pii/S1473309920308434 randomised, double‐blind, placebo‐ vaccine ?via%3Dihub controlled, phase 1/2 clinical trial.

Randomized controlled trial of https://www.medrxiv.or Pilot study designed to inform convalescent plasma therapy against Bahrain, g/content/10.1101/2020 04‐Nov MedRxiv RCT Al Qahtani et al. NCT04356534 Convalescent plasma the design of a definitive standard therapy in 2 patients with Ireland .11.02.20224303v1.full.p phase 3 clinical trial. severe COVID‐19 disease df

https://www.medrxiv.or To evaluate a single Peginterferon‐lambda for the treatment g/content/10.1101/2020 subcutaneous injection of 12/11/2020 MedRxiv RCT Canada Feld et al. NCT04354259 Peginterferon of COVID‐19 in outpatients .11.09.20228098v1.full.p peginterferon‐lambda in df outpatients with COVID‐19. https://reader.elsevier.c Evaluating the effects of Intravenous om/reader/sd/pii/S1567 To investigate the potential International Immunoglobulin (IVIg) on the 576920336729?token=1 IRCT201512270 Intravenous usefulness of IVIg for the 13‐Nov Immunopharma RCT Iran Tabarsi et al. management of severe COVID‐19 cases: A 3C23CAB7F2F51222936F 25726N20 Immunoglobulin management of severe cases cology randomized controlled trial 6967643ECEC50F680C6C of Covid‐19. 1B600298B1211225F0D To evaluate the therapeutic Randomized Controlled Open Label Trial International https://www.sciencedir effectiveness of favipiravir on the Use of Favipiravir Combined with 9 November 2020 Journal of ect.com/science/article/ Favipiravir, interferon combined with inhaled Inhaled Interferon beta‐1b in Hospitalized RCT Oman Faryal Khamis, et al. NA (preprint) Infectious pii/S1201971220323195 beta‐1b interferon beta‐1b in adult Patients with Moderate to Severe COVID‐ Diseases ?via%3Dihub patients hospitalized with 19 Pneumonia moderate to severe COVID‐19 https://academic.oup.co Clinical Randomized, double‐blinded and placebo‐ Phase 2 Assess the safety and m/cid/advance‐ Preprint Infectious controlled phase II trial of an inactivated vaccine China Yanchun Che, et al. NCT04412538 Inactivated vaccine immunogenitcity of this article/doi/10.1093/cid/ Diseases SARS‐CoV‐2 vaccine in healthy adults trial inactiviated vaccine ciaa1703/5962856 To evaluate the efficacy of PEP International Post‐exposure prophylaxis with https://www.sciencedir with HCQ for the prevention 6 November 2020 Journal of hydroxychloroquine for the prevention of Deba Prasad ect.com/science/article/ of COVID‐19 in asymptomatic RCT India NCT04408456 Hydroxychloroquine (in press) Antimicrobial COVID‐19, a myth or a reality? The PEP‐ Dhibar, et al. pii/S0924857920304350 non‐HCW in‐ dividuals who Agents CQ Study ?via%3Dihub were at risk for SARS‐CoV‐2 infection To assess the safety, tolerability, and Phase 1 trial of a Candidate Recombinant Phase 1 https://www.medrxiv.or immunogenicity of CoVLP at Preprint MedRxiv Virus‐Like Particle Vaccine for Covid‐19 vaccine Canada Brian J Ward, et al. g/content/10.1101/2020 NCT04450004 CoVLP vaccine three dose levels Disease Produced in Plants Trial .11.04.20226282v1 unadjuvanted or adjuvanted with either CpG 1018 or AS03 To evaluate the efficacy and An open‐label, randomized trial of the https://www.sciencedir E‐Clinical safety in patients with combination of IFN‐κ plus TFF2 with ect.com/science/article/ ChiCTR2000030 27 October 2020 Medicine RCT China Weihui Fu, et al. IFN‐κ plus TFF2 moderate COVID‐19 f the standard care in the treatment of pii/S2589537020302911 262 (Lancet) combination of IFN‐κ plus patients with moderate COVID‐19 ?via%3Dihub TFF2 Safety and efficacy of inhaled nebulised https://www.thelancet.c The Lancet interferon beta‐1a (SNG001) for om/journals/lanres/artic 2020‐001023‐ Efficacy and safety of inhaled 12‐Nov‐20 Respiratory treatment of SARS‐CoV‐2 infection: a RCT UK Monk et al. le/PIIS2213‐ 14, INF‐beta 1a nebulised interferon beta‐1a Medicine randomised, double‐blind, placebo‐ 2600(20)30511‐ NCT04385095 controlled, phase 2 trial 7/fulltext Determine whether Fluvoxamine vs Placebo and Clinical fluvoxamine, given during https://jamanetwork.co Deterioration in Outpatients With mild COVID‐19 illness, 12‐Nov‐20 JAMA RCT USA Lenze et al. m/journals/jama/article‐ NCT04342663 Fluvoxamine Symptomatic COVID‐19A Randomized prevents clinical deterioration abstract/2773108 Clinical Trial and decreases the severity of disease

Antiviral effect of high‐dose ivermectin in https://papers.ssrn.com Does ivermectin reduce the Preprint The Lancet adults with COVID‐19: a pilot randomised, RCT Argentina Krolewiecki et al. /sol3/papers.cfm?abstra NCT004381884 Ivermectin viral load? controlled, open label, multicentre trial ct_id=3714649

Efficacy of Convalescent Plasma Therapy https://www.medrxiv.or To compare the efficacy and compared to Fresh Frozen Plasma in g/content/10.1101/2020 safety of convalescent plasma 27‐Oct MedRxiv RCT India Bajpai et al. NCT04346446 Convalescent plasma Severely ill COVID‐19 Patients: A Pilot .10.25.20219337v1.full.p with fresh frozen plasma (FFP) Randomized Controlled Trial. df in severe COVID‐19 patients

To evaluate the efficacy and https://www.medrxiv.or A placebo‐controlled double blind trial of Dubée et al. for the safety of hydroxychloroquine g/content/10.1101/2020 21‐Oct MedRxiv hydroxychloroquine in mild‐to‐moderate RCT France HYCOVID study NCT04325893 Hydroxychloroquine in adult patients with mild‐to‐ .10.19.20214940v1.full.p COVID‐19 group moderate COVID‐19 at risk of df worsening. To evaluate whether early https://www.medrxiv.or Early use of nitazoxanide in mild Covid‐19 nitazoxanide therapy would g/content/10.1101/2020 23‐Oct MedRxiv disease: randomized, placebo controlled RCT Brazil Rocco et al. NCT04552483 Nitazoxanide be effective in accelerating .10.21.20217208v1.full.p trial symptom resolution in df patients with mild COVID‐19. To test the combinational Controlled randomized clinical trial on https://www.medrxiv.or therapy of Ivermectin and using Ivermectin with Doxycycline for g/content/10.1101/2020 Ivermectin + 27‐Oct MedRxiv RCT Iraq Hashim et al. NCT04591600 Doxycycline in treating COVID‐ treating COVID‐19 patients in Baghdad, .10.26.20219345v1.full.p Doxycycline 19 patients at different stages Iraq df of the disease. To assess the efficacy and Treatment with human umbilical cord‐ https://www.medrxiv.or safety of human umbilical derived mesenchymal stem cells for human umbilical cord‐ g/content/10.1101/2020 cord‐mesenchymal stem cells 21‐Oct MedRxiv COVID‐19 patients with lung damage: a RCT China Shi et el. NCT04288102 derived mesenchymal .10.15.20213553v2.full.p (UC‐MSCs) to treat severe randomised, double‐blind, placebo‐ stem cells df COVID‐19 patients with lung controlled phase 2 trial damage. To determine safety and Umbilical Cord Mesenchymal Stem Cells https://papers.ssrn.com human umbilical cord‐ explore efficacy of Umbilical 26‐Oct Lancet pre‐print for COVID‐19 ARDS: A Double Blind, RCT USA Lanzoni et al. /sol3/papers.cfm?abstra NCT04355728 derived mesenchymal Cord (UC)‐MSC infusions in Phase 1/2a, Randomized Controlled Trial ct_id=3696875 stem cells COVID‐19 ARDS.

To determine whether https://academic.oup.co Sofosbuvir/daclatasvir regimens for the sofosbuvir/daclatasvir‐based J Antimicrob Meta‐ m/jac/advance‐ 01‐Nov treatment of COVID‐19: an individual UK/Iran Simmons et al. N/A sofosbuvir/daclatasvir regimens improve clinical Chemother analysis article/doi/10.1093/jac/ patient data meta‐analysis outcomes of patients with dkaa418/5924537 moderate or severe COVID‐19.

To evaluate the efficacy and https://papers.ssrn.com Phase 3 Trial of Coronavir (Favipiravir) in safety of favipiravir for 26‐Oct Lancet pre‐print RCT Russia Ruzhentsova et al. /sol3/papers.cfm?abstra NCT04501783 Favipiravir Patients with Mild to Moderate COVID‐19 treatment of mild to ct_id=3696907 moderate COVID‐19

Treatment of Coronavirus Disease 2019 https://www.sciencedir Efficacy of COVID‐19 Imunopatholog Patients with Convalescent Plasma ect.com/science/article/ convalescent plasma 01‐Nov‐20 y and infectious RCT USA Salazar et al. Convalescent plasma Reveals a Signal of Significantly pii/S0002944020303709 transfusion for severe and/or diseases Decreased Mortality ?via%3Dihub critical COVID‐19.

https://www.nejm.org/d Efficacy of Tocilizumab in Patients Does tocilizumab prevent 21‐Oct‐20 NEJM RCT USA Stone et al. oi/pdf/10.1056/NEJMoa NCT04356937 Tocilizumab Hospitalized with Covid‐19 intubation or death? 2028836

To determine whether Effect of Tocilizumab vs Usual Care in https://jamanetwork.co tocilizumab (TCZ) improves JAMA Internal Adults Hospitalized With COVID‐19 and m/journals/jamainternal 20‐Oct‐20 RCT France Hermine et al. NCT04331808 Tocilizumab outcomes of patients Medicine Moderate or Severe Pneumonia: A medicine/fullarticle/277 hospitalized with moderate‐to‐ Randomized Clinical Trial 2187 severe COVID‐19 pneumonia

Effect of Tocilizumab vs Standard Care on https://jamanetwork.co NCT04346355; JAMA Internal Clinical Worsening in Patients m/journals/jamainternal EudraCT To evaluate the effect of early 20‐Oct‐20 RCT Italy Salvarani et al. Tocilizumab Medicine Hospitalized With COVID‐19 PneumoniaA medicine/fullarticle/277 Identifier: 2020‐ tocilizumab administration Randomized Clinical Trial 2186 001386‐37.

International Journal of Randomize https://pharmascope.or To evaluate the efficacy of Efficacy of umifenovir in the treatment of 01‐Oct‐20 Research in d clinical Kyrgizstan Yethindra et al. g/ijrps/article/view/283 NA Umifenovir umifenovir in mild and mild and moderate covid‐19 patients Pharmaceutical study 9/6116 moderate COVID‐19 patients Sciences

To evaluate the efficacy of https://www.nejm.org/d Remdesivir for the Treatment of Covid‐19 John H. Beigel, et remdesivir in shortening time 8 October 2020 NEJM RCT USA oi/10.1056/NEJMoa2007 NCT04280705 Remdesivir — Final Repor al. to recovery in hospitalized 764 COVID‐19 patients.

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pharmacok To establish best‐evidence to Chloroquine dosing recommendations for https://ascpt.onlinelibra Clin Pharmacol inetic Netherland inform pediatric Chloroquine 22 April 2020 pediatric COVID‐19 supported by Verscheijden et al. ry.wiley.com/doi/10.100 N/A Chloroquine Ther. (PBPK) s doses for children infected modeling and simulation. 2/cpt.1864 model with COVID‐19 Effect of High vs Low Doses of Chloroquine Diphosphate as Adjunctive https://jamanetwork.co To evaluate the safety & JAMA Network Therapy for Patients Hospitalized With m/journals/jamanetwor efficacy of different dosages 24 April 2020 RCT Brazil Borba et al NCT04323527 Chloroquine Open Severe Acute Respiratory Syndrome kopen/fullarticle/27654 of chloroquine in patients with Coronavirus 2 (SARS‐CoV‐2) Infection: A 99 severe COVID‐19. Randomized Clinical Trial. A Randomized, Single‐blind, Group https://www.medrxiv.or To evaluate the clinical sequential, Active‐controlled Study to g/content/10.1101/2020 ChiCTR2000029 efficacy and safety of α‐Lipoic 21 April 2020 medRxiv evaluate the clinical efficacy and safety of RCT China Zhong et al. α‐Lipoic acid (ALA) .04.15.20066266v1.full.p 851 acid (ALA) for critically ill α‐Lipoic acid for critically ill patients with df patients with COVID‐19. coronavirus disease 2019(COVID‐19) To systematically retrieve and Rapid summarize the current Effectiveness and Safety of https://www.medrxiv.or review and evidence of the effectiveness 22 April 2020 medRxiv Glucocorticoids to Treat COVID‐19: A China Shuya Lu et al g/content/10.1101/2020 N/A Glucocorticoids meta‐ and safety of glucocorticoid Rapid Review and Meta‐Analysis .04.17.20064469v1 analysis therapy for patients with COVID‐19 https://www.medrxiv.or To assess the effectiveness of A systematic review of Anakinra, Anakinra, Systematic g/content/10.1101/2020 specific interleukin‐1 and ‐6 26 April 2020 MedRxiv Tocilizumab, Sarilumab and Siltuximab for UK Khan et al N/A Tocilizumab, review .04.23.20076612v1.full.p inhibitors for the treatment of coronavirus‐related infections Sarilumab, Siltuximab df coronavirus‐related infections. https://www.cytodyn.co Preliminary m/newsroom/press‐ Southern California Patients Treated with results releases/detail/415/sout 13 April 2020 Press release Leronlimab for COVID‐19 under from USA CytoDyn INC. NA leronlimab Could leronlimab be effective? hern‐california‐patients‐ Emergency IND clinical trial treated‐with‐leronlimab‐ for

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No evidence of rapid antiviral clearance Prospectiv https://www.sciencedir Is hydroxychloroquine Médécine et or clinical ben‐efit with the combination e ect.com/science/article/ Hydroxychloroquine, effecitve for viral clearance Preprint Maladies of hydroxychloroquine and azithromycin France JM Molina et al. NA virological pii/S0399077X20300858 azithromycin when reproducing the study Infectieuses in patients with severe COVID‐19 assay ?via%3Dihub of Gautrel et al.? infection Grant from the https://www.sciencedir National The effect of corticosteroid treatment on Evaluate the influence of Accepted 31 Journal of Meta‐ ect.com/science/article/ Natural Science patients with coronavirus infection: a China Zhenwei Yang, et al. Corticosteroids corticosteroids in patients March 2020 Infection analysis pii/S0163445320301912 Foundation of systematic review and meta‐analysis with coronavirus. ?via%3Dihub China (Jing Liu, grant no.

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https://www.sciencedir A systematic review on the efficacy and Summary of the existing the Journal of Systematic Andrea Cortegiani, ect.com/science/article/ 10 March 2020 safety of chloroquine for the treatment of Italy NA Chloroquine evidence on chloroquine for Critical Care review et al. pii/S0883944120303907 COVID‐19 the treatment of COVID‐19 ?via%3Dihub Systematic review of the Systematic review of the efficacy and clinical outcomes of using Journal https://onlinelibrary.wil safety of antiretroviral drugs against Systematic antiretroviral drugs for the Preprint International Switzerland N Ford et al. ey.com/doi/10.1002/jia2 NA Antiretroviral drugs SARS, MERS, or COVID‐19: initial review prevention and treatment of AIDS Society .25489 assessment coronaviruses and planned clinical trials Ethics Investigate the effects of 6‐ committees of week respiratory Complementary Respiratory rehabilitation in elderly Non‐ https://www.sciencedir Hainan General Respiratory rehabilitation training on 30 March 2020 Therapies in patients with COVID‐19: A randomized interventio China Kai Liu, et al. ect.com/science/article/ Hospital and rehabilitation training respiratory function, QoL, Clinical Practice controlled study nal RCT pii/S1744388120304278 Huanggang mobility and psychological Central Hospital function in elderly patients Investigate the effect of Complementary Effects of progressive muscle relaxation Non‐ https://www.sciencedir Progressive muscle progressive muscle relaxation 6 March 2020 Therapies in on anxiety and sleep quality in patients interventio China Kai Liu, et al. ect.com/science/article/ NA relaxation (sleep on anxiety and sleep quality of Clinical Practice with COVID‐19 nal RCT pii/S1744388120302784 therapy) COVID‐19 patients

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The potential of low molecular weight https://www.medrxiv.or heparin to mitigate cytokine storm in Retrospecti 07 April 2020 MedRxiv China Chen Shi et al. g/content/10.1101/2020 not found enoxaparin Efficacy of enoxaparin severe covid‐19 patients: a retrospective ve CT .03.28.20046144v2 clinical study No evidence of clinical efficacy of hydroxychloroquine in patients https://www.medrxiv.or To assess the effectiveness of hospitalised for COVID‐19 infection and Retrospecti Matthieu Mahévas g/content/10.1101/2020 14 April 2020 MedRxiv France NA Hydroxychloroquine Hydroxychloroquine in requiring oxygen: results of a study using ve analysis et al. .04.10.20060699v1.full.p patients with severe Covid‐19 routinely collected data to emulate a df target trial Grants: National Science and https://jamanetwork.co Is plasma from convalescente Treatment of 5 critically ill patients with Observatio Technology 27 March 2020 JAMA China C Shen, et al. m/journals/jama/fullarti Convalescent plasma patients beneficial for COVID‐19 with convalescent plasma nal study Major Project cle/2763983 critically ill COVID19 patients? (2018ZX107110 01, Proceedings of the National Observatio Is treatment with The feasibility of convalescent plasma https://www.pnas.org/c Academy of nal/retrosp ChiCTR2000030 convalescent plasma safe and 6 April 2020 therapy in severe COVID‐19 patients: a China Kai Duan et al ontent/early/2020/04/0 Convalescent plasma Sciences of the ective 048 beneficial for COVID19 pilot study 2/2004168117 United States of control patients? America Compare medical masks to Influenza and Medical Masks vs N95 Respirators for N95 respirators in preventing https://onlinelibrary.wil other Preventing COVID‐19 in Health Care Systematic Jessica J Bartoszko, N95 respirators vs laboratory confirmed viral Preprint Canada ey.com/doi/pdf/10.1111 NA Respiratory Workers ‐ A Systematic Review and Meta‐ review et al. surgical masks infection and respiratory /irv.12745 Viruses Analysis of Randomized Trials illness including coronavirus specifically in health care https://www.cambridge. Is attending one live training RANDOMIZED TRIAL OF INSTRUCTOR‐LED Disaster org/core/journals/disast session or watching video TRAINING VERSUS VIDEO LESSON IN Medicine and er‐medicine‐and‐public‐ Training on personal trainings over a month more Preprint TRAINING HEALTH CARE PROVIDERS IN RCT Denmark L Christensen et al NA Public Health health‐ protective equipment effective for training on PROPER DONNING AND DOFFING OF Preparedness preparedness/article/ra downing and doffing personal PERSONAL PROTECTIVE EQUIPMENT ndomized‐trial‐of‐ protective equipment? Performance of VivaDiagTM COVID‐19 Journal of https://onlinelibrary.wil To assess an easy to perform IgM/IgG Rapid Test is inadequate for Diagnostic Irene Cassantini et Diagnostic serological Preprint Medical Italy ey.com/doi/epdf/10.100 NA serological assay for diagnosis diagnosis of COVID‐19 in acute patients assay al. assay Virology 2/jmv.25800 of COVID19 referring to emergency room department DOI: 10.1128/JC M.00461‐20; Evaluation of Nucleocapsid and Spike https://jcm.asm.org/con Joural of Clinical Diagnostic Hospital Ethics Diagnostic serological Evaluate the diagnostic Preprint Protein‐based ELISAs for detecting China Wanbing Liu, et al. tent/early/2020/03/27/J Microbiology assay Committee of assay feasibility of two ELISA assays antibodies against SARS‐CoV‐2 CM.00461‐20 the General Hospital of the Article originally Australian New published in 2015; A cluster randomised trial of cloth masks Zealand Clinical To compare the efficacy of Australia https://bmjopen.bmj.co medical masks, cloth authors added BMJ Open compared with medical masks in RCT MacIntyre CR et al. Trials Registry: cloth masks to medical masks /Vietnam m/content/5/4/e006577 masks comment on healthcare workers ACTRN1261000 in hospital healthcare workers 30/03/2020 0887077.

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https://www.sciencedir Arbidol combined with LPV/r versus LPV/r Retrospecti Arbidol and lopinavir‐ritonavir Journal of ect.com/science/article/ Lopinavir/ritonavir, 11 March 2020 alone against Corona Virus Disease 2019: ve cohort China Lisi Deng NA compared to lopinavir‐ Infection pii/S0163445320301134 Arbidol A retrospective cohort study study ritonavir only? ?via%3Dihub What is the efficacy and safety High‐flow nasal‐oxygenation‐ assisted https://bjanaesthesia.or of high‐flow nasal oxygenation British Journal fibreoptic tracheal intubation in critically g/article/S0007‐ ChiCTR2000029 High‐flow nasal during fibreoptic In press RCT China Cai‐Neng Wu et al. of Anaesthesia ill patients with COVID‐19 pneumonia: a 0912(20)30135‐ 658 oxygnation bronchoscopic intubation in prospective randomised controlled trial 5/fulltext critically ill patients with COVID‐19?

Chinese Journal Efficacy of lopinavir, ritonavir and Arbidol 2020 Pre‐print Retrospecti http://rs.yiigle.com/yufa Lopinavir/ritonavir, Efficacy of lopinavir/ritonavir of Infectious for the treatment of new coronavirus China Chen Jun et al. NA online ve analysis biao/1182592.htm Arbidol and arbidol Diseases, pneumonia

Journal of Zhejiang http://www.zjujournals. A pilot study of hydroxychloroquine in University com/med/CN/10.3785/j. Role of hydroxychloroquine on 2020 treatment of patients with common RCT China Chen Jun et al. NCT04261517 Hydroxychloroquine (Medical issn.1008‐ respiratory viral loads coronavirus disease‐19 (COVID‐19) Science) 2020 , 9292.2020.03.03 Vol. 49 Issue Assess the efficacy and safety Meplazumab treats COVID‐19 of meplazumab, a humanized https://doi.org/10.1101/ 2020 Pre‐print MedRxiv pneumonia: an open‐labelled, concurrent CT China Huijie Bian et al. NCT 04275245 Meplazumab anti‐CD147 antibody, as add‐ 2020.03.21.20040691 controlled add‐on clinical trial on therapy in patients with COVID‐19 pneumonia.

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