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2 | 0 Best Practices - Expand the formula bar so that you don't miss the additional info found in some of the cells. Reference the image to the right for more help. - Use filters to explore and organize the information for your own use. When accessing through this view-only link, filters are temporary to that search/find. - This document is also available for download under the File tab. - To find the latest additions or updates to the tracker, command+F or control+F and search for an asterisk. All cells with new information have an added at the end. | Last Update: May 21, 2020 | 12:37 pm ET © 2020 Milken Institute00 2020 | |||||||||||
3 | Treatment vs. Vaccine | Product Category | Product Description | Stage of Development | Anticipated Next Steps | Clinical Trials for COVID-19 | Developer / Researcher | Funder | Published Results | Clinical Trials for Other Diseases (T only) Related Use / Platform (V Only) | FDA-Approved Indications | Sources | Date Last Updated |
4 | Treatment | Antibodies | Polyclonal hyperimmune globulin (H-IG), unbranded | Pre-clinical | Phase 1 trials start in summer 2020. To patients between December 2020 and December 2021 | CoVIg-19 Plasma Alliance (Takeda, CSL Behring, Biotest AG, Bio Products Laboratory, LFB, and Octapharma, ADMA Biologics, BioPharma Plasma, GC Pharma, Sanquin)/ National Institute of Allergy and Infectious Disease (NIAID)/ Microsoft (CoVIg-19 PlasmaBot) | N/A | Sources | 5/10/2020 | ||||
5 | Treatment | Antibodies | Antibodies from mice, REGN3048-3051, against the spike protein | Pre-clinical | Start Phase 1 June 2020 | Regeneron | Biomedical Advanced Research and Development Authority (BARDA) | N/A | Sources | Prior to 4/20/2020 | |||
6 | Treatment | Antibodies | CT-P59; Antibodies from recovered COVID-19 patients | Pre-clinical | Start Phase 1 in July 2020 | Celltrion | The Korea Health Industry Development Institute | N/A | Sources | 5/14/2020 | |||
7 | Treatment | Antibodies | Super-antibody or antibody cocktail to target potential mutations of SARS-CoV-2 | Pre-clinical | Celltrion | N/A | Sources | Prior to 4/20/2020 | |||||
8 | Treatment | Antibodies | COVI-SHIELD antibody cocktail that binds to three different epitopes | Pre-clinical | Start Phase 2 trial 3Q 2020 | Sorrento Therapeutics/ Mount Sinai Health System | N/A | Sources | 5/20/2020 | ||||
9 | Treatment | Antibodies | Antibodies from recovered COVID-19 patients | Pre-clinical | Kamada/ Kedrion Biopharma | N/A | Sources | 5/4/2020 | |||||
10 | Treatment | Antibodies | VIR-7831 and VIR-7832, antibodies from recovered SARS patients | Pre-clinical | Start Phase 2 ~ July-September 2020 | Vir Biotechnology/GSK/ Samsung/WuXi Biologics/Biogen | N/A | Sources | 5/20/2020 | ||||
11 | Treatment | Antibodies | Antibodies from recovered COVID-19 patients | Pre-clinical | Start Phase 1 in late July 2020 | Eli Lilly/Ab-Cellera (NIH Vaccines Research Center) | Defense Advanced Research Projects Agency/ Government of Canada (ISED Strategic Innovation Fund) | N/A | Sources | 5/5/2020 | |||
12 | Treatment | Antibodies | COVID-19 Immunoglobulin, plasma derived | Pre-clinical | CSL Behring Australia | N/A | Sources | 5/10/2020 | |||||
13 | Treatment | Antibodies | Avastin (bevacizumab), vascular endothelial growth factor inhibitor | Clinical | Phase 2/3 studies recruiting April 2020 | NCT04275414 NCT04305106 NCT04344782 | Numerous trials with Chinese research sponsors; Roche | FDA-approved since 2004, approved to treat certain types of cancer | Sources | 4/27/2020 | |||
14 | Treatment | Antibodies | PD-1 blocking antibody; Thymosin | Clinical | Phase 2 study not yet recruiting | NCT04268537 ChiCTR2000030028 | Numerous trials with Chinese research sponsors | Unknown | Sources | 4/27/2020 | |||
15 | Treatment | Antibodies | Opdivo (nivolumab), PD-1 blocking antibody | Clinical | Phase 2 study not yet recruiting | NCT04356508 NCT04333914 | University of Hong Kong (BMS) | FDA-approved since 2014, approved to treat melanoma and squamous non-small cell lung cancer | Sources | 4/27/2020 | |||
16 | Treatment | Antibodies | leronlimab (PRO 140), a CCR5 antagonist | Clinical / Compassionate Use | Phase 2 trial started in April 2020; Phase 2b/3 trial starts April 2020 | NCT04343651 NCT04347239 | CytoDyn | CytoDyn | Treatment of HIV/AIDS, Graft versus Host Disease, Non-Alcoholic Steatohepatitis, and numerous cancers | N/A | Sources | Prior to 4/20/2020 | |
17 | Treatment | Antibodies | AiRuiKa (camrelizumab), anti-programmed cell death protein (PD-1) antibody | Clinical | No trial updates since February 2020 | ChiCTR2000029806 | Wuhan Jinyintan Hospital | Treatment of certain cancers | N/A | Sources | 4/27/2020 | ||
18 | Treatment | Antibodies | Kevzara (sarilumab), interleukin-6 receptor antagonist | Clinical | Started phase 2/3 in March 2020; preliminary Phase 2 results released April 27, 2020, trial continuing for only critical patients, Phase 3 (US) results expected June 2020, Phase 3 (ex-US) results expected 3Q 2020 | NCT04315298 NCT04321993 NCT04341870 NCT04324073 NCT04327388 NCT04322773 NCT04345289 NCT02735707 NCT04357808 NCT04357860 NCT04359901 | Sanofi/Regeneron; Feinstein Institutes; REMAP-CAP global trial | Biomedical Advanced Research and Development Authority (BARDA) | medRxiv (https://doi.org/10.1101/2020.04.23.20076612) Regeneron (https://newsroom.regeneron.com/index.php/news-releases/news-release-details/regeneron-and-sanofi-provide-update-us-phase-23-adaptive) ChinaXiv (http://www.chinaxiv.org/abs/202003.00026) medRxiv (https://doi.org/10.1101/2020.05.14.20094144) | FDA-approved since 2017, approved to treat rheumatoid arthritis | Sources | 5/20/2020 | |
19 | Treatment | Antibodies | Actemra (tocilizumab), interleukin-6 receptor antagonist | Clinical | Roche studies could be completed May or June 2020; Phase 2 open label study in Italy active (April 2020), Phase 3 studies recruiting April 2020, some results from open label study in France released April 2020 | NCT04317092 NCT04320615 NCT04310228 ChiCTR2000030894 NCT04306705 ChiCTR2000030442 ChiCTR2000029765 NCT04322773 NCT04345445 NCT04331795 NCT04332094 NCT04346355 NCT04359667 NCT04332913 NCT04335071 NCT04356937 NCT04361032 NCT04315480 NCT04339712 NCT04333914 NCT04361552 NCT04330638 NCT04331808 NCT02735707 NCT04349410 NCT04363736 NCT04372186 NCT04363853 | Numerous trials with global research sponsors; Roche; REMAP-CAP | Biomedical Advanced Research and Development Authority (BARDA) | ChinaXiv (http://www.chinaxiv.org/abs/202003.00026) medRxiv (https://doi.org/10.1101/2020.04.20.20061861) medRxiv (https://doi.org/10.1101/2020.04.23.20076612) Assistance Publique Hopitaux De Paris (https://www.aphp.fr/contenu/le-tocilizumab-ameliore-significativement-le-pronostic-des-patients-avec-pneumonie-covid) PNAS (https://www.pnas.org/content/early/2020/04/27/2005615117#T1) medRxiv (https://doi.org/10.1101/2020.05.01.20078360) medRxiv (https://doi.org/10.1101/2020.05.07.20094599) medRxiv (https://doi.org/10.1101/2020.05.14.20099234) medRxiv (https://doi.org/10.1101/2020.05.13.20100404) medRxiv (https://doi.org/10.1101/2020.05.13.20100081) | FDA-approved since 2010, approved to treat various type of arthritis, including rheumatoid arthritis, and cytokine release syndrome | Sources | 5/21/2020 | |
20 | Treatment | Antibodies | Gimsilumab, anti-granulocyte-macrophage colony stimulating factor monoclonal | Clinical | Phase 2 study started in April 2020 | NCT04351243 | Roivant Sciences | N/A | Sources | 5/14/2020 | |||
21 | Treatment | Antibodies | TJM2 (TJ003234), anti-granulocyte-macrophage colony stimulating factor antibody | Clinical | Phase 1/2 recruiting April 2020 | NCT04341116 | I-Mab Biopharma | N/A | Sources | 4/27/2020 | |||
22 | Treatment | Antibodies | lenzilumab, anti-granulocyte-macrophage colony stimulating factor antibody | Clinical / Compassionate Use | Phase 3 not yet recruiting April 2020 | NCT04351152 | Humanigen Inc. | Prevent cytokine storm with CAR-T cancer therapy; prevention/treatment of acute graft versus host disease; chronic myelomonocytic leukemia; eosinophilic asthma | N/A | Sources | 4/27/2020 | ||
23 | Treatment | Antibodies | Sylvant (siltuximab), interleukin-6 targeted monoclonal | Clinical / Compassionate Use | Compassionate use data shared April 2020; Phase 3 recruiting April 2020 | NCT04322188 NCT04330638 NCT04329650 | EUSA Pharma/The Papa Giovanni XXII Hospital; University Hospital, Ghent; Fundacion Clinic per a la Recerca Biomédica | EUSA Pharma (https://www.eusapharma.com/news/interim-analysis-data-for-siltuximab-treated-covid-19-patients-from-the-sisco-study/) medRxiv (https://doi.org/10.1101/2020.04.01.20048561) medRxiv (https://doi.org/10.1101/2020.04.23.20076612) | FDA-approved since 2014, approved to treat multicentric Castleman disease | Sources | 4/28/2020 | ||
24 | Treatment | Antibodies | Soliris (eculizumab), complement inhibitor | Clinical/ Expanded access | Phase 2 recruiting May 2020 | NCT04288713 NCT04346797 NCT04355494 | Assistance Publique - Hopitaux de Paris (Phase 2); Alexion (Expanded Access) | FDA-approved since 2007, approved to treat Paroxysmal Nocturnal Hemoglobinuria, Atypical Hemolytic Uremic Syndrome, Generalized Myasthenia Gravis, and Neuromyelitis Optica Spectrum Disorder | Sources | 5/5/2020 | |||
25 | Treatment | Antibodies | Ilaris (canakinumab), interleukin-1beta blocker | Clinical | Novartis Phase 3 to start and trial top-line results expected late summer 2020 | NCT04348448 NCT04362813 NCT04365153 | Novartis; other research sponsors | FDA-approved since 2009, approved to treat periodic fever syndromes and systemic juvenile idiopathic arthritis | Sources | 4/30/2020 | |||
26 | Treatment | Antibodies | Gamifant (emapalumab), anti-interferon gamma antibody | Clinical | Phase 2/3 recruiting April 2020 | NCT04324021 | Swedish Orphan Biovitrum | FDA-approved since 2018, approved to treat primary hemophagocytic lymphohistiocytosis | Sources | 4/27/2020 | |||
27 | Treatment | Antibodies | meplazumab, anti-CD147 antibody | Clinical | Phase 1/2 recruiting April 2020 | NCT04275245 | Tang-Du Hospital | medRxiv (https://doi.org/10.1101/2020.03.21.20040691) | N/A | Sources | 4/27/2020 | ||
28 | Treatment | Antibodies | LY3127804, anti-Angiopoietin 2 (Ang2) antibody | Clinical | Phase 2 to start in April 2020 | Eli Lilly | N/A | Sources | Prior to 4/20/2020 | ||||
29 | Treatment | Antibodies | Ultomiris (ravulizumab-cwvz), complement inhibitor | Clinical | Phase 3 to start in May 2020 | NCT04369469 | Alexion Pharmaceuticals | FDA-approved since 2018, aprpoved to treat paroxysmal nocturnal hemoglobinuria and atypical hemolytic uremic syndrome | Sources | 5/5/2020 | |||
30 | Treatment | Antibodies | IFX-1, anti-C5a antibody | Clinical | Phase 2/3 recruiting in April 2020 | NCT04333420 | InflaRx N.V. | To treat various inflammatory conditions including hidradenitis suppurativa, ANCA-associated vasculitis, and pyoderma gangraenosum | N/A | Sources | 4/27/2020 | ||
31 | Treatment | Antibodies | otilimab, anti-granulocyte macrophase colony-stimulating factor (GM-CSF) antibody | Clinical | Phase 2 to start end of May 2020 | NCT04376684 | GSK | To treat rheumatoid arthritis | N/A | Sources | 5/8/2020 | ||
32 | Treatment | Antibodies | Monoclonal antibody cocktail | Pre-clinical | ImmunoPrecise Antibodies | N/A | Sources | 4/23/2020 | |||||
33 | Treatment | Antibodies | Antibody | Pre-clinical | Harbour BioMed/ Erasmus MC/ Utrecht University/ Mount Sinai Health System | N/A | Sources | 5/10/2020 | |||||
34 | Treatment | Antibodies | Antibodies targeting the S protein from convalescent serum, humanized mice, and phage display | Pre-clinical | Phase 1 trials begin in summer 2020 | AstraZeneca/ US Army Medical Research Institute of Infectious Diseases (USAMRIID)/ University of Maryland School of Medicine | N/A | Sources | Prior to 4/20/2020 | ||||
35 | Treatment | Antibodies | Antibody | Pre-clinical | Centivax (Distributed Bio) | N/A | Sources | 5/21/2020 | |||||
36 | Treatment | Antibodies | Antibodies | Pre-clinical | Chelsea and Westminster Hospital, Imperial College London | UK Government | N/A | Sources | 5/10/2020 | ||||
37 | Treatment | Antibodies | Antibody | Pre-clinical | Phase 1 trial begins in summer 2020 | Vanderbilt Vaccine Center/ AstraZeneca/ IDBiologics | Defense Advanced Research Projects Agency/ Dolly Parton | N/A | Sources | 5/10/2020 | |||
38 | Treatment | Antibodies | Antibodies | Pre-clinical | Medicago/ Laval University's Infectious Disease Research Centre | Canadian Institutes for Health Research (CIHR) | N/A | Sources | Prior to 4/20/2020 | ||||
39 | Treatment | Antibodies | Antibodies | Pre-clinical | FairJourney Biologics/ Iontas | N/A | Sources | 4/21/2020 | |||||
40 | Treatment | Antibodies | Antibodies | Pre-clinical | Prellis Biologics | N/A | Sources | 5/21/2020 | |||||
41 | Treatment | Antibodies | Antibodies (OmniChicken platform) | Pre-clinical | Ligand Pharmaceuticals | N/A | Sources | 4/23/2020 | |||||
42 | Treatment | Antibodies | Antibodies (OmniRat platform) | Pre-clinical | Ligand Pharmaceuticals | N/A | Sources | 4/23/2020 | |||||
43 | Treatment | Antibodies | Monocloncal antibodies, TLR4 antagonist | Pre-clinical | Edesa Biotech/ Light Chain Bioscience (NovImmune) | N/A | Sources | 4/23/2020 | |||||
44 | Treatment | Antibodies | Monocloncal antibodies, CXC10 antagonist | Pre-clinical | Edesa Biotech/ Light Chain Bioscience (NovImmune) | N/A | Sources | 4/23/2020 | |||||
45 | Treatment | Antibodies | Polyclonal hyperimmune globulin (H-IG) | Pre-clinical | Phase 2 trials begin ~ August 2020 | Emergent BioSolutions/ National Institute of Allergy and Infectious Diseases (NIAID) | Biomedical Advanced Research and Development Authority (BARDA) | Same human hyperimmune platform as FDA-approved anthrax treatment (Anthrasil) and smallpox vaccine complications (VIGIV) were developed | N/A | Sources | Prior to 4/20/2020 | ||
46 | Treatment | Antibodies | Horse plasma product (COVID-EIG) | Pre-clinical | Phase 2 trials begin ~ August 2020 | Emergent BioSolutions | Same equine hyperimmune platform as FDA-approved botulism anti-toxin (BAT) is produced | N/A | Sources | Prior to 4/20/2020 | |||
47 | Treatment | Antibodies | Convalescent plasma (blood plasma from recovered patients) | Clinical / Expanded Access | Phase 2 and Phase 3 trials not yet recruiting as of April 2020 | Many expanded access, observational, patient registry, plasma collection, prevention, and other studies listed in clincialtrials.gov, including: NCT04321421 NCT04292340 NCT04316728 NCT04338360 NCT04345289 NCT04349410 NCT04346589 NCT04333251 NCT04361253 NCT04323800 NCT04359810 NCT04362176 NCT04354831 NCT04360486 | Multiple global research sponsors, including New York State Department of Health, Johns Hopkins University, the Feinstein Institutes | Bloomberg Philantropies and the State of Maryland (to Johns Hopkins University)/ Biomedical Advanced Research and Development Authority (BARDA) (to Mayo Clinic) | medRxiv (https://doi.org/10.1101/2020.03.16.20036145) JAMA (https://jamanetwork.com/journals/jama/fullarticle/2763983) medRxiv (https://doi.org/10.1101/2020.04.07.20056440) JAMA Network (https://jamanetwork.com/journals/jama/fullarticle/2763982) medRxiv (https://doi.org/10.1101/2020.05.08.20095471) medRxiv (https://doi.org/10.1101/2020.05.12.20099879) | N/A | Sources | 5/20/2020 | |
48 | Treatment | Antibodies | Antibodies from recovered COVID-19 patients | Pre-clinical | Phase 1 trial begins Q3 2020 | Tsinghua University / Third People's Hospital of Shenzhen / Brii Biosciences | N/A | Sources | Prior to 4/20/2020 | ||||
49 | Treatment | Antibodies | Polyclonal hyperimmune globulin (H-IG) | Pre-clinical | Grifols | Biomedical Advanced Research and Development Authority (BARDA) | N/A | Sources | Prior to 4/20/2020 | ||||
50 | Treatment | Antibodies | Antibodies from recovered COVID-19 patients | Pre-clinical | Grifols | Biomedical Advanced Research and Development Authority (BARDA) | N/A | Sources | Prior to 4/20/2020 | ||||
51 | Treatment | Antibodies | Antibodies from recovered COVID-19 patients | Pre-clinical | Amgen / Adaptive Biotechnologies | N/A | Sources | Prior to 4/20/2020 | |||||
52 | Treatment | Antibodies | Antibodies from recovered COVID-19 patients | Pre-clinical | Innovent Biologics | N/A | Sources | Prior to 4/20/2020 | |||||
53 | Treatment | Antibodies | Antibodies from recovered COVID-19 patients | Pre-clinical | Xbiotech / BioBridge Global | N/A | Sources | Prior to 4/20/2020 | |||||
54 | Treatment | Antibodies | Antibodies from recovered COVID-19 patients | Pre-clinical | Costa Rican Social Security Fund (CCSS)/ The University of Costa Rica (UCR)/ Clodomiro Picado Institute | N/A | Sources | Prior to 4/20/2020 | |||||
55 | Treatment | Antibodies | Novel IgM and IgA antibodies | Pre-clinical | Atreca/ BeiGene/ IGM Biosciences | N/A | Sources | 5/4/2020 | |||||
56 | Treatment | Antibodies | SAB-185, Polyclonal hyperimmune globulin (H-IG) | Pre-clinical | Phase 1 starts early summer 2020 | CSL Behring/ SAb Biotherapeutics | Biomedical Advanced Research and Development Authority (BARDA)/ US Department of Defense | N/A | Sources | 4/30/2020 | |||
57 | Treatment | Antibodies | Non-viral gene therapy to produce monoclonal antibodies | Pre-clinical | Generation Bio / Vir Biotechnology | N/A | Sources | Prior to 4/20/2020 | |||||
58 | Treatment | Antibodies | rCIG (recombinant anti-coronavirus 19 hyperimmune gammaglobulin), polyclonal antibodies | Pre-clinical | GigaGen | N//A | Sources | Prior to 4/20/2020 | |||||
59 | Treatment | Antibodies | IC14, recombinant chimeric anti-CD14 monoclonal antibody | Expanded access | NCT04346277 | Implicit Bioscience | Acute Respiratory Distress Syndrome | N/A | Sources | Prior to 4/20/2020 | |||
60 | Treatment | Antibodies | MEDI3506, monoclonal antibody targeting interleukin 33 | Clinical | ACCORD Phase 2 trial to start May 2020 | AstraZeneca; ACCORD trial | UK Government (ACCORD study) | Chronic Obstructive Pulmonary Diesase | N/A | Sources | 5/10/2020 | ||
61 | Treatment | Antibodies | Octagam; intravenous Immunoglobulin (IVIG) | Clinical | Phase 3 trial to start May 2020 | NCT04261426 NCT04264858 NCT04350580 | Multiple global research sponsors; Octapharma USA/ Sharp Memorial Hospital | Open Forum Infectious Diseases (https://academic.oup.com/ofid/article/7/3/ofaa102/5810740) | FDA-approved since 2014, approved to treat chronic immune thrombocytopenic purpura (ITP) | Sources | 5/21/2020 | ||
62 | Treatment | Antibodies | Purified ovine immunoglobulin from immunized sheep | Pre-clinical | Public Health England (Stuart Dowall) | UK Government | N/A | Sources | 4/23/2020 | ||||
63 | Treatment | Antibodies | Antibodies | Pre-clinical | Ablexis/ AlivaMab Discovery Services/ Berkeley Lights Collaborate | N/A | Sources | 4/28/2020 | |||||
64 | Treatment | Antibodies | JS016 antibody candidate | Pre-clinical | Phase 1 to start 2Q 2020 | Junshi Biosciences/ Eli Lilly | N/A | Sources | 5/5/2020 | ||||
65 | Treatment | Antibodies | Linked nanobody antibody | Pre-clinical | University of Texas at Austin/ US National Institutes of Health/ Ghent University | N/A | Sources | 5/1/2020 | |||||
66 | Treatment | Antibodies | Single domain antibodies (sdAbs), engineered monoclonal antibody derived from camelids | Pre-clinical | Abcore | N/A | Sources | 5/21/2020 | |||||
67 | Treatment | Antivirals | Favilavir/Favipiravir/T-705/Avigan, licensed in Japan to treat influenza | Clinical | Phase 3 trial in Japan started in March 2020; Phase 2 trial in US started April 2020; Phase 3 trial in India started May 2020 with results expected by July/August 2020 (Glenmark) | NCT04303299 NCT04310228 ChiCTR2000029548 ChiCTR2000029496 ChiCTR2000029544 ChiCTR2000030254 NCT04336904 NCT04333589 NCT04345419 | Fujifilm Toyama Chemical/Zhejiang Hisun Pharmaceuticals/numerous trials with global research sponsors/ Brigham and Women's Hospital, Massachusetts General Hospital, and the University of Massachusetts Medical School/ Glenmark Pharmaceuticals | medRxiv (https://doi.org/10.1101/2020.03.17.20037432) medRxiv (https://doi.org/10.1101/2020.04.21.20066761) Kyodo News (https://english.kyodonews.net/news/2020/05/fce701d4d88d-antiflu-avigan-not-showing-apparent-efficacy-in-coronavirus-treatment.html) | N/A | Sources | 5/21/2020 | ||
68 | Treatment | Antivirals | Kaletra/Aluvia (lopinavir/ritonavir), HIV-1 protease inhibitor | Clinical | RECOVERY trial results expected by June 2020 | NCT04303299 NCT04255017 ChiCTR2000029548 ChiCTR2000029539 EudraCT 2020-000936-23 NCT04307693 NCT04315948 NCT04252885 NCT04276688 NCT02735707 NCT04321993 2020-001113-21 NCT04286503 NCT04328012 NCT04346147 | Global hospital testing (AbbVie); World Health Organization SOLIDARITY trial (studying lopinavir/ ritonavir with and without interferon beta); University of Oxford RECOVERY trial; REMAP-CAP global trial | UK Government (University of Oxford RECOVERY trial) | NEJM (https://www.nejm.org/doi/pdf/10.1056/NEJMoa2001282?articleTools=true) medRxiv (https://doi.org/10.1101/2020.03.19.20038984) Chinese Journal of Infectious Diseases (http://rs.yiigle.com/yufabiao/1182592.htm) medRxiv (https://doi.org/10.1101/2020.03.28.20045955) medRxiv (https://doi.org/10.1101/2020.04.08.20057539) medRxiv (https://doi.org/10.1101/2020.04.21.20066761) medRxiv (https://doi.org/10.1101/2020.04.25.20079079) medRxiv (https://doi.org/10.1101/2020.04.24.20077735) The Lancet (https://www.thelancet.com/journals/lancet/article/PIIS0140-6736(20)31042-4/fulltext) medRxiv (https://doi.org/10.1101/2020.05.13.20094193) | FDA-approved since 2000, approved to treat HIV-1 infection | Sources | 5/20/2020 | |
69 | Treatment | Antivirals | remdesivir, nucleotide analog | Clinical / Expanded Access / FDA issued an Emergency Use Authorization on May 1, 2020 | Gilead Phase 3 trial topline results released April 2020 (severe disease) and expected May 2020 (moderate disease); NIAID trial preliminary data released April 2020, full results expected in May 2020 | NCT04257656 NCT04252664 NCT04292730 NCT04292899 NCT04280705 EudraCT 2020-000936-23 NCT04315948 NCT04302766 NCT04323761 NCT04349410 | Gilead; World Health Organization SOLIDARITY trial; National Institute of Allergy and Infectious Disease (NIAID)'s Adaptive COVID-19 Treatment Trial; Feinstein Institutes | NEJM (https://www.nejm.org/doi/full/10.1056/NEJMoa2007016) NEJM (https://www.nejm.org/doi/full/10.1056/NEJMoa2001191) Stat News (https://www.statnews.com/2020/04/16/early-peek-at-data-on-gilead-coronavirus-drug-suggests-patients-are-responding-to-treatment/) Reuters (https://www.reuters.com/article/us-health-coronavirus-gilead-sciences/gilead-disputes-report-that-coronavirus-drug-trial-flopped-idUSKCN225326) Stat (https://www.statnews.com/2020/04/23/data-on-gileads-remdesivir-released-by-accident-show-no-benefit-for-coronavirus-patients/) medRxiv (https://doi.org/10.1101/2020.04.21.20066761) Gilead (https://www.businesswire.com/news/home/20200429005424/en/Gilead-Announces-Results-Phase-3-Trial-Investigational) NIAID (https://www.niaid.nih.gov/news-events/nih-clinical-trial-shows-remdesivir-accelerates-recovery-advanced-covid-19?utm_campaign=+42538088&utm_content=&utm_medium=email&utm_source=govdelivery&utm_term=) Lancet (https://doi.org/10.1016/S0140-6736(20)31022-9) medRxiv (https://doi.org/10.1101/2020.05.02.20088559) | Treatment of Ebola | N/A | Sources | 5/20/2020 | |
70 | Treatment | Antivirals | Prezcobix (darunavir, HIV-1 protease inhibitor/cobicistat, CYP3A inhibitor) | Clinical | Phase 3 trials recruiting May 2020 | ChiCTR2000029541 NCT04252274 NCT04303299 NCT04304053 | Multiple global research sponsors | FDA-approved since 2015, approved to treat HIV-1 infection | Sources | 5/20/2020 | |||
71 | Treatment | Antivirals | galidesivir | Clinical | Phase 1b recruiting May 2020 | NCT03891420 | BioCryst Pharmaceuticals | National Institute of Allergy and Infectious Diseases (NIAID) | Treatment of yellow fever | N/A | Sources | 5/7/2020 | |
72 | Treatment | Antivirals | Ganovo (danoprevir), hepatitis C virus NS3 protease inhibitor; ritonavir; interferon, approved in China to treat Hepatitis C | Clinical | Small open label trial completed and results released in March 2020; Larger open label trial recruiting May 2020 | NCT04291729 NCT04345276 | Ascletis/Chinese research sponsors | medRxiv (https://doi.org/10.1101/2020.03.22.20034041) | Treatment of Hepatitis C | N/A | Sources | 5/7/2020 | |
73 | Treatment | Antivirals | ASC09, HIV protease inhibitor | Clinical | Phase 3 trial recruiting May 2020 | NCT04261907 NCT04261270 | Ascletis/Chinese research sponsors | Treatment of HIV/AIDS | N/A | Sources | 5/7/2020 | ||
74 | Treatment | Antivirals | Truvada (emtricitabine and tenofovir, both HIV-1 nucleoside analog reverse transcriptase inhibitors) | Clinical | Phase 3 trial recruiting May 2020 | ChiCTR2000029468 NCT04334928 | Plan Nacional sobre el Sida | FDA-approved since 2004, approved to treat and prevent HIV-1 infection | Sources | 5/7/2020 | |||
75 | Treatment | Antivirals | Arbidol (umifenovir), licensed in Russia and China for treatment of respiratory viral infections | Clinical | Phase 4 trials recruiting May 2020 | NCT04252885 NCT04350684 NCT04286503 NCT04260594 NCT04273763 | Multiple global research sponsors | medRxiv (https://doi.org/10.1101/2020.03.19.20038984) Chinese Journal of Infectious Diseases (http://rs.yiigle.com/yufabiao/1182592.htm) medRxiv (https://doi.org/10.1101/2020.03.17.20037432) medRxiv (https://doi.org/10.1101/2020.03.28.20045955) medRxiv (https://doi.org/10.1101/2020.04.08.20057539) medRxiv (https://doi.org/10.1101/2020.04.06.20042580) medRxiv (https://doi.org/10.1101/2020.04.11.20056523) medRxiv (https://doi.org/10.1101/2020.04.25.20079079) | N/A | Sources | 5/7/2020 | ||
76 | Treatment | Antivirals | Vicromax, broad spectrum antiviral | Pre-clinical | ViralClear Pharmaceuticals | Sources | Prior to 4/20/2020 | ||||||
77 | Treatment | Antivirals | ISR-50 | Pre-clinical | ISR Immune System Regulation | N/A | Sources | Prior to 4/20/2020 | |||||
78 | Treatment | Antivirals | Tamiflu (oseltamivir), neuraminidase inhibitor | Clinical | REMAP-CAP trial recruiting May 2020 | NCT04303299 NCT04255017 NCT04261270 NCT02735707 NCT04338698 NCT04371601 | Roche; REMAP-CAP global trial | medRxiv (https://doi.org/10.1101/2020.03.28.20045955) medRxiv (https://doi.org/10.1101/2020.04.11.20056523) | FDA-approved since 1999, approved to treat and prevent influenza | Sources | 5/7/2020 | ||
79 | Treatment | Antivirals | antiviral Fc conjugates | Pre-clinical | Cidara Therapeutics | N/A | Sources | Prior to 4/20/2020 | |||||
80 | Treatment | Antivirals | Antiviral compounds | Pre-clinical | Cocrystal Pharma | N/A | Sources | Prior to 4/20/2020 | |||||
81 | Treatment | Antivirals | EIDD-2801, oral ribonucleoside analog | Clinical | Phase 1 started April 2020 | Ridgeback Biotherapeutics / Drug Innovation Ventures at Emory (DRIVE) | N/A | Sources | Prior to 4/20/2020 | ||||
82 | Treatment | Antivirals | Virazole (ribavirin for inhalation solution) | Clinical / Compassionate Use | Phase 1 recruiting May 2020 | NCT04356677 | Bausch Health | FDA-approved since 1985, approved to treat lower respiratory tract infections due to RSV | Sources | 5/7/2020 | |||
83 | Treatment | Antivirals | Antiviral drug combinations | Pre-clinical | SCORE consortium (universities of Aix-Marseille, Leuven, Utrecht, Bern, and Lubeck), the Helmholtz Centre for Infection Research, and Janssen Pharmaceutica NV | EU Commission (Horizon 2020 Program) | Unknown | Sources | Prior to 4/20/2020 | ||||
84 | Treatment | Antivirals | Levovir (clevudine) | Clinical | Phase 2 trial not yet recruiting | NCT04347915 | Bukwang Pharm | Sources | 5/7/2020 | ||||
85 | Treatment | Antivirals | AB001 | Pre-clinical | Phase 1 to start in 2020 | Agastiya Biotech | N/A | Sources | 4/24/2020 | ||||
86 | Treatment | Antivirals | BTL-tml | Clinical | Has been used in 36 patients anecdotally | Beech Tree Labs | Treatment of herpes virus infections | N/A | Sources | 5/5/2020 | |||
87 | Treatment | Antivirals | DAS181, recombinant sialidase (nebulized) | Compassionate Use/ Clinical | Compassionate use finding released in May 2020; Phase 2/3 started enrolling in May 2020 | NCT03808922 NCT04354389 NCT04298060 NCT04324489 | Ansun Biopharma/ Renmin Hospital of Wuhan University | PR Newswire (https://www.prnewswire.com/news-releases/ansun-biopharma-announces-positive-results-from-investigator-initiated-trial-of-novel-covid-19-treatment-301033871.html) | Treatment of lower respiratory tract parainfluenza virus infections and severe influenza infections | N/A | Sources | 5/5/2020 | |
88 | Treatment | Antivirals | emetine hydrochloride | Clinical | Phase 2/3 to start in Q3 2020 | Acer Therapeutics/ US National Center for Advancing Translational Sciences (NCATS) | To treat viral hepatitis and varicella-virus | N/A | Sources | 5/13/2020 | |||
89 | Treatment | Antivirals | AT-527, oral purine nucleotide prodrug | Clinical | Phase 2 trial to start May 2020 | NCT04396106 | Atea Pharmaceuticals | Treatment of Hepatitis C infections | N/A | Sources | 5/21/2020 | ||
90 | Treatment | Cell-based therapies | PLX cell product, placenta-based cell therapy | Clinical/ Compassionate Use | Results from compassionate use released in April 2020 | Pluristem Therapeutics/BIH Center for Regenerative Therapy/Berlin Center for Advanced Therapies | Pluristem Therapeutics (https://www.pluristem.com/wp-content/uploads/2020/04/PSTI-PR-Follow-up-on-Covid-19-treatments-FINAL-FOR-RELEASE.pdf) | Various conditions | N/A | Sources | 5/8/2020 | ||
91 | Treatment | Cell-based therapies | Mesenchymal stem cells | Clinical | Phase 1 trials ongoing May 2020; Phase 1/2 trials recruiting May 2020; Phase 2/3 trial recruiting May 2020 | 30 trials listed in clinicaltrials.gov ChiCTR2000029990 NCT04315987 NCT04302519 NCT04288102 NCT04313322 NCT04273646 NCT04371601 NCT04315987 NCT04252118 NCT04336254 NCT04339660 NCT04371601 NCT04366063 | Numerous trials with global research sponsors | Aging and Disease (http://www.aginganddisease.org/article/0000/2152-5250/ad-0-0-216.shtml) ChinaXiv (http://chinaxiv.org/abs/202002.00084) | N/A | Sources | 5/8/2020 | ||
92 | Treatment | Cell-based therapies | Autologous Adipose-Tissue Derived Mesenchymal Stem Cells (ADMSCs) | Expanded access | Celltex | Celltex (https://celltexbank.com/transplantation-of-ace2-mesenchymal-stem-cells-improves-the-outcome-of-patients-with-covid-19-pneumonia/) Celltex (https://celltexbank.com/chinaxiv-reports-clinical-remission-of-a-critically-ill-covid-19-patient-treated-by-human-umbilical-cord-mesenchymal-stem-cells/) | Injuries, Pain, and Autoimmune, Vascular and Other Disease, including Inflammatory lung conditions, pneumonia, and chronic obstructive pulmonary disease (COPD) | N/A | Sources | 5/13/2020 | |||
93 | Treatment | Cell-based therapies | Ryoncil (remestemcel-L), allogenic mesenchymal stem cells | Clinical/ Compassionate Use/ Expanded Access | Compassionate use data shared April 2020; Phase 3 trial recruiting May 2020 | NCT04366830 NCT04371393 | Mesoblast/ Cardiothoracic Surgical Trials Network | Mesoblast (http://investorsmedia.mesoblast.com/static-files/337e723a-340d-493e-a4a1-0971d2c71460) | Graft versus host disease and other rare diseases, chronic obstructive pulmonary disease | N/A | Sources | 5/7/2020 | |
94 | Treatment | Cell-based therapies | MultiStem, bone marrow stem cells | Clinical | Phase 2/3 trial recruiting May 2020 | NCT04367077 | Athersys / The University of Texas Health Science Center at Houston | Medical Technology Enterprise Consortium (MTEC) | Acute Respiratory Distress Syndrome; Stroke | Sources | 5/10/2020 | ||
95 | Treatment | Cell-based therapies | Allogeneic T-cell therapies | Pre-clinical | AlloVir/Baylor College of Medicine | N/A | Sources | Prior to 4/20/2020 | |||||
96 | Treatment | Cell-based therapies | Natural killer cell-based therapy | Pre-clinical | Begin Phase 1 by end of 2020 | GC LabCell / KLEO Pharmaceuticals | N/A | Sources | Prior to 4/20/2020 | ||||
97 | Treatment | Cell-based therapies | CYNK-001, allogeneic, natural killer cell therapy | Clinical | Phase 1/2 study not yet recruiting May 2020 | NCT04365101 | Celularity/ Lung Biotechnology PBC | Various hematologic cancers and solid tumors | N/A | Sources | 5/7/2020 | ||
98 | Treatment | Cell-based therapies | CAP-1002, allogenic cardiosphere-derived cells | Expanded access | Expanded access trial ongoing May 2020 | NCT04338347 | Capricor Inc. | Duchenne muscular dystrophy | N/A | Sources | 5/7/2020 | ||
99 | Treatment | Cell-based therapies | haNK, natural killer cells | Clinical | ImmunityBio / NantKwest | N/A | Sources | 5/21/2020 | |||||
100 | Treatment | Cell-based therapies | Bone marrow-derived allogenic mesenchymal stem cells (BM-Allo-MSC) | Pre-clinical | Phase 1b trial to start in Q2 2020 | ImmunityBio/ NantKwest/ Be The Match BioTherapies | N/A | Sources | 5/21/2020 | ||||
101 | Treatment | Cell-based therapies | Allogenic, adipose-derived mesenchymal stem cells (HB-adMSCs) | Clinical | Phase 2 started in April 2020 | NCT04348435 NCT04349631 NCT04362189 | Hope Biosciences | Hope Biosciences Stem Cell Research Foundation | Rheumatoid arthritis | N/A | Sources | 4/24/2020 |