Clinical benefit of remdesivir in rhesus macaques infected with SARS

Aug 11, 2023

Nature volume 585, pages 273–276 (2020)Cite this article

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Effective therapies to treat coronavirus disease 2019 (COVID-19) are urgently needed. While many investigational, approved, and repurposed drugs have been suggested as potential treatments, preclinical data from animal models can guide the search for effective treatments by ruling out those that lack efficacy in vivo. Remdesivir (GS-5734) is a nucleotide analogue prodrug with broad antiviral activity1,2 that is currently being investigated in COVID-19 clinical trials and recently received Emergency Use Authorization from the US Food and Drug Administration3,4. In animal models, remdesivir was effective against infection with Middle East respiratory syndrome coronavirus (MERS-CoV) and severe acute respiratory syndrome coronavirus (SARS-CoV)2,5,6. In vitro, remdesivir inhibited replication of SARS-CoV-27,8. Here we investigate the efficacy of remdesivir in a rhesus macaque model of SARS-CoV-2 infection9. Unlike vehicle-treated animals, macaques treated with remdesivir did not show signs of respiratory disease; they also showed reduced pulmonary infiltrates on radiographs and reduced virus titres in bronchoalveolar lavages twelve hours after the first dose. Virus shedding from the upper respiratory tract was not reduced by remdesivir treatment. At necropsy, remdesivir-treated animals had lower lung viral loads and reduced lung damage. Thus, treatment with remdesivir initiated early during infection had a clinical benefit in rhesus macaques infected with SARS-CoV-2. Although the rhesus macaque model does not represent the severe disease observed in some patients with COVID-19, our data support the early initiation of remdesivir treatment in patients with COVID-19 to prevent progression to pneumonia.

We have recently established a rhesus macaque model of SARS-CoV-2 infection9. In this model, infected rhesus macaques develop mild to moderate, transient respiratory disease, with pulmonary infiltrates visible on radiographs and a shedding pattern similar to that observed in patients with COVID-19. The observed clinical signs and high viral loads enable the testing of the treatment efficacy of direct-acting antivirals in this model.

Two groups of six rhesus macaques were inoculated with SARS-CoV-2 strain nCoV-WA1-2020. Twelve hours after inoculation, one group was given 10 mg kg−1 intravenous remdesivir and the other group was treated with an equal volume of vehicle solution (2 ml kg−1). Treatment was continued 12 h after the first treatment and every 24 h thereafter with a dose of 5 mg kg−1 remdesivir or an equal volume of vehicle solution (1 ml kg−1). The concentration of remdesivir was determined in serum collected 12 h after the initial treatment and 24 h after subsequent doses (immediately before the next dose of treatment was administered). Remdesivir (prodrug GS-5734), its downstream alanine metabolite (GS-704277) and the parent nucleoside (GS-441524) were detected in serum from all remdesivir-treated animals (Extended Data Fig. 1a). Serum levels of the prodrug and downstream metabolites were consistent with previously published plasma levels of these compounds in healthy rhesus macaques, which showed a short systemic half-life for GS-5734 (0.39 h) resulting in transient conversion to the intermediate GS-704277 and persistence of the downstream GS-441524 product at higher plasma levels10.

Concentrations of the metabolite GS-441524 were measured in lung tissue collected from each lung lobe seven days post-inoculation (dpi) and 24 h after the last dose of remdesivir was administered; the metabolite was readily detectable in all remdesivir-treated animals. GS-441524 was generally distributed throughout all six lobes of the lung (Extended Data Fig. 1b). GS-704277 was not detected in lung tissue. Although the pharmacologically active metabolite of remdesivir is the triphosphate of GS-441524, lung homogenate samples spiked with the triphosphate metabolite demonstrated rapid decay of the metabolite in this matrix (data not shown). GS-441524 levels were taken as a surrogate for tissue loading and suggest that the current dosing strategy delivered drug metabolites to the sites of SARS-CoV-2 replication in infected animals.

After inoculation with SARS-CoV-2, the animals were assigned a daily clinical score based on a pre-established scoring sheet in a blinded fashion. Twelve hours after the first administration of remdesivir, clinical scores in remdesivir-treated animals were significantly lower than in control animals receiving vehicle solution. This difference in clinical score was maintained throughout the study (Fig. 1a). Only one of the six remdesivir-treated animals showed mild dyspnea, whereas tachypnea and dyspnea were observed in all vehicle-treated controls (Extended Data Table 1). Radiographic pulmonary infiltrates are one of the hallmarks of COVID-19 in humans. Radiographs taken on 0, 1, 3, 5, and 7 dpi showed significantly less lung lobe involvement and less severe pulmonary infiltration in animals treated with remdesivir than in those treated with vehicle (Fig. 1b, c).

a, Daily clinical scores for animals infected with SARS-CoV-2 and treated with remdesivir (red circles, n = 6) or vehicle solution (black squares, n = 6). b, Cumulative radiograph scores. Ventrodorsal and lateral radiographs were scored for the presence of pulmonary infiltrates by a clinical veterinarian according to a standard scoring system (0, normal; 1, mild interstitial pulmonary infiltrates; 2, moderate pulmonary infiltrates perhaps with partial cardiac border effacement and small areas of pulmonary consolidation; 3, severe interstitial infiltrates, large areas of pulmonary consolidation, alveolar patterns and air bronchograms). Individual lobes were scored and scores per animal per day were totalled and displayed. c, Ventrodorsal radiographs for each animal taken on 7 dpi. Areas of pulmonary infiltration are circled. Statistical analysis was performed using a two-way ANOVA with Sidak's multiple comparisons test.

On 1, 3 and 7 dpi, bronchoalveolar lavage (BAL) was performed as an indicator of virus replication in the lower respiratory tract. Although viral loads in BAL were reduced in animals treated with remdesivir, this difference was not statistically significant (Fig. 2a). However, 12 h after the first remdesivir treatment was administered, the infectious virus titre in BAL was about 100-fold lower in remdesivir-treated animals than in controls. By 3 dpi, infectious virus could no longer be detected in BAL from remdesivir-treated animals, whereas virus was still detected in BAL from four out of six control animals (Fig. 2b). Despite this reduction in virus replication in the lower respiratory tract, there was no reduction in viral load or infectious virus titre in nose, throat or rectal swabs collected from remdesivir-treated animals, except for a significant difference in virus titre in throat swabs collected on 1 dpi and in viral loads in throat swabs collected on 4 dpi (Extended Data Fig. 2).

a, b, Viral loads (a) and infectious virus titres in BAL (b) collected from rhesus macaques infected with SARS-CoV-2 and treated with remdesivir (n = 6) or vehicle solution (n = 6). TCID50, 50% tissue culture infectious dose. Statistical analysis was performed using a two-way ANOVA with Sidak's multiple comparisons test. c, Viral loads in tissues collected from all six lung lobes at necropsy on 7 dpi from rhesus macaques infected with SARS-CoV-2 and treated with remdesivir (n = 6) or vehicle solution (n = 6). Statistical analysis was performed using an unpaired t-test. Centre bars, median.

All animals were euthanized on 7 dpi. Tissue samples were collected from each lung lobe to compare virus replication between remdesivir-treated and vehicle-treated animals. In 10 out of 36 lung lobe samples collected from remdesivir-treated animals, viral RNA could not be detected, whereas this was the case in only 3 out of 36 lung lobes collected from control animals. In general, comparison across individual lung lobes in the two groups showed a lower geometric mean of viral RNA in the remdesivir-treated group (Extended Data Fig. 3a). Together, these data show that the viral load was significantly lower in lungs from remdesivir-treated animals than in those from vehicle-treated controls (Fig. 2c). Virus could be isolated from lung lobes of five out of six vehicle-treated control animals, but not from any of the lung tissue collected from remdesivir-treated animals. Although quantitative PCR with reverse transcription (qRT–PCR) showed that fewer tissues from other positions in the respiratory tract were positive for viral RNA in remdesivir-treated animals than in controls, these differences were not statistically significant (Extended Data Fig. 3b).

At necropsy on 7 dpi, lungs were assessed grossly for lesions. Gross lung lesions were observed in one out of six remdesivir-treated animals. By contrast, all six vehicle-treated control animals had visible lesions, resulting in a statistically significant difference in the area of the lungs affected by lesions (Fig. 3a, b, Extended Data Fig. 4a, b). This difference was also evident when calculating the lung weight-to-bodyweight ratio as an indicator of pneumonia; this ratio was significantly lower in remdesivir-treated than in vehicle-treated animals (Extended Data Fig. 4c). Histologically, remdesivir-treated animals had fewer and less severe lesions than did vehicle-treated controls. Histological lung lesions were absent in three out of six remdesivir-treated animals; the three remaining animals developed minimal pulmonary pathology. Lesions in these animals were characterized as widely separated, minimal, interstitial pneumonia frequently located in subpleural spaces (Fig. 3c, e). Five out six vehicle-treated animals developed multifocal, mild-to-moderate, interstitial pneumonia (Fig. 3d, f). We detected viral antigen in small numbers of type I and type II pneumocytes and alveolar macrophages in all animals, regardless of treatment (Fig. 3g, h).

Rhesus macaques infected with SARS-CoV-2 and treated with remdesivir (left, n = 6) or vehicle solution (right, n = 6) were euthanized on 7 dpi. a, b, Representative dorsal views of lungs from a remdesivir-treated animal (a) and a vehicle-treated animal with focally extensive areas of consolidation (b, circles). Histological analysis was performed on three sections from six lung lobes from each of the six animals per treatment group and representative images were chosen for c–h. c, Minimal subpleural interstitial pneumonia (box) observed in three out of six remdesivir-treated animals. d, Moderate subpleural interstitial pneumonia with oedema (box) observed in five of six vehicle-treated animals. e, Boxed area from c with alveoli lined by type II pneumocytes (arrow) and alveolar spaces containing foamy macrophages (arrowhead). f, Boxed area from d with pulmonary interstitium expanded by oedema and moderate numbers of macrophages and neutrophils. Alveoli are lined by type II pneumocytes (arrows). Alveolar spaces are filled with oedema (asterisk) and small numbers of pulmonary macrophages (arrowhead). g, Viral antigen in type I pneumocytes (arrow) and type II pneumocytes (arrowhead) of a remdesivir-treated animal. h, Viral antigen in type I pneumocytes (arrow) and macrophage (arrowhead) of a vehicle-treated animal. Scale bars: c, d, 200 μm; e–h, 20 μm.

We successfully carried out deep sequencing on samples from all remdesivir-treated animals and vehicle-treated controls. Known mutations in the RNA-dependent RNA polymerase that confer resistance to remdesivir in coronaviruses11 were not detected in any of the samples tested (Supplementary Table 1).

Remdesivir is, to our knowledge, the first antiviral treatment to show proven efficacy against SARS-CoV-2 in an animal model of COVID-19. Treatment of rhesus macaques infected with SARS-CoV-2 with remdesivir reduced clinical disease and damage to the lungs. The remdesivir dosing used in rhesus macaques is equivalent to that used in humans; however, owing to the acute nature of the disease in rhesus macaques, it is hard to directly translate the timing of treatment used to corresponding disease stages in humans. In our study, treatment was administered close to the peak of virus replication in the lungs as indicated by viral loads in bronchoalveolar lavages and the first effects of treatment on clinical signs and virus replication were observed within 12 h. The efficacy of direct-acting antivirals against acute viral respiratory tract infections typically decreases with delays in treatment initation12. Thus, remdesivir treatment should be initiated as early as possible in patients with COVID-19 to achieve the maximum treatment effect.

Despite the lack of obvious respiratory signs and reduced virus replication in the lungs of remdesivir-treated animals, there was no reduction in virus shedding. This finding is very important for patient management, where a clinical improvement should not be interpreted as a lack of infectiousness. Although we have shown that remdesivir metabolites are found in the lower respiratory tract, drug levels in the upper respiratory tract have not been characterized and novel formulations with alternative routes of drug delivery should be considered to improve distribution to the upper respiratory tract, thereby reducing shedding and the potential transmission risk. However, as severe COVID-19 disease results from virus infection of the lungs, this organ is the main target of remdesivir treatment. The bioavailability and protective effect of remdesivir in the lungs of infected rhesus macaques support treatment of COVID-19 patients with remdesivir. Remdesivir treatment did not result in a clinical improvement in one clinical trial with patients with severe COVID-1913; however, another clinical trial that involved more patients showed that remdesivir treatment resulted in a shorter time to improvement than in patients who received standard care only14. Our findings in rhesus macaques indicate that remdesivir treatment should be considered as early as clinically possible to prevent progression to pneumonia in patients with COVID-19.

All animal experiments were approved by the Institutional Animal Care and Use Committee of Rocky Mountain Laboratories, NIH and carried out by certified staff in an Association for Assessment and Accreditation of Laboratory Animal Care (AAALAC) International-accredited facility, according to the institution's guidelines for animal use, following the guidelines and basic principles in the NIH Guide for the Care and Use of Laboratory Animals, the Animal Welfare Act, United States Department of Agriculture and the United States Public Health Service Policy on Humane Care and Use of Laboratory Animals. Rhesus macaques were housed in adjacent individual primate cages, allowing social interactions, in a climate-controlled room with a fixed light–dark cycle (12 h light–12 h dark). Animals were monitored at least twice daily throughout the experiment. Commercial monkey chow, treats, and fruit were provided twice daily by trained personnel. Water was available ad libitum. Environmental enrichment consisted of a variety of human interactions, manipulanda, commercial toys, videos, and music. The Institutional Biosafety Committee (IBC) approved work with infectious SARS-CoV-2 strains under BSL3 conditions. Sample inactivation was performed according to IBC-approved standard operating procedures for removal of specimens from high containment.

To evaluate the effect of remdesivir treatment on SARS-CoV-2 disease outcome, we used the recently established rhesus macaque model of SARS-CoV-2 infection that results in transient lower respiratory tract disease9. Since this is a model with little prior data, it was not possible to perform a power analysis to determine group size. The sample size was therefore based on experience with other nonhuman primate models of respiratory disease, mainly a rhesus macaque model of MERS-CoV where n = 6 yielded statistical significance. Twelve animals were randomly assigned to two groups and inoculated as described previously with a total dose of 2.6 × 106 TCID50 (50% tissue culture infectious dose) of SARS-CoV-2 strain nCoV-WA1-2020 via intranasal, oral, ocular and intratracheal routes. The efficacy of therapeutic remdesivir treatment was tested in two groups of six adult rhesus macaques (three males and three females each; 3.6–5.7 kg). Owing to the acute nature of the SARS-CoV-2 model in rhesus macaques, therapeutic treatment was initiated 12 h after inoculation with SARS-CoV-2 and continued once daily for 6 dpi. One group of rhesus macaques was treated with a loading dose of 10 mg/kg remdesivir, followed by a daily maintenance dose of 5 mg/kg. The other group of six animals served as infected controls and were administered an equal dose volume (that is, 2 ml/kg loading dose and 1 ml/kg thereafter) of vehicle solution (12% sulfobutylether-β-cyclodextrin in water and hydrochloric acid, pH 3.5) according to the same treatment schedule. This dosing scheme in rhesus macaques mimics the daily dosing tested in clinical studies involving patients with COVID-19 and results in similar systemic drug exposure. Treatment was delivered as an intravenous bolus injection (total dose delivered over approximately 5 min) administered alternatingly in the left or right cephalic or saphenous veins. Although the remdesivir treatment course used here in rhesus macaques is shorter than the standard 10-day course in patients, this shorter treatment course was chosen to enable assessment of lung pathology at a time after inoculation when pulmonary infiltrates and interstitial pneumonia would still be present. Recent data from clinical trials have shown that a 5-day treatment course has a similar clinical benefit to a 10-day treatment course in patients with COVID-1914.

The animals were observed twice daily for clinical signs of disease using a standardized scoring sheet as described previously9; the same person, who was blinded to the group assignment of the animals, assessed the animals throughout the study. The predetermined endpoint for this experiment was 7 dpi. Nose, throat and rectal swabs were collected daily during treatment administration. Clinical exams were performed on 0, 1, 3, 5, and 7 dpi on anaesthetized animals. On exam days, clinical parameters such as bodyweight, temperature, pulse oximetry, blood pressure and respiration rate were collected, as well as dorsoventral and lateral chest radiographs. Radiographs were analysed by a clinical veterinarian blinded to the group assignment of the animals. On 1, 3 and 7 dpi a BAL was performed using 10 ml sterile saline. After death on 7 dpi, necropsies were performed on the animals. The percentage of gross lung lesions were scored by a board-certified veterinary pathologist blinded to the group assignment of the animals and samples of the following tissues were collected: cervical lymph node, conjunctiva, nasal mucosa, oropharynx, tonsil, trachea, all lung lobes, mediastinal lymph node, right and left bronchus, heart, liver, spleen, kidney, stomach, duodenum, jejunum, ileum, caecum, colon, and urinary bladder. Histopathological analysis of tissue slides was performed by a board-certified veterinary pathologist blinded to the group assignment of the animals.

SARS-CoV-2 isolate nCoV-WA1-2020 (MN985325.1)15 (Vero passage 3) was kindly provided by the Centers for Disease Control (CDC) and propagated once in Vero E6 cells in Dulbecco's modified Eagle's medium (DMEM, Sigma) supplemented with 2% fetal bovine serum (Gibco), 1 mM l-glutamine (Gibco), 50 U/ml penicillin and 50 μg/ml streptomycin (Gibco) (virus isolation medium). The virus stock used was 100% identical to the initial deposited GenBank sequence (MN985325.1) and no contaminants were detected. VeroE6 cells were maintained in DMEM supplemented with 10% fetal calf serum, 1 mM l-glutamine, 50 U/ml penicillin and 50 μg/ml streptomycin.

Remdesivir (RDV; GS-5734) was manufactured at Gilead Sciences by the Department of Process Chemistry (Alberta, Canada) under Good Manufacturing Practice (GMP) conditions. Batch number 5734-BC-1P was solubilized in 12% sulfobutylether-β-cyclodextrin in water and matching vehicle solution was provided to NIH.

Tributylamine was purchased from Millipore Sigma. LC–MS grade water, acetone, methanol, isopropanol and acetic acid were purchased through Fisher Scientific. All synthetic standards for molecular analysis were provided by Gilead Sciences Inc. Serum and cleared lung homogenates were gamma-irradiated (2 MRad) to inactivate infectious virus potentially present in these samples before analysis. Samples were prepared for small molecule analysis by diluting a 50-μl aliquot of either serum or clarified lung homogenate with 950 μl of 50% acetone, 35% methanol, 15% water (v/v) on ice. Samples were incubated at room temperature for 15 min and then centrifuged at 16,000g for 5 min. The clarified supernatants (850 μl) were recovered and taken to dryness in a Savant DNA120 SpeedVac concentrator (Thermo Fisher). Samples were resuspended in 100 μl of 50% methanol, 50% water (v/v) and centrifuged as before. The supernatant was taken to a sample vial for LC–MS analysis. Samples were separated using an ion-pairing liquid chromatography strategy on a Sciex ExionLC AC system. Samples were injected onto a Waters Atlantis T3 column (100 Å, 3 μm, 3 mm × 100 mm) and eluted using a binary gradient from 5 mM tributylamine, 5 mM acetic acid in 2% isopropanol, 5% methanol, 93% water (v/v) to 100% isopropanol over 5.5 min. Analytes were measured using a Sciex 5500 QTRAP mass spectrometer in negative mode. Multiple reaction monitoring was performed using two signal pairs for each analyte and signal fidelity was confirmed by collecting triggered product ion spectra and comparing back to spectra of synthetically pure standards.

All analytes were quantified against an eight-point calibration curve of the respective synthetic standard prepared in the target matrix (that is, serum or cleared lung homogenate) and processed in the same manner as experimental samples. Limit of quantification (LOQ) was approximated at a signal to noise of 10. The LOQs for the measured molecules in each matrix were 5 nM for GS-441524 in both lung homogenate and serum, 1 nM for GS-704277 in both lung homogenate and serum and 0.08 nM for GS-5734 in serum. Instability of GS-5734 and the tri-phosphorylated nucleotide metabolite in the lung homogenate during tissue lysis prevented detection of these metabolites in the lung tissue.

RNA was extracted from swabs and BAL using the QiaAmp Viral RNA kit (Qiagen) according to the manufacturer's instructions. Tissues (30 mg) were homogenized in RLT buffer and RNA was extracted using the RNeasy kit (Qiagen) according to the manufacturer's instructions. For detection of viral RNA, 5 μl RNA was used in a one-step real-time RT–PCR E assay16 using the Rotor-Gene probe kit (Qiagen) according to the manufacturer's instructions. In each run, standard dilutions of RNA standards counted by droplet digital PCR were run in parallel, to calculate copy numbers in the samples.

Virus titrations were performed by end-point titration in Vero E6 cells. Tissue was homogenized in 1 ml DMEM using a TissueLyser (Qiagen). Cells were inoculated with tenfold serial dilutions of swab and BAL samples. Virus isolation was performed on lung tissues by homogenizing the tissue in 1 ml DMEM and inoculating Vero E6 cells in a 24-well plate with 250 μl cleared homogenate and a 1:10 dilution thereof. One hour after inoculation of cells, the inoculum was removed and replaced with 100 μl (virus titration) or 500 μl virus isolation medium. Six days after inoculation, CPE was scored and the TCID50 was calculated.

Histopathology and immunohistochemistry were performed on rhesus macaque tissues. After fixation for a minimum of 7 days in 10% neutral-buffered formalin and embedding in paraffin, tissue sections were stained with haematoxylin and eosin (H&E). To detect SARS-CoV-2 antigen, immunohistochemistry was performed using a custom-made rabbit antiserum against SARS-CoV-2 N at a 1:1,000 dilution. Stained slides were analysed by a board-certified veterinary pathologist.

Viral RNA was extracted as described above. cDNAs were prepared as described, with minor modifications17. In brief, 3–12 μl of extracted RNA was depleted of rRNA using Ribo-Zero Gold H/M/R (Illumina) and then reverse-transcribed using random hexamers and SuperScript IV (ThermoFisher Scientific). Following RNaseH treatment, second strand synthesis was performed using Klenow fragment (New England Biolabs) and resulting double-stranded cDNAs were treated with a combined mixture of RiboShredder RNase Blend (Lucigen) and RNase, DNase-free, high conc (Roche Diagnostics, Indianapolis, IN) and then purified using Ampure XP bead purification (Beckman Coulter). Kapa's HyperPlus library preparation kit (Roche Sequencing Solutions) was used to prepare sequencing libraries from the double-stranded cDNAs. To facilitate multiplexing, adaptor ligation was performed with KAPA Unique Dual-Indexed Adapters and samples were enriched for adaptor-ligated product using KAPA HiFi HotStart Ready mix and seven PCR amplification cycles, according to the manufacturer's manual. Pools consisting of eight sample libraries were used for hybrid-capture virus enrichment using myBaits Expert Virus SARS-CoV-2 panel and following the manufacturer's manual, version 4.01, with 14 cycles of post-capture PCR amplification (Arbor Biosciences). Purified, enriched libraries were quantified using Kapa Library Quantification kit (Roche Sequencing Solutions) and sequenced as 2 × 150-base pair reads on the Illumina NextSeq 550 instrument (Illumina).

Raw fastq reads were trimmed of Illumina adaptor sequences using cutadapt version 1.1218 and then trimmed and filtered for quality using the FASTX-Toolkit (Hannon Lab). Remaining reads were mapped to the SARS-CoV-2 2019-nCoV/USA-WA1/2020 genome (MN985325.1) using Bowtie2 version 2.2.919 with parameters --local --no-mixed -X 1500. PCR duplicates were removed using picard MarkDuplicates (Broad Institute) and variants were called using GATK HaplotypeCaller version 4.1.2.020 with parameter -ploidy 2. Variants were filtered for QUAL >1000 and DP >20 using bcftools.

Statistical analyses were performed using GraphPad Prism software version 8.2.1.

Further information on research design is available in the Nature Research Reporting Summary linked to this paper.

All data included in this manuscript have been deposited in Figshare (https://doi.org/10.35092/yhjc.12111570). Sequences have been deposited in NCBI under BioProject accession number PRJNA632475.

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