Therapeutic strategies for COVID-19: progress and lessons learned

Li, Guangdi; Hilgenfeld, Rolf; Whitley, Richard; De Clercq, Erik

doi:10.1038/s41573-023-00672-y

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Review Article
Published: 19 April 2023

Therapeutic strategies for COVID-19: progress and lessons learned

Nature Reviews Drug Discovery volume 22, pages 449–475 (2023)Cite this article

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Abstract

The coronavirus disease 2019 (COVID-19) pandemic has stimulated tremendous efforts to develop therapeutic strategies that target severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) and/or human proteins to control viral infection, encompassing hundreds of potential drugs and thousands of patients in clinical trials. So far, a few small-molecule antiviral drugs (nirmatrelvir–ritonavir, remdesivir and molnupiravir) and 11 monoclonal antibodies have been marketed for the treatment of COVID-19, mostly requiring administration within 10 days of symptom onset. In addition, hospitalized patients with severe or critical COVID-19 may benefit from treatment with previously approved immunomodulatory drugs, including glucocorticoids such as dexamethasone, cytokine antagonists such as tocilizumab and Janus kinase inhibitors such as baricitinib. Here, we summarize progress with COVID-19 drug discovery, based on accumulated findings since the pandemic began and a comprehensive list of clinical and preclinical inhibitors with anti-coronavirus activities. We also discuss the lessons learned from COVID-19 and other infectious diseases with regard to drug repurposing strategies, pan-coronavirus drug targets, in vitro assays and animal models, and platform trial design for the development of therapeutics to tackle COVID-19, long COVID and pathogenic coronaviruses in future outbreaks.

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Introduction

As the causative agent of coronavirus disease 2019 (COVID-19), severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) is the seventh coronavirus known to have spilled over from other hosts such as bats and rodents into humans¹. Since its discovery in December 2019 (ref. ²), SARS-CoV-2 has caused more than 6.8 million deaths worldwide (see Related links), making it one of the deadliest viruses in human history.

The impact of the COVID-19 pandemic has been reflected in the extensive efforts to develop prevention and treatment strategies. So far, these efforts have led to multiple successful vaccines in an exceptionally rapid time frame^3,4, as well as the evaluation of a wide range of potential treatments in clinical trials, a few of which have also reached the market (Table 1). Based on lessons learned from six decades of antiviral drug discovery^5,6,7,8, two types of anti-SARS-CoV-2 agent can be considered. The first type targets viral proteins (mostly viral enzymes) to block the viral life cycle, which may have high selectivity if the targets lack human homologues, but have the potential risk of drug resistance owing to emerging variants⁵. The second type targets host proteins involved in the viral life cycle (such as the receptors involved in viral entry^9,10), which may exhibit broad-spectrum antiviral activities, but with a low degree of selectivity and potentially poor safety profiles^6,7. In addition, agents that target human proteins such as immune system modulators may be important in addressing harmful host responses to viral infection, such as ‘cytokine storm’ and thrombosis¹¹.

Table 1 Therapeutic options for the management of COVID-19 and associated diseases

Full size table

Efforts to develop COVID-19 drugs have been reviewed extensively over the pandemic^{12,13,14,15,16}, although it has been difficult for such reviews to remain timely for long given the exceptional pace at which new results have been reported. Now, with accumulated evidence in the past 3 years, there is an opportunity to summarize progress broadly, consider remaining needs and challenges, and reflect on the lessons learned. Here, we provide a comprehensive overview of virus-targeted and host-targeted agents against SARS-CoV-2, based on an extensive search identifying more than 700 agents that have been reported with anti-SARS-CoV-2 activities in preclinical and/or clinical studies (Supplementary Tables 1–3). Clinical findings for immunomodulators and anticoagulants are highlighted. We also discuss overarching topics in the discovery and development of such agents, including the strengths and limitations of drug repurposing, suitable disease models and clinical trial strategies. Owing to space limitations, readers are encouraged to consult other reviews about SARS-CoV-2 vaccines^4,17, diagnostics^18,19, biology and pathogenesis^20,21, acute and post-acute syndrome^22,23, immunology and inflammation^24,25, protein structures and functions^26,27, emerging variants^28,29 and antiviral drugs against other coronaviruses^30,31.

Viral targets for antiviral agents

SARS-CoV-2 is an enveloped, positive-sense, single-stranded RNA virus from the Coronaviridae family. With a length of ~29.9 kb, the SARS-CoV-2 genome (Fig. 1) is one of the largest among RNA viruses and encodes 16 non-structural proteins (NSP1 to NSP16), four structural proteins (spike, envelope, membrane, nucleocapsid) and nine accessory proteins²⁶. The development of virus-targeted inhibitors aims to block different stages of the SARS-CoV-2 life cycle (Fig. 2), including entry (spike inhibitors), proteolytic processing (main protease inhibitors, papain-like protease inhibitors), RNA synthesis (NSP12 to NSP16 inhibitors) and assembly (nucleocapsid inhibitors). This section focuses on drug development for these viral targets at various stages of the viral life cycle (Fig. 2).

**Fig. 2: The life cycle of SARS-CoV-2 and drug targets.**

Spike

SARS-CoV-2 spike is a homotrimeric class I fusion glycoprotein on the virion surface that is indispensable for viral entry, making it an attractive antiviral target. In most cases, the spike protein is cleaved by host proteases into a receptor-binding subunit S1 and a membrane-fusion subunit S2, heavily shielded by N-linked and O-linked glycans³². After major conformational rearrangements, the receptor-binding domain (RBD) of SARS-CoV-2 spike binds to angiotensin-converting enzyme 2 (ACE2) on the cell surface with high affinity, almost 22-fold higher than that of SARS-CoV spike for ACE2 (ref. ³³). Subsequent structural transitions and proteolytic cleavages drive the postfusion conformation of a three-helix bundle that fuses the viral membrane with the host plasma membrane³⁴. Several types of agent have been developed to inhibit the spike–ACE2 interaction or membrane fusion, including neutralizing antibodies, small-molecule inhibitors and peptide inhibitors.

Anti-spike antibodies

More than 100 monoclonal antibodies (mAbs) are marketed for the treatment of human diseases, including a few for viral infections, such as palivizumab for respiratory syncytial virus and ansuvimab for Ebola virus^12,35. So far, a handful of anti-SARS-CoV-2 mAbs and mAb cocktails have been approved or granted emergency use authorization (EUA), including bebtelovimab, sotrovimab, regdanvimab, bamlanivimab plus etesevimab, cilgavimab plus tixagevimab, casirivimab plus imdevimab and amubarvimab plus romlusevimab (Table 1). Most of these mAbs and cocktails have been authorized as early treatment options to treat outpatients with mild-to-moderate COVID-19 (ref. ³⁶). With the continuing emergence of SARS-CoV-2 variants, most mAbs are no longer recommended (Box 1) and their efficacy will need to be continually assessed³⁷.

More than 300 anti-SARS-CoV-2 mAbs have been reported, including more than 20 candidates in clinical trials (Supplementary Table 2). These candidates were mostly identified through the screening of antibodies from the memory B cells of convalescent patients or humanized mice exposed to SARS-CoV-2 (Fig. 3a). Potent wild-type mAbs can be subsequently engineered with amino acid modifications in the fragment crystallizable (Fc) region to develop mAbs with a longer half-life and enhanced effector functions³⁸. Common Fc modifications include: LALA modification with L234A+L235A; YTE modification with M252Y+S254T+T256E; LS modification with M428L+N434S; TM modification with L234F+L235E+P331S; and GAALIE modification with G236A+A330L+I332E (Fig. 3b). As an example, COV2-2130 and COV2-2196 are two synergistic IgG1κ mAbs engineered with the YTE modification (for half-life extension) and the TM modification (for reduced Fc effector functions), leading to the development of cilgavimab and tixagevimab³⁹. Although all marketed anti-SARS-CoV-2 antibodies are IgG1 mAbs (Supplementary Table 2), there is also a growing interest in developing polyclonal antibodies such as SAB-185 and XAV-19, nanobodies such as VHH-E, Nb12 and XG014 and biosynthetic proteins such as ensovibep (Supplementary Table 2). Finally, as a natural source of polyclonal antibodies against SARS-CoV-2, high-titre convalescent plasma from COVID-19 survivors might provide passive immunotherapy^40,41. However, current evidence does not generally support the efficacy of convalescent plasma in the standard treatment of COVID-19 (refs. ^42,43), and its widespread use also poses major challenges, including limited supply, administrative and logistical barriers, and antibody-dependent enhancement of SARS-CoV-2 infection⁴⁴.

**Fig. 3: Development of anti-spike monoclonal antibodies.**

Anti-spike antibodies mitigate SARS-CoV-2 infection through two main mechanisms. One is pathogen neutralization, in which antibodies that bind to spike — especially to the RBD — prevent viral entry⁴⁵. RBD-binding antibodies make up ~90% of neutralizing antibody titres in COVID-19 convalescent plasma⁴⁶. The other mechanism is antibody effector functions, in which antibodies mediate the destruction of SARS-CoV-2 virions or infected cells via the opsonization pathway, complement-dependent cytotoxicity and/or antibody-dependent cellular phagocytosis and cytotoxicity⁴⁷. Antibodies developed so far predominantly target the RBD to block the spike–ACE2 interaction (Fig. 3c), except for a few agents such as COV2-3434, S3H3 and 4A8 that target epitopes outside the spike RBD (Supplementary Table 2). RBD-binding antibodies can be categorized into four classes on the basis of the epitope landscape that they target (Fig. 3d). Neutralizing antibodies from different classes that target non-overlapping epitopes could be potentially combined into cocktails with increased potency against SARS-CoV-2 variants (Fig. 3e). Antibody cocktails such as etesevimab (class 1) plus bamlanivimab (class 2) and casirivimab (class 1) plus imdevimab (class 3) have been marketed.

It remains challenging to develop broadly neutralizing antibodies against SARS-CoV-2 variants and multiple distinct sarbecoviruses for several reasons. First, the SARS-CoV-2 spike protein is highly mutable, enabling the emergence of drug-resistance mutations³⁷. Most existing anti-spike antibodies are weakly active or inactive against Omicron variants of concern such as BA.1, BA.1.1, BA.2, BA.4 and BA.5 (refs. ^48,49), the spikes of which harbour >30 amino acid substitutions, including at least 15 located in the RBD (Fig. 3e). To counteract neutralization escape, it is important to develop potent antibodies and their combinations that target highly conserved non-overlapping epitopes within or outside the spike RBD. Second, antibody-based therapies might offer clinical benefits to certain patients early in the disease or those with undetectable anti-SARS-CoV-2 antibodies⁵⁰, but benefits are probably limited for inpatients who have already mounted endogenous antibody responses⁵¹. For instance, bamlanivimab (LY-CoV555) was prematurely withdrawn from the ACTIV-3 trial (NCT04501978) owing to its limited benefits for inpatients with COVID-19. Whether antibody therapies provide benefits in treating severe COVID-19 remains under investigation. Third, serum titres of anti-SARS-CoV-2 antibodies decrease over time⁵², and RBD-targeted antibodies may protect for only a few months⁴⁶. Broadly neutralizing super-antibodies⁵³ and antibodies encoded via lipid-nanoparticle-encapsulated mRNA⁵⁴ may have the potential to provide longer-term protection against variants of concern. Lastly, the need for intravenous or intramuscular infusion of neutralizing antibodies, their strict storage and distribution requirements, and high production costs are important factors that limit the accessibility of neutralizing antibodies to patients living in resource-limited regions with poor medical facilities.

Box 1 COVID-19 treatment guidelines and resources

COVID-19 guidelines

Labelling resources and authorization of COVID-19 therapies and vaccines

Other drug-related databases and resources

Anti-spike small molecules, peptides and engineered proteins

Small molecules such as clofazimine that potentially inhibit SARS-CoV-2 spike have been investigated (Supplementary Table 1) but so far, no results from late-stage clinical trials have been reported. Potential small-molecule inhibitors of the spike–ACE2 interaction such as MU-UNMC-2, P2119, P2165, H69C2, DRI-C23041 and AB-00011778 (Supplementary Table 1) need further optimization before they could progress towards clinical trials.

Several potent anti-spike peptide inhibitors derived from the heptad repeat α-helix regions of SARS-CoV-2, severe acute respiratory syndrome coronavirus (SARS-CoV), Middle East respiratory syndrome coronavirus (MERS-CoV) and HIV-1 spikes were first reported by Jiang’s group^55,56,57,58. EK1, a 36-amino-acid pan-coronavirus fusion peptide inhibitor derived from the SARS-CoV-2 heptad repeat 2 region, is currently in phase I COVID-19 trials⁵⁹. Despite their remarkable potency and low toxicity, antiviral peptide inhibitors might be limited by low oral bioavailability, metabolic instability and short circulation time⁶⁰. Enfuvirtide, which inhibits HIV-1 entry, is the only FDA-approved antiviral peptide, but it is now rarely recommended in clinical practice⁵. Future studies need to identify peptide inhibitors with better pharmacokinetic/pharmacodynamic (PK/PD) properties and delivery approaches⁶¹.

Thermostable designed ankyrin repeat proteins (DARPins) such as ensovibep, FSR16m and FSR22 (Supplementary Table 1) target SARS-CoV-2 spike to block the spike−ACE2 interaction. The phase III ACTIV-3/TICO trial, which was terminated early, showed no clinical benefits of ensovibep (MP0420) in hospitalized patients with COVID-19 (ref. ⁶²). However, the phase II/III EMPATHY trial showed clinical benefits of ensovibep in outpatients with symptomatic COVID-19 (NCT04828161). In general, DARPins could provide antiviral options, although optimization may still be needed.

Papain-like protease (part of NSP3)

Papain-like protease (PL^pro) is a cysteine protease that cleaves not only the pp1a and pp1ab polyproteins to release viral proteins NSP1, NSP2 and NSP3 (Supplementary Fig. 1a), but also removes host ubiquitin and ubiquitin-like interferon-stimulated gene 15 (ISG15) from signalling proteins to suppress innate immune responses⁶³. The PL^pro catalytic site contains a classical catalytic triad (Cys111–His272–Asp286) that preferentially cleaves the tetrapeptide motif LXGG↓XX in adjacent viral proteins (NSP1–NSP2, NSP2–NSP3, NSP3–NSP4) and the C-terminal tails of cellular ubiquitin and ISG15 (Supplementary Fig. 1b). Nearly 15 Å away from the catalytic site, a flexible β-hairpin loop, known as blocking loop 2 (BL2), controls substrate access to the catalytic site (Supplementary Fig. 1b).

More than 30 potent PL^pro inhibitors have been reported (Supplementary Table 1). Based on their mechanisms of action, anti-PL^pro agents can be classified into three groups: class (i), covalent inhibitors that form a C–S thioether linkage with the catalytic cysteine; class (ii), non-covalent inhibitors that block the entry of PL^pro substrates into the catalytic site; and class (iii), non-covalent inhibitors that target allosteric binding pockets (Supplementary Fig. 1c). In class (i), covalent inhibitors such as VIR250 and VIR251 (ref. ⁶⁴) are peptidomimetics that mimic the tetrapeptide motif LXGG to inhibit PL^pro peptidase activity. The ‘featureless’ two glycine residues of the LXGG motif make the development of potent peptidomimetic inhibitors difficult because only peptide substrates with two glycine residues at the P1 and P2 positions can be accommodated within the substrate-binding pocket⁶⁵. In class (ii), non-covalent inhibitors such as GRL0617, F0213, acriflavine, Jun9-72-2, Rac3k and XR8-24 (Supplementary Table 1) occupy the BL2 groove to block the channel that is used by substrates to access the catalytic site⁶⁵. Most of these inhibitors seem to only inhibit SARS-CoV and SARS-CoV-2, but not MERS-CoV, because of sequence and structural dissimilarities at the BL2 groove (Supplementary Fig. 1b). An exception is F0213, which inhibits both SARS-CoV-2 and MERS-CoV PL^pro, probably by targeting a narrow substrate-binding pocket adjacent to the BL2 groove⁶⁶. In class (iii), non-covalent inhibitors such as HE9 target an allosteric pocket (30 Å away from the catalytic site) to block the binding of ISG15 and ubiquitin to PL^pro (Supplementary Fig. 1c). Zn-ejector drugs such as disulfiram block an allosteric Zn²⁺-binding pocket of PL^pro (ref. ⁶⁷). The selectivity and toxicity of allosteric PL^pro inhibitors should be evaluated extensively because Zn ejectors may interfere with Zn-containing proteins in humans, and the ISG15-binding pocket is also present in human ubiquitin-specific peptidase 18 (USP18).

PL^pro inhibition blocks viral protein maturation and restores human immune responses⁶⁸. However, the design of selective PL^pro inhibitors is challenging, partly because PL^pro is structurally similar to a large family of human deubiquitinating enzymes (DUBs) and DUB-like proteases that also recognize ubiquitin or ubiquitin-like proteins⁶⁹. DUB and DUB-like proteases are under investigation as therapeutic targets for other human diseases, but no inhibitors of these proteins have yet been approved⁷⁰. Future development may focus on non-covalent PL^pro inhibitors in class (ii) with extensive optimizations that enhance selectivity and potency, and reduce cross-reactions with homologous DUB and DUB-like proteases in humans.

Main protease (NSP5)

The SARS-CoV-2 main protease (M^pro), also known as 3C-like protease, is a cysteine protease that cleaves the pp1a and pp1ab polyproteins to release viral proteins NSP4 to NSP16 (Fig. 4a). Inhibition of M^pro-mediated proteolytic cleavage prevents the maturation of key viral enzymes such as NSP12 and NSP13, thereby blocking subsequent viral replication (Fig. 2). The SARS-CoV-2 M^pro homodimer has a strong preference for hydrolysing glutamine residues at the P1 position of the cleavage motif Gln↓(Ser/Ala/Asn) (Fig. 4a). Although there is no known host protease with a primary cleavage site identical to that of M^pro⁷¹, some human cysteine proteases (for example, cathepsins B, K, L and S) can also cleave at the C-terminal side of Gln residues⁷²; therefore, potential cross-specificity needs to be considered when developing M^pro inhibitors.

**Fig. 4: Structure of the SARS-CoV-2 main protease and its drug-binding pocket.**

Each subunit of the M^pro homodimer possesses a catalytic dyad that is formed by a nucleophilic cysteine at position 145 (Cys145) and a nearby histidine residue at position 41 (His41)^73,74. The M^pro catalytic dyad catalyses the formation of a covalent carbon–sulfur bond between the Cys145 thiolate and the main-chain carbonyl of the substrate’s P1 glutamine⁷⁵ (Fig. 4b). Similar to the structure-based rational design of HIV-1 and hepatitis C virus (HCV) protease inhibitors^5,76, various small-molecule M^pro inhibitors have been designed to maximize drug–receptor interactions, particularly via the formation of extensive interactions with backbone atoms from the S1′, S1, S2, S3 and S4 subsites of M^pro (Fig. 4b).

More than 100 M^pro inhibitors have been reported, including leading candidates such as nirmatrelvir, ensitrelvir and SIM0417 (Supplementary Table 1). M^pro inhibitors can be classified into four groups (Fig. 4c) based on their mechanisms of action: class (i), peptidomimetic inhibitors that covalently bind to the M^pro catalytic pocket; class (ii), non-peptidomimetic inhibitors that block the M^pro catalytic pocket via covalent interactions; class (iii), orthosteric inhibitors that occupy the M^pro substrate-binding pocket through non-covalent reversible interactions; and class (iv), non-covalent inhibitors that target allosteric sites, mostly to impair M^pro dimer formation.

In class (i), peptidomimetic covalent inhibitors commonly bear an electrophilic warhead such as a nitrile (for example, nirmatrelvir), a ketone (for example, PF-00835231), an α-ketoamide (for example, compound 13b-K), an aldehyde (for example, compound 18p) or a Michael acceptor (for example, compound N3) to form a covalent bond with the catalytic Cys145 of M^pro (Supplementary Table 1). Nirmatrelvir is a peptidomimetic that harbours a nitrile warhead that covalently bonds with Cys145 to achieve reversible inhibition⁷⁷ (Fig. 4c). Nirmatrelvir inhibits all seven human coronavirus (HCoV) wild types⁷⁸ and various SARS-CoV-2 variants in cell culture⁷⁹, and substantially reduces viral loads in mice and hamsters⁸⁰.

In class (ii), non-peptidomimetic covalent inhibitors such as penicillin derivatives⁸¹, ebselen derivatives⁸², ester-derived inhibitors⁸³, spirocyclic derivatives⁸⁴ and myricetin derivatives⁸⁵ have been synthesized to block the catalytic pocket of M^pro, but their leads should be further optimized to yield better specificity and fewer off-target effects⁷¹.

In class (iii), non-covalent inhibitors such as ensitrelvir, CCF0058981, 23R, ML188 and ML300 (Supplementary Table 1) have been synthesized to block the substrate-binding pocket of M^pro without the formation of new covalent bonds. Based on a virtual-screening hit from pharmacophore filters, ensitrelvir (S-217622) was optimized to occupy the S1′, S1 and S2 subsites of M^pro using hydrogen bonds, hydrophobic contacts and π–π stacking interactions⁸⁶. Ensitrelvir inhibits many SARS-CoV-2 variants (such as Omicron BA.1 and BA.2) in cell culture⁸⁶ and reduced SARS-CoV-2 titres in a phase II/III study of patients with mild-to-moderate COVID-19, mostly within 5 days of symptom onset⁸⁷. Ensitrelvir was granted emergency regulatory approval in Japan in November 2022. The phase III SCORPIO-HR trial is investigating the efficacy and safety of oral ensitrelvir in high-risk outpatients with COVID-19 (NCT05305547).

In class (iv), allosteric inhibitors such as NB1A2, colloidal bismuth subcitrate and x1187 (Supplementary Table 1) target the M^pro dimer interface to inhibit dimer formation (Fig. 4a); however, their anti-M^pro potency and selectivity require optimization.

So far, nirmatrelvir (PF-07321332) is the most successful M^pro inhibitor, with an unprecedentedly short period of 22 months (March 2020 to December 2021) between drug discovery and market authorization. This rapid programme benefited from previous work on the development of PF-00835231 in 2003 to target the substrate-binding pocket of SARS-CoV M^pro, which shares 96% amino acid sequence identity with that of SARS-CoV-2 M^pro (ref. ⁷³). PF-00835231 development was suspended because SARS-CoV had disappeared by late 2004, and many hydrogen bond donors in its structure limited oral delivery⁸⁸. In an attempt to optimize this early lead, nirmatrelvir was quickly designed by assembling five readily available building blocks⁷⁸: a nitrile as the warhead; a canonical γ-lactam in the P1 subsite; a bicyclic proline derivative in the P2 subsite, known from boceprevir (an FDA-approved HCV protease inhibitor); a tert-leucine structure in the P3 subsite, known from boceprevir and previously shown to be optimal in tetrapeptidic SARS-CoV-2 M^pro inhibitors⁸⁹; and a trifluoroacetamide group in the P4 subsite (Fig. 4d). This combination of known structural elements was probably the key to the rapid success of nirmatrelvir. Because nirmatrelvir is mainly metabolized by human liver cytochrome P450 3A4 (CYP3A4), a strong CYP3A4 inhibitor such as ritonavir (an FDA-approved HIV inhibitor with no anti-coronavirus activity) can be co-administered to reduce CYP3A4-mediated metabolic clearance, thereby boosting the therapeutic concentration of nirmatrelvir⁷⁸.

In the phase II/III EPIC-HR study, early treatment with nirmatrelvir 300 mg plus ritonavir 100 mg twice daily for 5 days reduced COVID-19-related hospitalization (nirmatrelvir–ritonavir: 0.77%, placebo: 6.31%) and 28-day all-cause mortality (nirmatrelvir–ritonavir: 0%, placebo: 1.15%) among high-risk, unvaccinated, nonhospitalized adults with mild-to-moderate COVID-19 (ref. ⁹⁰). Based on the EPIC-HR study, ritonavir-boosted nirmatrelvir (marketed as Paxlovid) received its first EUA in the USA in December 2021, followed by approval or authorization in many countries. Paxlovid is now recommended as early treatment for outpatients who have mild-to-moderate COVID-19 and are at high risk of progression to severe COVID-19 (Table 1). Nevertheless, preliminary studies indicated occasional COVID-19 rebound after Paxlovid treatment⁹¹, and naturally occurring mutations such as E166V in M^pro may confer resistance to nirmatrelvir and ensitrelvir⁹². Paxlovid is not recommended for patients with severe renal or hepatic impairment or a history of clinically significant hypersensitivity reactions, nor for patients taking contraindicated drugs that cause significant drug–drug interactions. Future studies should monitor drug-resistant mutations and drug−drug interactions (for example, with CYP3A4 inducers) that affect the potency and safety of nirmatrelvir–ritonavir.

RNA-dependent RNA polymerase (NSP12)

SARS-CoV-2 RNA-dependent RNA polymerase (RdRp), encoded by NSP12, is a highly conserved holoenzyme involved in viral RNA replication and transcription. After M^pro-mediated proteolytic processing, mature NSP12 coordinates with other non-structural proteins (NSP7 to NSP10, NSP13 to NSP16) in the viral replication–transcription complex⁹³ (Fig. 5a), which catalyses template unwinding, RNA synthesis, RNA proofreading and RNA capping²⁷. By targeting key components of the replication–transcription complex (Fig. 5b), a series of antiviral agents can be developed to block RNA synthesis (NSP12 RdRp inhibitors), template unwinding (NSP13 helicase inhibitors), RNA proofreading (NSP14 exoribonuclease inhibitors), uridine cleavage (NSP15 endoribonuclease inhibitors) and RNA capping (NSP9 inhibitors, NSP12 NiRAN inhibitors, NSP13 ATPase inhibitors, NSP14 guanine-N7-methyltransferase inhibitors and NSP16 2′-O-methyltransferase inhibitors). NSP12 inhibitors will be described in this section, while other inhibitors will be addressed later.

**Fig. 5: The SARS-CoV-2 replication–transcription complex and its drug targets.**

NSP12 is composed of an N-terminal nidovirus RdRp-associated nucleotidyltransferase domain (NiRAN) for viral RNA capping and other activities^94,95, a dynamic interface domain and a C-terminal RdRp domain for viral RNA synthesis (Fig. 6a). During viral RNA capping, the NiRAN domain acts as a guanylyltransferase that adds a guanosine 5′-triphosphate to the 5′-end of viral RNA⁹⁶ (Fig. 5b). The NiRAN active site can be blocked by nucleos(t)ide analogues such as remdesivir triphosphate⁹⁵ and bemnifosbuvir triphosphate⁹⁷ (Fig. 6b). However, it is a challenge to develop potent NiRAN inhibitors with high specificity and low toxicity because the NiRAN domain shares significant structural homology with many human kinases, such as insulin receptor kinase, spleen tyrosine kinase and O-mannose kinase⁹⁸. The SARS-CoV-2 RdRp active site is the key drug target. Similar to HIV reverse transcriptase inhibitors⁹⁹, RdRp inhibitors can be classified into nucleos(t)ide analogues (such as remdesivir, molnupiravir, favipiravir and bemnifosbuvir) and non-nucleos(t)ide analogues (such as suramin) with different mechanisms of action (Fig. 6c).

**Fig. 6: NSP12 protein structure and its drug-binding pockets.**

Remdesivir (GS-5734) was initially synthesized in 2013 in a search for a potent nucleoside inhibitor of the respiratory syncytial virus¹⁰⁰. To improve its intracellular delivery and bypass the rate-limiting first phosphorylation step, remdesivir was synthesized as a monophosphoramidate prodrug of its parent nucleoside (GS-441524)¹⁰¹ through the addition of an amino acid ester and aryloxy-substituted phosphoryl group¹⁰². This prodrug approach, called ‘ProTide’ (Fig. 6d), has been used in two FDA-approved antivirals: the HIV reverse transcriptase inhibitor tenofovir alafenamide and the HCV NS5B polymerase inhibitor sofosbuvir. After it diffuses across the cell membrane, remdesivir undergoes a series of metabolic conversions to generate the active metabolite remdesivir triphosphate¹⁰³.

During the 2014–2016 outbreak of Ebola virus, remdesivir was identified as a potent anti-Ebola inhibitor¹⁰², but its anti-Ebola use was not pursued because of limited benefits in Ebola-infected patients¹⁰⁴. Soon after the COVID-19 outbreak, its anti-SARS-CoV-2 potential was demonstrated in preclinical and clinical studies¹⁰⁵. As an analogue of ATP, remdesivir triphosphate competes with natural ATP substrates to be efficiently incorporated into nascent RNA chains, causing delayed chain termination at the post-translocation position −3 (ref. ¹⁰⁶) (Fig. 6d). This blockade is mediated by a steric clash of the 1′-cyano group of remdesivir triphosphate with the side chain of Ser-861 (Fig. 6d) near the RdRp catalytic site¹⁰⁷. The 1′-cyano group and C-linked nucleobase of remdesivir are crucial for its anti-coronavirus activity¹⁰⁷.

Remdesivir was granted an EUA for the treatment of COVID-19 under certain conditions by the FDA in May 2020, which was followed by approval or authorization in many countries. Clinical benefits of remdesivir versus placebo or standard care have been indicated by randomized trials such as ACTT-1 (NCT04280705) and PINETREE (NCT04501952), whereas an added value of remdesivir was absent in Solidarity¹⁰⁸ and DisCoVeRy¹⁰⁹. Despite such discordance affected by various factors (such as patient status, study design and treatment timing), it is generally agreed that early treatment with remdesivir reduces viral loads and improves recovery for certain patients with COVID-19, especially when administered on an outpatient basis¹¹⁰. Remdesivir is unsuitable for oral administration and lung-specific delivery because of its low oral bioavailability and low stability in human liver microsomes¹¹¹. These shortcomings might be resolved by developing oral prodrugs of the remdesivir parent such as VV116 (approved in Uzbekistan, conditionally approved in China), GS-5245 (currently in a phase III trial: NCT05603143), ODBG-P-RVn, ATV006 and GS-621763, all of which have favourable oral bioavailability, relatively simple structure and potent anti-SARS-CoV-2 activity (Supplementary Table 1). A randomized phase III trial revealed the noninferiority of oral VV116 versus nirmatrelvir–ritonavir in reducing the time to sustained clinical recovery among symptomatic inpatients with mild-to-moderate COVID-19 (ref. ¹¹²).

Molnupiravir (EIDD-2801, MK-4482) is an oral prodrug of β-d-N⁴-hydroxycytidine (EIDD-1931)¹¹³. N⁴-hydroxycytidine has long been known to have mutagenic characteristics, mainly increasing AT to GC transition errors¹¹⁴. Molnupiravir is a mutagenic ribonucleoside analogue that was originally being developed to inhibit influenza A and B viruses¹¹³. In early 2020, a repurposing screen of existing compounds led to the discovery that molnupiravir had broad-spectrum activities against SARS-CoV-2, SARS-CoV and MERS-CoV in cell culture¹¹⁵ and animal models¹¹⁶. In the phase III MOVe-OUT trial of unvaccinated outpatients with mild-to-moderate COVID-19, primary end point events (hospitalization or death by day 29) occurred among 6.8% (48/709) of molnupiravir-treated patients and 9.7% (68/699) of placebo-treated patients¹¹⁷. Molnupiravir was first approved in the UK in November 2021 and has been marketed in many countries since then. In 2022, the platform-adaptive PANORAMIC trial reported no benefit of molnupiravir plus usual care in reducing COVID-19-associated hospitalizations or deaths among high-risk vaccinated adults within 5 days of symptom onset¹¹⁸. A large-scale real-world study also showed no benefit of molnupiravir in reducing hospitalization rates among high-risk outpatients with incomplete vaccination¹¹⁹.

Molnupiravir induces a lethal accumulation of mispaired nucleobases in the viral RNA genome through a mechanism called lethal mutagenesis or error catastrophe¹²⁰ (Fig. 6e). In the first step, molnupiravir is converted into its active metabolite, β-d-N⁴-hydroxycytidine 5′-triphosphate (EIDD-2061), which can be recognized as either cytosine or uridine triphosphate owing to ambiguous base-pairing¹²¹. In the second step, its active metabolite competes with natural cytosine or uridine triphosphates to be incorporated into the viral template strand, thus increasing the frequency of G-to-A and C-to-U transition errors in the viral RNA genome¹²². However, molnupiravir-induced mutagenesis requires a comprehensive safety evaluation because mutagenic ribonucleoside analogues might also detrimentally affect cellular DNA synthesis in mammalian cells¹²³. Molnupiravir is only approved for short-term use (≤5 consecutive days) and is not recommended for pregnant women or young patients (<18 years) owing to the potential risk of fetal toxicity and bone and cartilage toxicity. Furthermore, by definition, lethal mutagenesis will increase the viral sequence diversity. It remains unclear whether molnupiravir accelerates SARS-CoV-2 evolution to escape current vaccines and antiviral treatment. There are other mutagenic nucleoside analogues such as favipiravir¹²⁴, ribavirin, pyrimidine, purine and pyrazine derivatives, the active metabolites of which also engage in erroneous hydrogen bonding and base-pairing¹²⁵. Lethal mutagens might cause fewer adverse events if their mispairing can be confined to viral RNA.

Favipiravir (T-705), approved in Japan for influenza treatment, is a purine N-nucleoside analogue precursor that exhibits broad-spectrum activities against many RNA viruses¹²⁶. Favipiravir ribonucleoside triphosphate can be incorporated into the viral RNA primer strand to inhibit SARS-CoV-2 RNA synthesis¹²⁷, but only high-dose favipiravir reduces SARS-CoV-2 viral loads in Syrian hamsters¹²⁸. In randomized, double-blinded, placebo-controlled studies, favipiravir showed no significant benefit in improving viral clearance among outpatients with mild¹²⁹, mild-to-moderate¹³⁰ or asymptomatic or uncomplicated COVID-19 (ref. ¹³¹). In the phase III JIKI trial, favipiravir plasma concentrations decreased over time and its lower-than-predicted concentrations failed to improve clinical outcomes of Ebola-infected patients with high viral loads¹³². Low plasma concentrations of favipiravir (half-life: 2–5.5 h) might be insufficient to inhibit SARS-CoV-2 in human lung cells. Despite its emergency use in several countries (including Japan, India and Russia), anti-SARS-CoV-2 use of favipiravir is currently not recommended by the WHO or the FDA (Box 1).

Bemnifosbuvir (AT-527, RO7496998), initially designed for HCV inhibition, is a prodrug of the guanosine nucleotide analogue AT-9010 that shows a dual mechanism of inhibition against SARS-CoV-2 RdRp and NiRAN⁹⁷. The efficacy and safety of oral bemnifosbuvir versus placebo among high-risk outpatients with COVID-19 are currently being evaluated in the phase III SUNRISE-3 trial (NCT05629962). Galidesivir, an adenosine C-nucleoside analogue, showed limited benefit in a phase I study of 24 inpatients with moderate-to-severe COVID-19 (NCT03891420) and has not progressed further. Of the other NSP12 inhibitors (such as 6-72-2a, 5-iodotubercidin, HeE1-2Tyr, 5-hydroxymethyltubercidin) with in vitro activity (Supplementary Table 1), some have obvious limitations that need to be addressed. For example, sangivamycin is an experimental N-nucleoside analogue that exhibits in vitro activity against many SARS-CoV-2 variants¹³³, but targets cellular proteins, including protein kinase C and histone H3-associated protein kinase¹³³. Suramin blocks the binding of viral RNA template strand within the RdRp catalytic site (Fig. 6c) and inhibits SARS-CoV-2 replication in Vero E6 cells¹³⁴. However, suramin has never been recommended for antiviral use because of its poor bioavailability and strong side effects (the negatively charged suramin binds to many human proteins with positively charged surfaces)¹³⁵.

Helicase (NSP13)

SARS-CoV-2 helicase, a member of the 1B helicase superfamily, has RNA unwinding and adenosine 5′-triphosphatase (ATPase) activities¹³⁶. The helicase structure includes an N-terminal zinc-binding domain that coordinates zinc ions; a C-terminal RNA-binding ATPase with two RecA-like domains; and stalk and 1B domains that bridge the N-terminal and C-terminal domains⁹⁴. Dynamic structures of the helical stalk and the 1B domain are unlikely to be druggable, but the RNA-binding site and the ATPase active site (Supplementary Fig. 2) have been identified as conserved drug-binding pockets¹³⁷.

A few small-molecule leads have been reported to inhibit helicase RNA unwinding (such as FPA-124 and 2-phenylquinoline derivatives) and/or ATPase activity (such as 5645-0263 and ranitidine bismuth citrate) (Supplementary Table 1). However, further optimization to address issues such as off-target toxicity and limited potency is needed, because SARS-CoV-2 and some host helicases such as human DDX helicases¹³⁸ share similar substrate-binding structures and functions, including double-stranded RNA unwinding and NTPase hydrolysis. Although no helicase inhibitor has yet entered clinical trials for COVID-19, potent helicase inhibitors have been developed for other infectious diseases¹³⁹, including amenamevir, which is approved in Japan for herpes zoster treatment, and pritelivir, which is in a phase III trial enrolling immunocompromised patients infected with aciclovir-resistant herpes simplex virus (NCT03073967).

NSP14 exoribonuclease and guanine-N7-methyltransferase

SARS-CoV-2 NSP14 has an N-terminal exoribonuclease domain and a C-terminal guanine-N7-methyltransferase domain (Supplementary Fig. 3a) that conduct viral RNA proofreading and capping, respectively^140,141. The exoribonuclease domain of NSP14 interacts with its cofactor NSP10 to act as a 3′–5′ exoribonuclease that rectifies viral RNA mispairing by removing misincorporated nucleotides or nucleotide analogues from the 3′-end of the nascent RNA strand¹⁴¹. This proofreading mechanism is indispensable for maintaining the replication fidelity of the long SARS-CoV-2 genome¹⁴². It also limits the effectiveness of nucleos(t)ide inhibitors such as ribavirin because NSP14 exoribonuclease rapidly excises ribavirin 5′-monophosphate from the viral RNA¹⁴³. NSP14 inhibitors that target the exoribonuclease active site have been identified, such as compound#79, A-2 and B-1 (Supplementary Table 1), but off-target effects of these inhibitors should be carefully evaluated because of the structural similarity between NSP14 and human DEDD exonucleases.

NSP14 guanine-N7-methyltransferase is involved in the construction of a viral RNA cap structure that prevents viral RNA degradation and the activation of antiviral immunity¹⁴⁴. It transfers a methyl group from the S-adenosyl-l-methionine (SAM) donor to the N7 position of the guanosine 5′-triphosphate of the newly synthesized viral RNA, yielding a Cap-0-RNA structure (Supplementary Fig. 3b). A sulfonamide-based bisubstrate analogue, compound 25, harbours an adenosine to block the SAM-binding pocket and a 3-cyano-4-methoxybenzenesulfonamide ring to occupy the cap-binding pocket¹⁴⁵. Other N7-methyltransferase inhibitors (such as pyridostatin, sinefungin and DS0464) also exhibit modest anti-SARS-CoV-2 activities in cell culture (Supplementary Table 1). No NSP14 inhibitor has yet entered clinical trials for COVID-19.

Endoribonuclease (NSP15)

NSP15 is a uridine-specific endoribonuclease (Supplementary Fig. 4a) that cleaves 5′-polyuridine tracts in negative-sense viral RNA (Supplementary Fig. 4b) to evade activation of host immune responses¹⁴⁶. The active site of NSP15 Mn²⁺-dependent endoribonuclease, which cleaves viral RNA substrates and produces the 2′,3′-cyclic phosphodiester and 5′-hydroxyl termini^146,147, is a potential drug-binding pocket (Supplementary Fig. 4c). Inhibitors identified so far (Supplementary Table 1), such as tipiracil¹⁴⁸, a uracil derivative approved for the treatment of colorectal cancer, have weak activities against SARS-CoV-2 (Supplementary Fig. 4d), and further optimizations are needed. In theory, NSP15 endoribonuclease can be an attractive antiviral target owing to the lack of close human homologues.

2′-O-methyltransferase (NSP16)

SARS-CoV-2 NSP16 and its activator NSP10 form a heterodimeric 2′-O-methyltransferase complex (Supplementary Fig. 5) that efficiently converts viral RNA from the Cap-0-RNA into the Cap-1-RNA configuration for evading activation of pattern recognition receptors^144,149. Despite their anti-SARS-CoV-2 activities in cell culture, S-adenosyl-l-homocysteine (SAH) and SAM derivatives such as sinefungin usually have poor membrane permeability (due to their zwitterionic nature) and high toxicity (due to human methyltransferases such as cap-specific mRNA (nucleoside-2′-O-)-methyltransferase 1 (CMTR1)), therefore limiting their clinical applications¹⁵⁰.

NSP16 has structural homology to human CMTR1, which facilitates SARS-CoV-2 RNA methylation as an alternative route¹⁵¹. An experimental adenine analogue, called 3-deazaneplanocin A, suppresses SARS-CoV-2 replication by blocking both NSP16 2′-O-methyltransferase and human CMTR1 synergistically¹⁵¹, but causes undesirable effects such as stunted growth and nephrotoxicity in rodents¹⁵². In principle, inhibition of SARS-CoV-2 RNA methylation requires concomitant targeting of both NSP16 and CMTR1 and may have a high risk of toxicity because inhibition of human SAM cycle-related enzymes will damage human mRNA maturation¹⁵¹.

Nucleocapsid

The SARS-CoV-2 nucleocapsid is a flexible and multivalent protein (Supplementary Fig. 6) with multiple functions including viral genome packaging¹⁵³ and suppression of innate antiviral immunity¹⁵⁴. However, it remains a challenge to develop nucleocapsid inhibitors. First, drug-binding pockets in nucleocapsid, unlike those of viral proteases and RdRp, seem to be structurally dynamic¹⁵³, thereby making it difficult for stable drug binding. Second, the nucleocapsid is the most abundant SARS-CoV-2 protein and folds into the intricate ribonucleoprotein complex with viral RNA. Third, current nucleocapsid inhibitors are inferior to protease and RdRp inhibitors regarding antiviral potency and binding affinity. Despite active research in the past 30 years, no antiviral nucleocapsid inhibitor has been approved.

Other viral targets

Non-structural proteins such as NPS1, NSP6, NPS7 and NSP9 have also been explored as antiviral targets (Supplementary Table 1). Nevertheless, the specificity and potency of their potential inhibitors, mostly obtained from drug repurposing, requires further improvement and evaluation. SARS-CoV-2 accessory proteins (such as open reading frame 3a (ORF3a), ORF6 and ORF9b) are involved in a wide variety of functions, including viral replication, immune evasion, autophagy and/or apoptosis¹⁵⁵. Although a few compounds have been screened for inhibition of SARS-CoV-2 accessory proteins (Supplementary Table 1), such proteins are generally dispensable for the viral life cycle¹⁵⁶.

SARS-CoV-2 RNA structures at the conserved region are potential targets for the development of nucleic acid therapeutics (Supplementary Table 1) such as antisense oligonucleotides (for example, ASO4 (ref. ¹⁵⁷)) and small interfering RNAs (for example, O3 (ref. ¹⁵⁸) and C6G25S¹⁵⁹). However, their widespread application faces challenges such as manufacturing¹⁶⁰. No RNA-based inhibitor has yet reached COVID-19 trials.

Host targets for antiviral agents

SARS-CoV-2 hijacks host factors (n > 300) to complete its viral life cycle¹⁰, including key cellular proteins such as ACE2. Despite their limitations concerning drug selectivity and safety, antiviral agents that target conserved human proteins have the potential advantage of broad-spectrum activities against emerging variants and multiple viruses^6,9. A successful example is ibalizumab, an FDA-approved mAb that binds to the T cell surface glycoprotein CD4 to inhibit viral entry of HIV-1 and HIV-2 multidrug-resistant strains¹⁶¹. This section introduces important host proteins that have been explored as antiviral targets to interrupt the viral entry or replication of SARS-CoV-2 (Fig. 2).

Angiotensin-converting enzyme 2 (ACE2)

ACE2 is the primary entry receptor (Fig. 7a) for some human coronaviruses such as SARS-CoV-2, SARS-CoV and HCoV-NL63 (ref. ¹⁶²). At the initial stage of viral entry into host cells, the N-terminal domain of the ACE2 dimer¹⁶³ on the cell surface is recognized by the spike RBD (Fig. 7b). SARS-CoV-2 infection subsequently decreases ACE2 expression and weakens ACE2-mediated regulation of the human renin–angiotensin system, resulting in pulmonary hypertension, inflammation and cardiovascular complications¹⁶⁴.

One potential therapeutic strategy aims to block SARS-CoV-2 entry into host cells by mimicking ACE2 with peptide fragments¹⁶⁵ or mini-proteins such as APN01, a soluble extracellular fragment of wild-type human ACE2 (ref. ¹⁶⁶). However, compared with placebo control, APN01 offered no significant benefit in 28-day all-cause mortality or any use of invasive mechanical ventilation in a phase II trial involving inpatients with COVID-19 (NCT04335136). Small molecules such as SB27041 that target ACE2 have also been investigated as potential anti-SARS-CoV-2 agents in preclinical studies (Supplementary Table 3). SB27041 targets the allosteric binding pocket of ACE2 and possibly induces conformational changes to block interactions between ACE2 and SARS-CoV-2 spike without affecting ACE2 enzymatic functions¹⁶⁷.

Cellular proteases

Cellular proteases, such as furin, transmembrane protease serine 2 (TMPRSS2), cathepsin proteases, ADAM10 and ADAM17, cleave and prime SARS-CoV-2 spike for viral entry^168,169,170. Membrane fusion of SARS-CoV-2 virions into host cells depends on proteolytic cleavage of viral spike via a two-step process (Fig. 7a): first, furin-mediated cleavage at the S1/S2 site (⁶⁸⁴AR↓SV⁶⁸⁷) to release the receptor-binding subunit S1 and the membrane-fusion subunit S2 (ref. ¹⁷¹); and second, proteolytic cleavage at the S2′ site (⁸¹⁴KR↓SF⁸¹⁷), located within the membrane-fusion subunit S2, to release the fusion peptide of spike that anchors the host cell membrane¹⁷². Cleavage at the S2′ site is processed by TMPRSS2 or TMPRSS13 during rapid cell–membrane fusion¹⁷³ or endosomal cathepsin proteases (primarily cathepsin B and L) during slow endosomal internalization¹⁷⁴. Omicron replicates quickly in the human bronchus¹⁷⁵, but it is less pathogenic, probably because the Omicron spike has an altered preference for cathepsin-mediated endosomal entry¹⁷⁶.

Camostat mesylate and nafamostat mesylate, approved in Japan for the treatment of noninfectious conditions such as pancreatitis, are oral serine protease inhibitors that target TMPRSS2 to block the membrane fusion of SARS-CoV-2 (Fig. 7b) in cell culture and animal models^168,177. However, two double-blind randomized placebo-controlled trials independently showed no clinical benefit of camostat mesylate among hospitalized adults with COVID-19 (NCT04657497, NCT04321096). Another two open-label randomized controlled trials also consistently reported no benefit of nafamostat mesylate among inpatients with COVID-19 (NCT04623021, NCT04473053). Other TMPRSS2 inhibitors (such as N-0385, avoralstat, MM3122), cathepsin L inhibitors (such as E-64d, K777 and Z-FY-CHO) and furin inhibitors (such as decanoyl-RVKR-CMK) may suppress spike cleavage to inhibit SARS-CoV-2 replication in cell culture and/or animal models (Supplementary Table 3). Nevertheless, applications of antiviral inhibitors targeting a single cellular protease remain a challenge because SARS-CoV-2 uses multiple entry pathways in a cell-type-dependent manner. In general, single-protein blockade of cellular proteases might be insufficient for complete virus inhibition, while a combination of multiple protease inhibitors usually causes severe toxicity.

Other host proteins

In addition to ACE2 and cellular proteases, many host proteins such as farnesoid X receptor¹⁷⁸, bromodomain-containing protein 2 (ref. ¹⁷⁹), caspase-6 (ref. ¹⁸⁰), CD147 (ref. ¹⁸¹), eukaryotic translation elongation factor 1A¹⁸², glycogen synthase kinase 3 (ref. ¹⁸³) and transmembrane protein 16F¹⁸⁴ have been explored for the development of anti-SARS-CoV-2 agents (Supplementary Table 3). Most such agents are in preclinical development, with a few having entered clinical trials. Sabizabulin, a microtubule disruptor with potential antiviral and anti-inflammatory activities, reduced all-cause mortality by day 15, 29 and 60 in a small cohort of high-risk adults hospitalized with moderate-to-severe COVID-19 (ref. ¹⁸⁵). Meplazumab, a humanized anti-CD147 IgG2 mAb, plus standard care reduced the 29-day mortality and viral loads in a phase II/III study of inpatients with severe COVID-19 (ref. ¹⁸⁶). In theory, inhibitors targeted at conserved host proteins overcome drug resistance, but their efficacy and safety profiles require evaluation. Future development of host-targeted inhibitors may focus on host proteins that are indispensable for the viral life cycle.

Targeting immune and inflammatory responses and coagulation

SARS-CoV-2 infection induces dysfunctional immune responses and aggressive inflammatory responses that are often associated with severe manifestations, including fatal systemic inflammation, cytokine storm, multiorgan damage and acute respiratory distress syndrome^24,187,188. Repurposing a wide range of marketed immunomodulators and anticoagulants, as well as some investigational drugs, has been extensively explored to mitigate dysfunctional responses in patients with COVID-19 (refs. ^189,190). However, many of these agents have not resulted in meaningful beneficial effects in clinical trials (Supplementary Table 4), and this section focuses on those with conclusive evidence. Limitations of drug repurposing in the context of COVID-19 are discussed later.

Systemic corticosteroids

Systemic corticosteroids are widely available and affordable anti-inflammatory and immunosuppressive drugs for the treatment of autoimmune and inflammatory diseases¹⁹¹. Corticosteroids can be classified into glucocorticoids (such as dexamethasone, hydrocortisone, prednisolone and methylprednisolone) and mineralocorticoids (such as fludrocortisone). The former exert anti-inflammatory action and immune regulation with clinical benefits for inpatients with severe COVID-19 (refs. ^192,193). The latter bind to cellular mineralocorticoid receptors to regulate the salt and water balance¹⁹² and probably have no beneficial effect on COVID-19 outcomes¹⁹⁴.

Dexamethasone and hydrocortisone are now recommended³⁶, mostly for inpatients with COVID-19 who are receiving oxygen support (Table 1). Dexamethasone is the first glucocorticoid identified with clinical benefit among inpatients with severe COVID-19. Soon after the COVID-19 outbreak, the RECOVERY study showed that dexamethasone significantly reduced 28-day mortality among inpatients with COVID-19 who required respiratory support¹⁹⁵. Dexamethasone alone or combined with tocilizumab and antivirals is beneficial for treating moderate-to-severe or critical COVID-19 (ref. ¹⁹⁶). Yet, such a benefit was not observed among inpatients who did not require respiratory support¹⁹⁵, and dexamethasone even increases the risk of severe drug-related adverse events among inpatients with severe COVID-19 (ref. ¹⁹⁷). Unlike systemically administered dexamethasone, inhaled glucocorticoids such as budesonide^198,199 and ciclesonide^200,201 exhibited inconsistent findings in randomized clinical trials.

Systemic corticosteroid therapies are known to cause severe adverse effects such as osteoporosis, adrenal suppression, cardiovascular disease and hyperglycaemia, especially when used at high doses for a prolonged period²⁰². In fact, corticosteroid therapy represents a double-edged sword to treat COVID-19 because its immunosuppressive properties may harmfully suppress antiviral immune responses in humans, especially during early disease progression²⁰³. Further studies need to address the optimal dose and treatment timing of systemic glucocorticoids in patients with COVID-19 because their benefits probably depend on the timing of drug initiation, dosage and COVID-19 severity.

Janus kinase inhibitors

Janus kinases (JAK1, JAK2, JAK3, tyrosine kinase 2) belong to a family of receptor-associated tyrosine kinases that modulate immune responses by activating JAK–STAT signalling pathways and transcriptional regulation in response to extracellular cytokines, interferons and growth factors²⁰⁴. JAK inhibitors such as baricitinib and tofacitinib have already been approved for treating immune–mediated inflammatory diseases such as rheumatoid arthritis, and so are readily available for drug repurposing to reduce inflammation and suppress COVID-19-associated immune dysregulation^205,206.

In May 2022, the FDA approved a new indication for baricitinib in hospitalized adults with COVID-19 who require oxygen support (Table 1). The oral regimen of baricitinib (tofacitinib is an alternative option if baricitinib is unavailable) plus systemic glucocorticoids such as dexamethasone is recommended by the NIH and Infectious Diseases Society of America (IDSA) guidelines to inpatients with severe or critical COVID-19 under certain conditions (Box 1). The efficacy and safety of baricitinib in inpatients with COVID-19 have been shown in randomized phase III trials such as RECOVERY²⁰⁷, COV-BARRIER²⁰⁸ and ACTT-2 (ref. ²⁰⁹). Both RECOVERY and COV-BARRIER reported a benefit of baricitinib in reducing 28-day all-cause mortality^207,208. Adding baricitinib to remdesivir was superior to remdesivir alone in reducing recovery time and 28-day all-cause mortality²⁰⁹. With established safety profiles, baricitinib offers potential benefits for inpatients with COVID-19, especially the elderly²⁰⁵. The efficacy and safety of tofacitinib were shown in the STOP-COVID trial of 289 hospitalized adults mostly receiving glucocorticoids²¹⁰. The incidence of death or respiratory failure through day 28 was lower in the tofacitinib group than in the placebo group, although this study was not powered to detect a difference in mortality²¹⁰. The short-term use of tofacitinib and baricitinib is unlikely to be associated with off-target effects such as thrombosis, secondary infections and immunosuppression^208,209,210.

Other JAK inhibitors such as fostamatinib, nezulcitinib, ruxolitinib and pacritinib have been evaluated in COVID-19 trials. A phase II trial of 59 hospitalized patients showed the clinical benefits of fostamatinib (NCT04579393), and a phase III trial (NCT04629703) is ongoing. Nezulcitinib (TD-0903) reduced 28-day all-cause mortality in a phase II trial of 235 inpatients with severe COVID-19 (NCT04402866). Compared with placebo plus standard care, ruxolitinib plus standard care showed no clinical benefit for inpatients with COVID-19 in the phase III RUXCOVID trial (NCT04362137). The phase III PRE-VENT study reported no significant benefit of pacritinib over placebo among inpatients with severe COVID-19 (NCT04404361). Overall, JAK inhibitors alone are insufficient for treating COVID-19 (ref. ²¹¹), and the optimal timing of JAK inhibitor treatment requires further investigation.

Cytokine antagonists

More than 20 interleukin or interleukin receptor antagonists have been approved, mostly for the treatment of autoimmune and inflammatory diseases (Supplementary Table 5). Blockade of pro-inflammatory cytokines such as IL-6 and their receptors is a possible therapeutic strategy to reduce aggressive inflammatory responses and to mitigate exacerbated cytokine release in patients with COVID-19 (refs. ^24,187,188). Among the long list of cytokines and chemokines, IL-6 has been recognized as a pleiotropic cytokine strongly associated with COVID-19 severity²¹². Repurposing IL-6 receptor antagonists such as tocilizumab thus reduces inflammatory responses and improves clinical outcomes in inpatients with COVID-19 (ref. ²¹³). Based on the RECOVERY trial (see Related links), which involved 4,116 COVID-19 inpatients with hypoxia and systemic inflammation at baseline, adding tocilizumab to standard care (glucocorticoids in 82% of cases) improved 28-day hospital discharge, lowered 28-day all-cause mortality and reduced the percentage of patients reaching the composite end point of invasive mechanical ventilation or death²¹³. Nevertheless, compared with standard care, tocilizumab plus standard care (concomitant glucocorticoids in only 19% of cases) did not reduce 28-day mortality in a phase III trial of inpatients with severe COVID-19 pneumonia²¹⁴. In June 2021, tocilizumab was granted an EUA by the FDA for the treatment of COVID-19 inpatients receiving systemic corticosteroids and requiring supplemental oxygen (Table 1).

Apart from tocilizumab, many cytokine antagonists have been evaluated in COVID-19 trials. Clinical benefits of the IL-6 receptor antagonist sarilumab versus placebo or standard care have been indicated in a randomized platform trial called REMAP-CAP²¹⁵, whereas added value of sarilumab was absent in Sarilumab-COVID-19 (NCT04315298) and Sarilumab COVID-19 Global Study (NCT04327388). In the REMAP-CAP study, the 180-day all-cause mortality was reduced among critically ill adults in intensive care units who received sarilumab or tocilizumab during their COVID-19 hospitalization²¹⁶. Clazakizumab, an experimental IL-6 antagonist, improved clinical outcomes among COVID-19 inpatients with hyperinflammation²¹⁷.

Anakinra, an IL-1 receptor antagonist, reduced 28-day all-cause mortality and hospital stay of inpatients with COVID-19 in SAVE-MORE (NCT04680949) but failed to show clinical benefits in REMAP-CAP (NCT02735707) and CORIMUNO-ANA-1 (NCT04341584). Differing outcomes have also been seen with three experimental mAbs that inhibit granulocyte–macrophage colony-stimulating factor: lenzilumab in LIVE-AIR²¹⁸, gimsilumab in BREATHE²¹⁹ and namilumab in CATALYST²²⁰. Clinical benefits of canakinumab (an IL-1β antagonist) and secukinumab (an IL-17 antagonist) among severely ill inpatients have not been shown in the randomized trials CAN-COVID²²¹ and BISHOP²²², respectively. CERC-002, a human anti-LIGHT mAb, reduced serum levels of the LIGHT cytokine in a small study of inpatients with COVID-19-associated pneumonia and mild-to-moderate acute respiratory distress syndrome (NCT04412057). Infliximab, a tumour necrosis factor antagonist, reduced the 28-day all-cause mortality and improved 14-day clinical status in the phase III ACTIV-1 IM study (NCT04593940).

Why do IL-6 antagonists offer clinical benefits but other interleukin antagonists seem less effective? This may be explained by the fact that IL-6 concentrations are highly elevated in patients with severe-to-critical COVID-19, but other interleukins are less so^212,223. However, the administration of IL-6 (receptor) antagonists should be closely monitored based on serum cytokine levels, the timing of cytokine blockade and the optimal dose³⁶.

Interferon therapies

Type I interferons, such as interferon-α (IFNα) and IFNβ, are known for their important roles in antiviral immune responses against viral infections^224,225. Pegylated IFNα-2a/2b and IFNβ-1a have been approved for treating hepatitis infection and relapsing forms of multiple sclerosis, respectively⁵. Early treatment with IFNβ-1b plus remdesivir may shorten viral shedding and hospitalization in high-risk patients²²⁶. Peg-IFNλ-1a reduced the incidence of hospitalization or emergency department visit in the phase III TOGETHER study of outpatients with COVID-19 (ref. ²²⁷), whereas IFNβ-1a showed no benefit in reducing overall mortality, initiation of ventilation or duration of hospital stay among inpatients with COVID-19 (ref. ²²⁸). For inpatients requiring high-flow oxygen at baseline, IFNβ-1a even increased the frequency of adverse effects such as respiratory failure²²⁹.

Other anti-inflammatory agents

Non-steroidal anti-inflammatory agents can be considered as adjunctive therapy to mitigate SARS-CoV-2-induced hyperinflammation, potentially reducing the risk of progression to severe COVID-19 (ref. ²³⁰). Topotecan, an FDA-approved anticancer compound, inhibits human topoisomerase 1 to suppress SARS-CoV-2-induced lethal inflammation in animal models²³¹, and it is being evaluated in a phase I study (NCT05083000). Vilobelimab, an anti-C5a mAb that blocks the C5a–C5aR1 signalling axis to mitigate inflammation and coagulation²³², reduced 28-day all-cause mortality among mechanically ventilated inpatients with COVID-19 in the phase III PANAMO study²³³. In April 2023, the FDA granted an emergency use of vilobelimab in hospitalized adults with COVID-19 when initiated within 48 hours of oxygen support.

Anticoagulants

Many patients with COVID-19, especially those with severe illness, have a high risk of venous thromboembolism associated with poor clinical outcomes and even death²³⁴. Although anticoagulants do not inhibit SARS-CoV-2 replication, therapeutic and prophylactic use of anticoagulants such as apixaban, enoxaparin and rivaroxaban has been evaluated to reduce thromboembolism in hospitalized patients with COVID-19 (ref. ²³⁵). In a large-scale randomized trial of 2,219 non-critically ill inpatients, low-molecular-weight heparin versus usual care improved the probability of survival to hospital discharge with reduced use of cardiovascular or respiratory organ support²³⁶. After inpatients with COVID-19 were discharged from hospital, rivaroxaban 10 mg daily for 35 days also improved the primary outcomes among those patients with an increased risk of venous thromboembolism²³⁷. However, thromboprophylaxis is ineffective among COVID-19 outpatients receiving apixaban²³⁸, enoxaparin²³⁹ or rivaroxaban²⁴⁰. Furthermore, the phase III INSPIRATION trial does not support the routine prophylactic use of enoxaparin 1 mg kg⁻¹ daily among unselected inpatients with COVID-19 admitted to the intensive care unit²⁴¹.

The net effect of heparin probably depends on patient status, disease severity and timing of treatment initiation, but there is a growing consensus regarding the clinical use of low-molecular-weight heparin to reduce the risk of thromboembolism and bleeding complications in certain (non-pregnant, non-intensive care unit) inpatients with COVID-19 (refs. ^242,243). Enoxaparin is a preferred low-molecular-weight heparin to reduce thromboembolism among inpatients with moderate-to-critical COVID-19 (ref. ²⁴⁴). Optimal doses and timing of anticoagulants require further investigation.

Outlook and challenges

Treatment strategies for COVID-19

To date, more than ten antiviral agents have been marketed for COVID-19 treatment (Table 1). The treatment window of antiviral agents is probably limited to the viral phase of SARS-CoV-2 infection (Fig. 8). For outpatients with mild-to-moderate COVID-19, early antiviral treatment needs to reduce the risk of progression to severe COVID-19. However, current marketed antiviral agents, except for oral nirmatrelvir–ritonavir and molnupiravir, are delivered by injection often in hospitals and infusion centres, limiting their practical administration in outpatient and resource-limited settings. In addition to antiviral agents, over-the-counter medications such as acetaminophen (paracetamol) are also effective for relieving COVID-19 symptoms such as fever, although they cannot eliminate coronaviruses²⁴⁵.

**Fig. 8: Therapeutic strategies for COVID-19 and future coronavirus outbreaks.**

During the early stages of COVID-19, treatment with anti-inflammatory drugs and immunomodulators might be harmful owing to the suppression of immune responses and increased viral loads. But for hospitalized patients with severe or critical COVID-19, a synergistic benefit might be achieved using antiviral agents plus supportive interventions such as immunomodulators, anticoagulants and/or anti-inflammatory drugs (Table 1). For instance, dexamethasone and remdesivir provide a synergistic benefit for hospitalized patients requiring oxygen support²⁴⁶. Nevertheless, drug−drug interactions should be cautiously evaluated because many antiviral and non-antiviral drugs are frequently administered, especially for severely ill adults with pre-existing diseases. Pre-existing use of some drugs such as mTOR inhibitors that increase human susceptibility to SARS-CoV-2 infection²⁴⁷ should be discontinued, at least during the period of viral infection.

Antiviral drug resistance, often induced by amino acid substitutions in the drug-binding pockets, poses a challenge to the development of potent antiviral drugs against SARS-CoV-2 variants⁵. Clinical use of many mAbs (Table 1) is no longer recommended because of drug resistance conferred by Omicron variants³⁶. Some mutations may confer resistance to nirmatrelvir (such as E166V⁹²) and remdesivir (such as V792I²⁴⁸). These mutations are currently at a low prevalence in global SARS-CoV-2 isolates, but special care should be taken for high-risk populations such as severely immunocompromised patients with high titres of SARS-CoV-2 for a prolonged period^248,249. Based on lessons learned from HIV and HCV therapies, it could be possible to develop dual-drug or triple-drug combinations (such as a polymerase inhibitor and a protease inhibitor plus a pharmacokinetic booster) that effectively inhibit multiple viral targets to maximize the chance of efficacy and to reduce the risk of drug resistance, although drug−drug interactions and accumulated adverse effects must be evaluated^99,250. The potential of such combinations to provide additional clinical benefits requires investigation.

Drug repurposing for COVID-19 treatment

Given the urgency of identifying therapies for COVID-19 and the typical lengthy timelines of traditional drug development, drug repurposing — involving the screening of approved drugs or clinical-stage candidates²⁵¹ originally developed for other human diseases — has been extensively pursued to identify agents that either inhibit SARS-CoV-2 or mitigate the consequences of viral infection. The hope is that prior knowledge of PK/PD and safety profiles, delivery route, and formulation of the repurposing candidates could accelerate and de-risk their development. Drug repurposing is conceptually appealing in response to an emergent outbreak, but its implementation faces challenges. Here, we highlight lessons learned from the repurposing efforts so far.

First, repurposing candidates must be rigorously assessed in preclinical and clinical studies (Fig. 9), particularly when the biological rationale for repurposing a given candidate (for example, hydroxychloroquine) is not clear. In some cases, the rationale may be relatively strong when the principal mechanisms of drug action are similar between the original and the new applications. For example, repurposing RNA polymerase nucleos(t)ide drugs such as remdesivir and molnupiravir to inhibit viral RNA synthesis would be expected to have a relatively high probability of success, but it remains a trial-and-error endeavour to identify nucleos(t)ide analogues that escape the SARS-CoV-2 proofreading mechanism²⁵². By contrast, repurposing DNA polymerase inhibitors such as tenofovir to inhibit the RNA synthesis of SARS-CoV-2 is doomed to failure because of their different mechanisms of action. Moreover, HIV protease inhibitors such as lopinavir should not be repurposed for SARS-CoV-2 treatment²⁵³ owing to the lack of similarity between the drug-binding pockets in HIV and SARS-CoV-2 proteases. Except for nucleos(t)ide inhibitors such as tenofovir, ribavirin and lamivudine, other virus-targeted inhibitors have not been approved by the FDA to treat more than one infectious disease^5,6. They are not good repurposing candidates because their chemical structures are often designed to target a particular drug-binding pocket with high selectivity, and thus they are unlikely to have a similar level of potency against an unrelated target. Importantly, cationic amphiphilic drugs (such as hydroxychloroquine, azithromycin and amiodarone) that induce phospholipidosis should not be repurposed, because cellular phospholipidosis is often misinterpreted as antiviral efficacy²⁵⁴.

**Fig. 9: Strategies to combat coronavirus outbreaks.**

Second, we suggest that future repurposing efforts focus on candidates that meet the following criteria: a well-defined molecular mechanism of action that has a plausible therapeutic rationale; a high specificity for the envisaged target; strong initial evidence of activity from robust preclinical studies in suitable disease models and/or clinical case studies; and lack of severe toxicity (or if toxicity occurs, it should be remediable). Ideally, repurposed inhibitors should have a low likelihood of drug resistance, or if resistance emerges, it should be addressable. Large libraries of approved or clinical-stage agents with diverse bioactivity might be useful for antiviral drug screening, but such open-access libraries are currently lacking²⁵⁵.

Third, bearing in mind that most repurposing candidates tested for COVID-19 failed to show clinical benefits, precautions should be taken to avoid off-label use of existing drugs until robust evidence is available. Candidates that failed to show significant clinical benefits in COVID-19 trials include, but are not limited to, various drugs developed against other viruses, such as lopinavir–ritonavir, tenofovir disoproxil fumarate, tenofovir alafenamide, emtricitabine, baloxavir marboxil, sofosbuvir, daclatasvir and velpatasvir; and a wide range of therapies developed for other human diseases, such as (hydroxy)chloroquine, acetylcysteine, allogeneic mesenchymal cells, aspirin, atorvastatin, almitrine, aviptadil acetate, azithromycin, camostat mesylate, astegolimab, brensocatib, canakinumab, gimsilumab, siltuximab, otilimab, ciclesonide, clopidogrel, colchicine, dapagliflozin, fluticasone furoate, fluvoxamine, efmarodocokin alfa, imatinib, ivermectin, metformin, nicotine, nitazoxanide, pirfenidone, losartan, ticagrelor, telmisartan, vitamin C, vitamin D3 and zinc gluconate (Supplementary Table 4).

Development of new anti-SARS-CoV-2 drugs

Based on our extensive search, many agents (n = 712) have been reported to have anti-SARS-CoV-2 activity in preclinical and/or clinical studies (Supplementary Tables 1–3). Most of these agents are small molecules (53%), followed by antibodies (33%), peptide inhibitors (4%) and others (such as macromolecular inhibitors, RNA-based therapies⁸ and cell-based therapies²⁵⁶). Most agents (>90%) have not progressed towards clinical trials, and lead optimization is still required in most cases.

We have highlighted drug-binding pockets in nine viral proteins (spike, nucleocapsid, papain-like protease, NSP5, NSP12 to NSP16). Structural analyses of papain-like protease, NSP16, NSP14 exoribonuclease and NSP12 NiRAN have revealed homologous proteins in humans, raising toxicity concerns for potential drugs that target them. In contrast, NSP5 main protease, NSP12 RdRp and NSP15 endoribonuclease possess drug-binding pockets with no homologous structures in human proteins, making them promising targets for developing small-molecule inhibitors with high specificity and low toxicity. So far, small-molecule inhibitors of NSP5 and NSP12 RdRp have been authorized. Structural proteins such as spike and nucleocapsid undergo dynamic structural rearrangements, thus posing a challenge to developing small-molecule inhibitors. Anti-spike mAbs have been successfully developed, but most have compromised efficacy owing to the emergence of SARS-CoV-2 variants such as Omicron.

In theory, there is potential to develop pan-coronavirus inhibitors that target drug-binding pockets with highly conserved sequences and structures across multiple coronaviruses. Preclinical studies have indicated the pan-coronavirus potential of NSP12 inhibitors such as remdesivir²⁵⁷, molnupiravir¹¹⁵ and 6-72-2a²⁵⁸ in cell culture and/or animal models. The M^pro inhibitors such as nirmatrelvir⁷⁸, ensitrelvir⁸⁶ and GC376 (ref. ²⁵⁹) may have broad-spectrum profiles, although some of them showed lower activities against alphacoronaviruses (HCoV-229E, HCoV-NL63) compared with betacoronaviruses (SARS-CoV, SARS-CoV-2, MERS-CoV). Based on lessons learned from antiviral drug discovery over past decades^5,260, nucleos(t)ide analogues that mimic natural nucleos(t)ides to inhibit viral synthesis have a great potential for potent pan-coronavirus inhibition. Future efforts to expand the arsenal of pan-coronavirus agents with suitable characteristics for clinical trials are merited.

In vitro assays and animal models for drug screening

Successful antiviral development requires appropriate cell lines (such as human airway epithelial cells), in vitro assays (such as multi-cycle virus neutralization assays) and animal challenge models (such as transgenic mice, hamsters and rhesus macaques)^28,261,262. SARS-CoV-2 primarily infects ciliated and type 2 pneumocyte cells in the human lung²⁶³; therefore, differentiated primary airway epithelial cells are a good model, but their limited proliferative lifespan in cell culture requires improvement²⁶⁴. The African green monkey kidney cell line, Vero E6, is a popular cell line that supports SARS-CoV-2 replication, but nonhuman cell lines are not adequate²⁰, especially for screening antiviral prodrugs such as nucleos(t)ide inhibitors that require metabolic activation in human cells²⁶⁵. There are notable examples such as chloroquine and ivermectin — two repurposed drugs that have been shown to provide no clinical benefits for patients with COVID-19 (Supplementary Table 4) — for which clinical testing was initially proposed based on their inhibition of SARS-CoV-2 in Vero E6 cells²⁶⁶. However, their limited anti-SARS-CoV-2 activity was subsequently shown in human Calu-3 lung cells²⁶⁷, emphasizing the importance of using appropriate cell lines for antiviral screening. Standardized laboratory protocols and assays, ideally established for each virus family, are important for avoiding false-positive results. In addition, biosafety labs should be established for virus detection and antiviral screening, as the lack of such labs can be a bottleneck in the early stage of a pandemic.

COVID-19 clinical trials

In the past 3 years, hundreds of agents have been tested in more than 10,000 registered clinical trials for COVID-19. However, most trials have lacked either randomization and/or sufficient power needed to provide high-quality evidence of efficacy and safety²⁶⁸, and many were duplicative. Some small-scale trials have reported conflicting results with drugs such as hydroxychloroquine, resulting in wasted resources and potential toxicity. Many trials have not been designed with suitable clinical end points endorsed by regulatory agencies (Box 1) or could not meet protocol-specified procedures owing to difficulties such as self-isolation, travel limitations and the emergence of new variants with heterogeneous patterns of disease progression and severity²⁶⁹.

In the context of a rapidly evolving landscape during the pandemic, the establishment of conventional clinical trials faces challenges such as a lack of flexibility to change interventions, difficulty in recruiting enough patients and limited resources. Notably, many of the most useful clinical results have been identified through platform trials that address some of the limitations of conventional trials²⁶⁸. These large-scale long-term randomized platform trials, such as RECOVERY, Solidarity and REMAP-CAP (see Related links), use one master protocol to simultaneously evaluate multiple interventions against a common control group, with the flexibility of adding new interventions and updating the control group²⁷⁰. The ongoing RECOVERY trial, established in March 2020, is one of the most successful platform trials, enrolling more than 50,000 patients with COVID-19 to produce landmark evidence on the effectiveness of dexamethasone, baricitinib, tocilizumab and casirivimab–imdevimab. It also proved the lack of efficacy of hydroxychloroquine, lopinavir–ritonavir, azithromycin, aspirin, convalescent plasma, colchicine and dimethyl fumarate in patients with COVID-19. The success of RECOVERY relies on central randomization; broad, simple inclusion criteria; the simple, unambiguous primary outcome of all-cause mortality; no extraneous data or biological sample collection, as well as national support and pre-existing clinical-trials networks²⁷¹.

Long COVID

Many patients have experienced long-term effects from SARS-CoV-2 infection, known as post-COVID-19 conditions or ‘long COVID’²⁷². According to the WHO update in December 2022, a clinical case definition of long COVID is based on symptoms such as chronic fatigue syndrome, respiratory symptoms and cognitive dysfunction^273,274 that are persistent for 3 months or longer after SARS-CoV-2 infection and last for 2 months or longer with no other explanation. Although it has been postulated that prolonged antiviral treatment and vaccines might reduce the likelihood of long COVID^275,276, conclusive evidence from ongoing clinical studies is still required. A platform trial called STIMULATE-ICP (see Related links) has been established to evaluate long COVID interventions such as famotidine and loratidine (antihistamines), rivaroxaban (an anticoagulant) and colchicine (an immunomodulator). Many interventions such as remdesivir (NCT04978259), nirmatrelvir–ritonavir (NCT05595369), metformin (NCT04510194) ibudilast/pentoxifylline (NCT05513560), unfractionated heparin (NCT05204550), leronlimab (NCT04678830), montelukast (NCT04695704), apixaban/atorvastatin (NCT04801940), infliximab/imatinib (NCT05220280) and vortioxetine (NCT05047952) are also being explored for long COVID treatment. Because the exact mechanism of long COVID remains under investigation and no drug has been approved for long COVID²⁷⁷, current clinical practice (Box 1) mostly adopts supportive approaches, such as pulmonary and cardiac rehabilitation and physical exercise programmes, and symptom-based interventions such as antidepressants, anticoagulants and immunosuppressants to alleviate long COVID symptoms²⁷⁸.

Conclusions

So far, drug discovery efforts for COVID-19 have led to the authorization of three classes of antiviral drugs — small-molecule inhibitors of NSP5 protease and NSP12 RdRp, and mAbs that target spike— as well as several therapies that target host proteins to improve clinical outcomes (Table 1 and Box 1).

Effective treatment strategies that can be inexpensively and conveniently applied are still needed to tackle COVID-19, including those that can address drug resistance conferred by emerging variants, for which combination therapies could be explored. The development of pan-coronavirus inhibitors and their combinations, ideally delivered orally or by inhalation, could be valuable in combating SARS-CoV-2 variants, and the availability of such therapies would be highly desirable in preparation for future outbreaks of pathogenic coronaviruses.

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