Remdesivir

drug
On this page

Also known as GS 5734Gs-5734VekluryRemdesivir (GS-5734)

Summary

Remdesivir (CHEMBL4065616) is an approved small-molecule antiviral drug (ATC J05AB16); indicated across 9 conditions including severe acute respiratory syndrome and viral infectious disease.

At a glance

  • Status: Approved (max clinical phase 4)
  • Modality: Small molecule
  • ATC class: J05AB16
  • Indications: 9 conditions
  • Clinical trials: 84
  • Chemistry: 602.6 Da · C27H35N6O8P

Identifiers

Drug identity and classification

FieldValue
ChEMBL IDCHEMBL4065616
NameRemdesivir
TypeSmall molecule
Max phase4
FDA approvedyes
PubChem CID121304016
ChEBICHEBI:145994
ATCJ05AB16
Molecular formulaC27H35N6O8P
Molecular weight602.6
InChIKeyRWWYLEGWBNMMLJ-YSOARWBDSA-N

SMILES: CCC(CC)COC(=O)[C@H](C)N[P@](=O)(OC[C@@H]1[C@H]([C@H]([C@](O1)(C#N)C2=CC=C3N2N=CN=C3N)O)O)OC4=CC=CC=C4

IUPAC name: 2-ethylbutyl (2S)-2-[[[(2R,3S,4R,5R)-5-(4-aminopyrrolo[2,1-f][1,2,4]triazin-7-yl)-5-cyano-3,4-dihydroxyoxolan-2-yl]methoxy-phenoxyphosphoryl]amino]propanoate

ChEBI definition: A carboxylic ester resulting from the formal condensation of the carboxy group of N-[(S)-{[(2R,3S,4R,5R)-5-(4-aminopyrrolo[2,1-f][1,2,4]triazin-7-yl)-5-cyano-3,4-dihydroxytetrahydrofuran-2-yl]methoxy}(phenoxy)phosphoryl]-L-alanine with the hydroxy group of 2-ethylbutan-1-ol. A broad-spectrum antiviral prodrug with potent in vitro antiviral activity against a diverse panel of RNA viruses such as Ebola virus, MERS-CoV and SARS-CoV. It is currently in Phase III clinical trials for the treatment of Covid-19 in adults.

Pharmacological roles (ChEBI): antiviral drug, prodrug, anticoronaviral agent.

Also known as: GS 5734, Gs-5734, GS-5734, Remdesivir, Veklury, REMDESIVIR, Remdesivir (GS-5734)

Patent coverage: 3,210 distinct patent families (6,642 SureChEMBL compound mentions), from 1 matched compound structure(s). Mentions count patents naming the compound (not distinct inventions), so promiscuous / reference molecules inflate the mention figure — families are the dedup metric.

Targets

Targets

Primary targets (GtoPdb curated mechanism): the Cancer dependency column is the DepMap CRISPR fitness signal (% of screened cell lines dependent on the target).

GeneTargetActionpAffinityCancer dependencyUniProt
CoV RNA-dependent RNA polymeraseInhibition
Inhibition

Broader ChEMBL bioactivity targets: 1 (assay-derived). Sample: Replicase polyprotein 1ab.

Bioactivity

ChEMBL activities: 10 potent at pChembl ≥ 5 of 10 total. Top 100 by potency (10 = 0.1 nM, 6 = 1 µM):

TargetpChemblTypeValueUnitActivity ID
P0DTD16.14EC50730nMCHEMBL_ACT_25615948
P0DTD15.98EC501050nMCHEMBL_ACT_25615945
P0DTD15.95EC501130nMCHEMBL_ACT_29311266
P0DTD15.92IC501190nMCHEMBL_ACT_23254362
P0DTD15.87EC501360nMCHEMBL_ACT_29173669
P0DTD15.81IC501560nMCHEMBL_ACT_23254318
P0DTD15.81EC501540nMCHEMBL_ACT_29173662
P0DTD15.79IC501640nMCHEMBL_ACT_25099148
P0DTD15.71EC501940nMCHEMBL_ACT_29311332
P0DTD15.51IC503110nMCHEMBL_ACT_23254368

Target pathways

No target-pathway data for this drug (no mapped target genes).

Indications & clinical

Indications

2 approved indications. FDA phase 4, plus an anticancer drug’s labelled cancer uses (which ChEMBL often logs at phase 3).

IndicationPhaseMONDOEFO
severe acute respiratory syndrome4MONDO:0005091EFO:0000694
viral infectious disease4MONDO:0005108EFO:0000763

5 diseases in clinical trials (phase 1–3, investigational — not approved indications). Highest ChEMBL trial phase per disease; a non-cancer approved use is occasionally logged at phase 3 here.

Disease (in trials)PhaseMONDOEFO
pneumonia3MONDO:0005249EFO:0003106
influenza3MONDO:0005812EFO:0007328
Ebola hemorrhagic fever2MONDO:0005737EFO:0007243
acute respiratory distress syndrome2MONDO:0006502EFO:1000637
viral pneumonia1MONDO:0006012EFO:0007541

2 further indication records had no mapped disease name (EFO/MeSH-only) or were duplicates, and are omitted.

Clinical trials

Total trials: 84.

Phase distribution

PhaseTrials
PHASE334
PHASE217
Not specified15
PHASE2/PHASE37
PHASE46
PHASE1/PHASE22
PHASE12
EARLY_PHASE11

Top trials by phase / activity

NCTPhaseStatusTitle
NCT06792214PHASE4RECRUITINGAntiviral Strategies in the Prevention of Long-term Cardiovascular Outcomes Following COVID-19: The paxloviD/Remdesivir Effectiveness For the prEvention of loNg coviD Clinical Trial
NCT04738045PHASE4UNKNOWNComparison of Remdesivir Versus Lopinavir/ Ritonavir and Remdesivir Combination in COVID-19 Patients
NCT04779047PHASE4UNKNOWNComparative Therapeutic Efficacy and Safety of Different Antiviral and Anti Inflammatory Drugs in COVID-19 Patients.
NCT04978259PHASE4UNKNOWNSOLIDARITY Finland Long-COVID (Remdesivir Long-term Follow-up Study of COVID Patients)
NCT05502081PHASE4COMPLETEDClinical Study to Compare Efficacy and Safety of Casirivimab and Imdevimab Combination, Remdesivir and Favipravir in Hospitalized COVID-19 Patients
NCT05911906PHASE4COMPLETEDAn Open-label, Clinical Feasibility Study of the Efficacy of Remdesivir for Long-COVID.
NCT02735707PHASE3RECRUITINGRandomized, Embedded, Multifactorial Adaptive Platform Trial for Community- Acquired Pneumonia
NCT04483960PHASE3ACTIVE_NOT_RECRUITINGAustralasian COVID-19 Trial (ASCOT) ADAptive Platform Trial
NCT07013474PHASE3RECRUITINGA Study to Learn About the Study Medicine Ibuzatrelvir in Adults With COVID-19 Who Are Severely Immunocompromised
NCT03719586PHASE2/PHASE3COMPLETEDInvestigational Therapeutics for the Treatment of People With Ebola Virus Disease
NCT04252664PHASE3SUSPENDEDA Trial of Remdesivir in Adults With Mild and Moderate COVID-19
NCT04257656PHASE3TERMINATEDA Trial of Remdesivir in Adults With Severe COVID-19
NCT04280705PHASE3COMPLETEDAdaptive COVID-19 Treatment Trial (ACTT)
NCT04292730PHASE3COMPLETEDStudy to Evaluate the Safety and Antiviral Activity of Remdesivir (GS-5734™) in Participants With Moderate Coronavirus Disease (COVID-19) Compared to Standard of Care Treatment
NCT04292899PHASE3COMPLETEDStudy to Evaluate the Safety and Antiviral Activity of Remdesivir (GS-5734™) in Participants With Severe Coronavirus Disease (COVID-19)
NCT04315948PHASE3COMPLETEDTrial of Treatments for COVID-19 in Hospitalized Adults
NCT04321616PHASE2/PHASE3UNKNOWNThe Efficacy of Different Anti-viral Drugs in COVID 19 Infected Patients
NCT04345419PHASE2/PHASE3COMPLETEDRemdesivir Efficacy in Coronavirus Disease
NCT04349410PHASE2/PHASE3COMPLETEDThe Fleming [FMTVDM] Directed CoVid-19 Treatment Protocol
NCT04351724PHASE2/PHASE3UNKNOWNAustrian CoronaVirus Adaptive Clinical Trial (COVID-19)
NCT04401579PHASE3COMPLETEDAdaptive COVID-19 Treatment Trial 2 (ACTT-2)
NCT04409262PHASE3COMPLETEDA Study to Evaluate the Efficacy and Safety of Remdesivir Plus Tocilizumab Compared With Remdesivir Plus Placebo in Hospitalized Participants With Severe COVID-19 Pneumonia
NCT04431453PHASE2/PHASE3COMPLETEDStudy of Remdesivir in Participants Below 18 Years Old With COVID-19
NCT04492475PHASE3COMPLETEDAdaptive COVID-19 Treatment Trial 3 (ACTT-3)
NCT04501978PHASE3COMPLETEDACTIV-3: Therapeutics for Inpatients With COVID-19
NCT04546581PHASE3COMPLETEDInpatient Treatment of COVID-19 With Anti-Coronavirus Immunoglobulin (ITAC)
NCT04575064PHASE2/PHASE3WITHDRAWNAn International Randomized Trial of Additional Treatments for COVID-19 in Hospitalized Patients Who Are All Receiving the Local Standard of Care - WHO-SOLIDARITY-GERMANY
NCT04593940PHASE3COMPLETEDImmune Modulators for Treating COVID-19
NCT04640168PHASE3COMPLETEDAdaptive COVID-19 Treatment Trial 4 (ACTT-4)
NCT04647669PHASE3UNKNOWNWorld Health Organization (WHO) COVID-19 Solidarity Trial for COVID-19 Treatments
NCT04678739PHASE3COMPLETEDEfficacy and Safety of Remdesivir and Tociluzumab for the Management of Severe COVID-19: A Randomized Controlled Trial
NCT04693026PHASE3UNKNOWNEfficacy of Ramdicivir and Baricitinib for the Treatment of Severe COVID 19 Patients
NCT04694612PHASE3UNKNOWNEfficacy of Favipiravir in Treatment of Mild & Moderate COVID-19 Infection in Nepal
NCT04745351PHASE3TERMINATEDStudy to Evaluate the Efficacy and Safety of Remdesivir in Participants With Severely Reduced Kidney Function Who Are Hospitalized for Coronavirus Disease 2019 (COVID-19)
NCT04784559PHASE3TERMINATEDTrial to Determine the Efficacy/Safety of Plitidepsin vs Control in Patients With Moderate COVID-19 Infection
NCT04832880PHASE3UNKNOWNFactorial Randomized Trial of Rendesivir and Baricitinib Plus Dexamethasone for COVID-19 (the AMMURAVID Trial)
NCT04843761PHASE3COMPLETEDACTIV-3b: Therapeutics for Severely Ill Inpatients With COVID-19
NCT04853901PHASE3COMPLETEDRemdesivir Efficacy In Management Of COVID-19 Patients
NCT04970719PHASE3WITHDRAWNBaricitinib in Hospitalized Covid-19 Patients With Diabetes Mellitus
NCT05185284PHASE3COMPLETEDRandomized Multicenter Study on the Efficacy and Safety of Favipiravir for Parenteral Administration Compared to Standard of Care in Hospitalized Patients With COVID-19
NCT05780268PHASE3COMPLETEDLY3819253 (LY-CoV555) for Inpatients With COVID-19 (An ACTIV-3/TICO Treatment Trial)
NCT05780281PHASE3COMPLETEDVIR-7831 for Inpatients With COVID-19 (An ACTIV-3/TICO Treatment Trial)
NCT05780424PHASE3COMPLETEDBRII-196/BRII-198 for Inpatients With COVID-19 (An ACTIV-3/TICO Treatment Trial)
NCT05780437PHASE3COMPLETEDAZD7442 for Inpatients With COVID-19 (An ACTIV-3/TICO Treatment Trial)
NCT05780463PHASE3COMPLETEDMP0420 for Inpatients With COVID-19 (An ACTIV-3/TICO Treatment Trial)
NCT05780541PHASE3TERMINATEDPF-07304814 for Inpatients With COVID-19 (An ACTIV-3/TICO Treatment Trial)
NCT06729593PHASE3COMPLETEDRemdesivir for Severely Ill Inpatients With COVID-19 (An ACTIV-3b/TESICO Treatment Trial)
NCT04488081PHASE2ACTIVE_NOT_RECRUITINGI-SPY COVID-19 TRIAL: An Adaptive Platform Trial for Critically Ill Patients
NCT04746183PHASE1/PHASE2RECRUITINGAGILE (Early Phase Platform Trial for COVID-19)
NCT05041907PHASE2RECRUITINGFinding Treatments for COVID-19: A Trial of Antiviral Pharmacodynamics in Early Symptomatic COVID-19 (PLATCOV)
NCT05587894PHASE2RECRUITINGOPtimisation of Antiviral Therapy in Immunocompromised COVID-19 Patients: a Randomized Factorial Controlled Strategy Trial
NCT06551844PHASE2RECRUITINGAdaptive Dengue Antiviral Platform Trial
NCT06817889PHASE2RECRUITINGRemdesivir for the Treatment of Upper Respiratory Tract Infection Due to RSV in Immunocompromised Individuals
NCT06873633PHASE2RECRUITINGSafety, Pharmacokinetics, and Antiviral Activity of Remdesivir (VEKLURY®) in Hospitalized Children With RSV
NCT07197164PHASE2RECRUITINGSafety and Effectiveness of a Remdesivir Treatment to Prevent Severe COVID-19 in Kidney Transplant Patients
NCT02818582PHASE2COMPLETEDGS-5734 to Assess the Antiviral Activity, Longer-Term Clearance of Ebola Virus, and Safety in Male Ebola Survivors With Evidence of Ebola Virus Persistence in Semen
NCT04321993PHASE2UNKNOWNTreatment of Moderate to Severe Coronavirus Disease (COVID-19) in Hospitalized Patients
NCT04385719PHASE2COMPLETEDDrug-drug Interactions Between Remdesivir and Commonly Used Antiretroviral Therapy
NCT04391309PHASE2TERMINATEDCOVID-19 and Anti-CD14 Treatment Trial
NCT04410354PHASE2TERMINATEDStudy of Merimepodib in Combination With Remdesivir in Adult Patients With Advanced COVID-19
NCT04539262PHASE1/PHASE2COMPLETEDStudy in Participants With Early Stage Coronavirus Disease 2019 (COVID-19) to Evaluate the Safety, Efficacy, and Pharmacokinetics of Remdesivir Administered by Inhalation
NCT04583956PHASE2COMPLETEDACTIV-5 / Big Effect Trial (BET-A) for the Treatment of COVID-19
NCT04583969PHASE2COMPLETEDACTIV-5 / Big Effect Trial (BET-B) for the Treatment of COVID-19
NCT04596839PHASE2COMPLETEDAntiviral Activity and Safety of Remdesivir in Bangladeshi Patients With Severe Coronavirus Disease (COVID-19)
NCT04647695PHASE2UNKNOWNIFN-beta 1b and Remdesivir for COVID19
NCT04988035PHASE2COMPLETEDACTIV-5 / Big Effect Trial (BET-C) for the Treatment of COVID-19
NCT05925140PHASE1UNKNOWNLUSZ Treatment Efficacy in Hospitalized COVID-19 Patients
NCT06860282PHASE1COMPLETEDA Study of CX2101A Enteric-Coated Tablets in Healthy Chinese Adult Subjects
NCT04560231EARLY_PHASE1UNKNOWNRemdesivir in COVID-19 Lahore General Hospital
NCT03511118Not specifiedRECRUITINGPharmacokinetics and Safety of Commonly Used Drugs in Lactating Women and Breastfed Infants
NCT04302766Not specifiedNO_LONGER_AVAILABLEExpanded Access Remdesivir (RDV; GS-5734™)
NCT04323761Not specifiedAPPROVED_FOR_MARKETINGExpanded Access Treatment Protocol: Remdesivir (RDV; GS-5734) for the Treatment of SARS-CoV2 (CoV) Infection (COVID-19)
NCT04365725Not specifiedCOMPLETEDMulticenter, Retrospective Study of the Effects of Remdesivir in the Treatment of Severe Covid-19 Infections
NCT04492501Not specifiedCOMPLETEDInvestigational Treatments for COVID-19 in Tertiary Care Hospital of Pakistan
NCT04582266Not specifiedCOMPLETEDPK and Safety of Remdesivir for Treatment of COVID-19 in Pregnant and Non-Pregnant Women in the US
NCT04669990Not specifiedUNKNOWNRemdesivir and Convalescent Plasma Therapy for Treatment of COVID-19 Infection in Nepal : A Registry Study
NCT04727775Not specifiedCOMPLETEDAntiviral Drugs on the Treatment of SARS-CoV-2
NCT04728880Not specifiedUNKNOWNRemdesivir in Adults With Covid-19: Mansoura University Hospital Experience
NCT04847622Not specifiedCOMPLETEDStudy to Evaluate the Clinical Outcomes in Adults With Covid-19 Who Have Been Treated With Remdesivir.
NCT04854837Not specifiedCOMPLETEDSafety of Remdesivir Treatment in COVID-19 Patients Requiring Hemodialysis
NCT04865237Not specifiedCOMPLETEDSARS-CoV-2 Human Challenge Characterisation Study
NCT04871633Not specifiedCOMPLETEDEffectiveness of Remedesvir in COVID-19 Patients Presenting at Mayo Hospital Lahore
NCT05024006Not specifiedCOMPLETEDPublic Health Emergency: SOLIDARITY TRIAL Philippines
NCT05222113Not specifiedCOMPLETEDOBSERVATIONAL STUDY OF COMPARISON EFFECTIVITY BETWEEN REMDESIVIR AND FAVIPIRAVIR IN SURABAYA, INDONESIA

Clinical evidence (CIViC)

No CIViC predictive evidence (expected for non-precision-medicine drugs).

Pharmacology

Pharmacogenomics

No CPIC/DPWG dosing guideline or drug-level clinical/variant annotations in PharmGKB for this molecule.

No competitor molecules sharing a primary target (ChEMBL phase ≥2 or PubChem drug-class).