Remdesivir
drug drugOn 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
| Field | Value |
|---|---|
| ChEMBL ID | CHEMBL4065616 |
| Name | Remdesivir |
| Type | Small molecule |
| Max phase | 4 |
| FDA approved | yes |
| PubChem CID | 121304016 |
| ChEBI | CHEBI:145994 |
| ATC | J05AB16 |
| Molecular formula | C27H35N6O8P |
| Molecular weight | 602.6 |
| InChIKey | RWWYLEGWBNMMLJ-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).
| Gene | Target | Action | pAffinity | Cancer dependency | UniProt |
|---|---|---|---|---|---|
| CoV RNA-dependent RNA polymerase | Inhibition | ||||
| 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):
| Target | pChembl | Type | Value | Unit | Activity ID |
|---|---|---|---|---|---|
| P0DTD1 | 6.14 | EC50 | 730 | nM | CHEMBL_ACT_25615948 |
| P0DTD1 | 5.98 | EC50 | 1050 | nM | CHEMBL_ACT_25615945 |
| P0DTD1 | 5.95 | EC50 | 1130 | nM | CHEMBL_ACT_29311266 |
| P0DTD1 | 5.92 | IC50 | 1190 | nM | CHEMBL_ACT_23254362 |
| P0DTD1 | 5.87 | EC50 | 1360 | nM | CHEMBL_ACT_29173669 |
| P0DTD1 | 5.81 | IC50 | 1560 | nM | CHEMBL_ACT_23254318 |
| P0DTD1 | 5.81 | EC50 | 1540 | nM | CHEMBL_ACT_29173662 |
| P0DTD1 | 5.79 | IC50 | 1640 | nM | CHEMBL_ACT_25099148 |
| P0DTD1 | 5.71 | EC50 | 1940 | nM | CHEMBL_ACT_29311332 |
| P0DTD1 | 5.51 | IC50 | 3110 | nM | CHEMBL_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).
| Indication | Phase | MONDO | EFO |
|---|---|---|---|
| severe acute respiratory syndrome | 4 | MONDO:0005091 | EFO:0000694 |
| viral infectious disease | 4 | MONDO:0005108 | EFO: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) | Phase | MONDO | EFO |
|---|---|---|---|
| pneumonia | 3 | MONDO:0005249 | EFO:0003106 |
| influenza | 3 | MONDO:0005812 | EFO:0007328 |
| Ebola hemorrhagic fever | 2 | MONDO:0005737 | EFO:0007243 |
| acute respiratory distress syndrome | 2 | MONDO:0006502 | EFO:1000637 |
| viral pneumonia | 1 | MONDO:0006012 | EFO: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
| Phase | Trials |
|---|---|
| PHASE3 | 34 |
| PHASE2 | 17 |
| Not specified | 15 |
| PHASE2/PHASE3 | 7 |
| PHASE4 | 6 |
| PHASE1/PHASE2 | 2 |
| PHASE1 | 2 |
| EARLY_PHASE1 | 1 |
Top trials by phase / activity
| NCT | Phase | Status | Title |
|---|---|---|---|
| NCT06792214 | PHASE4 | RECRUITING | Antiviral Strategies in the Prevention of Long-term Cardiovascular Outcomes Following COVID-19: The paxloviD/Remdesivir Effectiveness For the prEvention of loNg coviD Clinical Trial |
| NCT04738045 | PHASE4 | UNKNOWN | Comparison of Remdesivir Versus Lopinavir/ Ritonavir and Remdesivir Combination in COVID-19 Patients |
| NCT04779047 | PHASE4 | UNKNOWN | Comparative Therapeutic Efficacy and Safety of Different Antiviral and Anti Inflammatory Drugs in COVID-19 Patients. |
| NCT04978259 | PHASE4 | UNKNOWN | SOLIDARITY Finland Long-COVID (Remdesivir Long-term Follow-up Study of COVID Patients) |
| NCT05502081 | PHASE4 | COMPLETED | Clinical Study to Compare Efficacy and Safety of Casirivimab and Imdevimab Combination, Remdesivir and Favipravir in Hospitalized COVID-19 Patients |
| NCT05911906 | PHASE4 | COMPLETED | An Open-label, Clinical Feasibility Study of the Efficacy of Remdesivir for Long-COVID. |
| NCT02735707 | PHASE3 | RECRUITING | Randomized, Embedded, Multifactorial Adaptive Platform Trial for Community- Acquired Pneumonia |
| NCT04483960 | PHASE3 | ACTIVE_NOT_RECRUITING | Australasian COVID-19 Trial (ASCOT) ADAptive Platform Trial |
| NCT07013474 | PHASE3 | RECRUITING | A Study to Learn About the Study Medicine Ibuzatrelvir in Adults With COVID-19 Who Are Severely Immunocompromised |
| NCT03719586 | PHASE2/PHASE3 | COMPLETED | Investigational Therapeutics for the Treatment of People With Ebola Virus Disease |
| NCT04252664 | PHASE3 | SUSPENDED | A Trial of Remdesivir in Adults With Mild and Moderate COVID-19 |
| NCT04257656 | PHASE3 | TERMINATED | A Trial of Remdesivir in Adults With Severe COVID-19 |
| NCT04280705 | PHASE3 | COMPLETED | Adaptive COVID-19 Treatment Trial (ACTT) |
| NCT04292730 | PHASE3 | COMPLETED | Study 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 |
| NCT04292899 | PHASE3 | COMPLETED | Study to Evaluate the Safety and Antiviral Activity of Remdesivir (GS-5734™) in Participants With Severe Coronavirus Disease (COVID-19) |
| NCT04315948 | PHASE3 | COMPLETED | Trial of Treatments for COVID-19 in Hospitalized Adults |
| NCT04321616 | PHASE2/PHASE3 | UNKNOWN | The Efficacy of Different Anti-viral Drugs in COVID 19 Infected Patients |
| NCT04345419 | PHASE2/PHASE3 | COMPLETED | Remdesivir Efficacy in Coronavirus Disease |
| NCT04349410 | PHASE2/PHASE3 | COMPLETED | The Fleming [FMTVDM] Directed CoVid-19 Treatment Protocol |
| NCT04351724 | PHASE2/PHASE3 | UNKNOWN | Austrian CoronaVirus Adaptive Clinical Trial (COVID-19) |
| NCT04401579 | PHASE3 | COMPLETED | Adaptive COVID-19 Treatment Trial 2 (ACTT-2) |
| NCT04409262 | PHASE3 | COMPLETED | A Study to Evaluate the Efficacy and Safety of Remdesivir Plus Tocilizumab Compared With Remdesivir Plus Placebo in Hospitalized Participants With Severe COVID-19 Pneumonia |
| NCT04431453 | PHASE2/PHASE3 | COMPLETED | Study of Remdesivir in Participants Below 18 Years Old With COVID-19 |
| NCT04492475 | PHASE3 | COMPLETED | Adaptive COVID-19 Treatment Trial 3 (ACTT-3) |
| NCT04501978 | PHASE3 | COMPLETED | ACTIV-3: Therapeutics for Inpatients With COVID-19 |
| NCT04546581 | PHASE3 | COMPLETED | Inpatient Treatment of COVID-19 With Anti-Coronavirus Immunoglobulin (ITAC) |
| NCT04575064 | PHASE2/PHASE3 | WITHDRAWN | An International Randomized Trial of Additional Treatments for COVID-19 in Hospitalized Patients Who Are All Receiving the Local Standard of Care - WHO-SOLIDARITY-GERMANY |
| NCT04593940 | PHASE3 | COMPLETED | Immune Modulators for Treating COVID-19 |
| NCT04640168 | PHASE3 | COMPLETED | Adaptive COVID-19 Treatment Trial 4 (ACTT-4) |
| NCT04647669 | PHASE3 | UNKNOWN | World Health Organization (WHO) COVID-19 Solidarity Trial for COVID-19 Treatments |
| NCT04678739 | PHASE3 | COMPLETED | Efficacy and Safety of Remdesivir and Tociluzumab for the Management of Severe COVID-19: A Randomized Controlled Trial |
| NCT04693026 | PHASE3 | UNKNOWN | Efficacy of Ramdicivir and Baricitinib for the Treatment of Severe COVID 19 Patients |
| NCT04694612 | PHASE3 | UNKNOWN | Efficacy of Favipiravir in Treatment of Mild & Moderate COVID-19 Infection in Nepal |
| NCT04745351 | PHASE3 | TERMINATED | Study to Evaluate the Efficacy and Safety of Remdesivir in Participants With Severely Reduced Kidney Function Who Are Hospitalized for Coronavirus Disease 2019 (COVID-19) |
| NCT04784559 | PHASE3 | TERMINATED | Trial to Determine the Efficacy/Safety of Plitidepsin vs Control in Patients With Moderate COVID-19 Infection |
| NCT04832880 | PHASE3 | UNKNOWN | Factorial Randomized Trial of Rendesivir and Baricitinib Plus Dexamethasone for COVID-19 (the AMMURAVID Trial) |
| NCT04843761 | PHASE3 | COMPLETED | ACTIV-3b: Therapeutics for Severely Ill Inpatients With COVID-19 |
| NCT04853901 | PHASE3 | COMPLETED | Remdesivir Efficacy In Management Of COVID-19 Patients |
| NCT04970719 | PHASE3 | WITHDRAWN | Baricitinib in Hospitalized Covid-19 Patients With Diabetes Mellitus |
| NCT05185284 | PHASE3 | COMPLETED | Randomized Multicenter Study on the Efficacy and Safety of Favipiravir for Parenteral Administration Compared to Standard of Care in Hospitalized Patients With COVID-19 |
| NCT05780268 | PHASE3 | COMPLETED | LY3819253 (LY-CoV555) for Inpatients With COVID-19 (An ACTIV-3/TICO Treatment Trial) |
| NCT05780281 | PHASE3 | COMPLETED | VIR-7831 for Inpatients With COVID-19 (An ACTIV-3/TICO Treatment Trial) |
| NCT05780424 | PHASE3 | COMPLETED | BRII-196/BRII-198 for Inpatients With COVID-19 (An ACTIV-3/TICO Treatment Trial) |
| NCT05780437 | PHASE3 | COMPLETED | AZD7442 for Inpatients With COVID-19 (An ACTIV-3/TICO Treatment Trial) |
| NCT05780463 | PHASE3 | COMPLETED | MP0420 for Inpatients With COVID-19 (An ACTIV-3/TICO Treatment Trial) |
| NCT05780541 | PHASE3 | TERMINATED | PF-07304814 for Inpatients With COVID-19 (An ACTIV-3/TICO Treatment Trial) |
| NCT06729593 | PHASE3 | COMPLETED | Remdesivir for Severely Ill Inpatients With COVID-19 (An ACTIV-3b/TESICO Treatment Trial) |
| NCT04488081 | PHASE2 | ACTIVE_NOT_RECRUITING | I-SPY COVID-19 TRIAL: An Adaptive Platform Trial for Critically Ill Patients |
| NCT04746183 | PHASE1/PHASE2 | RECRUITING | AGILE (Early Phase Platform Trial for COVID-19) |
| NCT05041907 | PHASE2 | RECRUITING | Finding Treatments for COVID-19: A Trial of Antiviral Pharmacodynamics in Early Symptomatic COVID-19 (PLATCOV) |
| NCT05587894 | PHASE2 | RECRUITING | OPtimisation of Antiviral Therapy in Immunocompromised COVID-19 Patients: a Randomized Factorial Controlled Strategy Trial |
| NCT06551844 | PHASE2 | RECRUITING | Adaptive Dengue Antiviral Platform Trial |
| NCT06817889 | PHASE2 | RECRUITING | Remdesivir for the Treatment of Upper Respiratory Tract Infection Due to RSV in Immunocompromised Individuals |
| NCT06873633 | PHASE2 | RECRUITING | Safety, Pharmacokinetics, and Antiviral Activity of Remdesivir (VEKLURY®) in Hospitalized Children With RSV |
| NCT07197164 | PHASE2 | RECRUITING | Safety and Effectiveness of a Remdesivir Treatment to Prevent Severe COVID-19 in Kidney Transplant Patients |
| NCT02818582 | PHASE2 | COMPLETED | GS-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 |
| NCT04321993 | PHASE2 | UNKNOWN | Treatment of Moderate to Severe Coronavirus Disease (COVID-19) in Hospitalized Patients |
| NCT04385719 | PHASE2 | COMPLETED | Drug-drug Interactions Between Remdesivir and Commonly Used Antiretroviral Therapy |
| NCT04391309 | PHASE2 | TERMINATED | COVID-19 and Anti-CD14 Treatment Trial |
| NCT04410354 | PHASE2 | TERMINATED | Study of Merimepodib in Combination With Remdesivir in Adult Patients With Advanced COVID-19 |
| NCT04539262 | PHASE1/PHASE2 | COMPLETED | Study in Participants With Early Stage Coronavirus Disease 2019 (COVID-19) to Evaluate the Safety, Efficacy, and Pharmacokinetics of Remdesivir Administered by Inhalation |
| NCT04583956 | PHASE2 | COMPLETED | ACTIV-5 / Big Effect Trial (BET-A) for the Treatment of COVID-19 |
| NCT04583969 | PHASE2 | COMPLETED | ACTIV-5 / Big Effect Trial (BET-B) for the Treatment of COVID-19 |
| NCT04596839 | PHASE2 | COMPLETED | Antiviral Activity and Safety of Remdesivir in Bangladeshi Patients With Severe Coronavirus Disease (COVID-19) |
| NCT04647695 | PHASE2 | UNKNOWN | IFN-beta 1b and Remdesivir for COVID19 |
| NCT04988035 | PHASE2 | COMPLETED | ACTIV-5 / Big Effect Trial (BET-C) for the Treatment of COVID-19 |
| NCT05925140 | PHASE1 | UNKNOWN | LUSZ Treatment Efficacy in Hospitalized COVID-19 Patients |
| NCT06860282 | PHASE1 | COMPLETED | A Study of CX2101A Enteric-Coated Tablets in Healthy Chinese Adult Subjects |
| NCT04560231 | EARLY_PHASE1 | UNKNOWN | Remdesivir in COVID-19 Lahore General Hospital |
| NCT03511118 | Not specified | RECRUITING | Pharmacokinetics and Safety of Commonly Used Drugs in Lactating Women and Breastfed Infants |
| NCT04302766 | Not specified | NO_LONGER_AVAILABLE | Expanded Access Remdesivir (RDV; GS-5734™) |
| NCT04323761 | Not specified | APPROVED_FOR_MARKETING | Expanded Access Treatment Protocol: Remdesivir (RDV; GS-5734) for the Treatment of SARS-CoV2 (CoV) Infection (COVID-19) |
| NCT04365725 | Not specified | COMPLETED | Multicenter, Retrospective Study of the Effects of Remdesivir in the Treatment of Severe Covid-19 Infections |
| NCT04492501 | Not specified | COMPLETED | Investigational Treatments for COVID-19 in Tertiary Care Hospital of Pakistan |
| NCT04582266 | Not specified | COMPLETED | PK and Safety of Remdesivir for Treatment of COVID-19 in Pregnant and Non-Pregnant Women in the US |
| NCT04669990 | Not specified | UNKNOWN | Remdesivir and Convalescent Plasma Therapy for Treatment of COVID-19 Infection in Nepal : A Registry Study |
| NCT04727775 | Not specified | COMPLETED | Antiviral Drugs on the Treatment of SARS-CoV-2 |
| NCT04728880 | Not specified | UNKNOWN | Remdesivir in Adults With Covid-19: Mansoura University Hospital Experience |
| NCT04847622 | Not specified | COMPLETED | Study to Evaluate the Clinical Outcomes in Adults With Covid-19 Who Have Been Treated With Remdesivir. |
| NCT04854837 | Not specified | COMPLETED | Safety of Remdesivir Treatment in COVID-19 Patients Requiring Hemodialysis |
| NCT04865237 | Not specified | COMPLETED | SARS-CoV-2 Human Challenge Characterisation Study |
| NCT04871633 | Not specified | COMPLETED | Effectiveness of Remedesvir in COVID-19 Patients Presenting at Mayo Hospital Lahore |
| NCT05024006 | Not specified | COMPLETED | Public Health Emergency: SOLIDARITY TRIAL Philippines |
| NCT05222113 | Not specified | COMPLETED | OBSERVATIONAL 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.
Related molecules
Related molecules
No competitor molecules sharing a primary target (ChEMBL phase ≥2 or PubChem drug-class).
Related Atlas pages
- Indicated for: severe acute respiratory syndrome, viral infectious disease
- In clinical trials for: pneumonia, influenza, Ebola hemorrhagic fever, acute respiratory distress syndrome