Elbasvir
FDA-approved product (tablet, oral).
- Registered studies
- 50+
- Lab records
- 0
- Pathogens at ≥40%
- 3 of 4
Chemical structure
Existing / approved use
Documented · FDA, WHO, ChEMBLApproved for
- Chronic hepatitis C virus infection
- Viral disease
Indications ChEMBL records as approved, from FDA and DailyMed labels. Label ↗
- WHO therapeutic group
- Antivirals for treatment of hcv infections
- Anti-infective classification
- Classified as another kind of anti-infective (for example an antifungal, antiviral or antiparasitic medicine).WHO ATC J05AP10
Repurposing investigation
This medicine is being investigated here for AI-predicted antimicrobial activity against MRSA, E. coli and M. tuberculosis. It was surfaced computationally for further investigation; it is not an established treatment for these infections.
AI-predicted activity
AI prediction · nothing measured- MRSA47.1% AI-predicted activityAt or above the ≥40% mark this site uses to surface candidates.
- E. coli44.9% AI-predicted activityAt or above the ≥40% mark this site uses to surface candidates.
- K. pneumoniae27.8% AI-predicted activityBelow the ≥40% mark this site uses to surface candidates.
- M. tuberculosis69.1% AI-predicted activityAt or above the ≥40% mark this site uses to surface candidates.
A model’s estimate of laboratory activity against each pathogen species. It is not clinical effectiveness.
Evidence
Clinical and experimental
Documented evidenceClinical
50+registered studies name this medicine, for any condition. The registry search keeps the first 50, so there may be more. See them below.
Experimental
No evidence found
No laboratory measurement against the four pathogens in the ChEMBL records loaded here.
Docking
Computational · nothing measuredDihydrofolate reductase ↗ (E. coli)
Not yet docked: queued in the docking rundetails
KPC-2 carbapenemase ↗ (K. pneumoniae)
Not yet docked: queued in the docking rundetails
Enoyl-ACP reductase (InhA) ↗ (M. tuberculosis)
Not yet docked: queued in the docking rundetails
Dihydrofolate reductase ↗ (MRSA)
Not yet docked: queued in the docking rundetails
AutoDock Vina, one experimentally solved protein per pathogen. This project’s screening target is -7.0 kcal/mol, its own mark rather than a universal cutoff. A docking score is a structural hypothesis, not proof of binding, and requires experimental validation.
Other medicines to investigate
AI prediction · nothing measuredOther repurposing candidates: approved medicines besides Elbasvir with AI-predicted activity ≥40% against the chosen pathogen, leaving out existing antimicrobials. They are computational candidates for further investigation, not alternatives and not recommendations.
Sorted by AI-predicted activity, high to low. The order is not a ranking of which medicine is better.
- DactinomycinExisting use: Kidney Wilms tumor, Neoplasm95.6% AI-predicted activityagainst MRSALab records exist50+ registered studies
- TaurursodiolExisting use: Bile acids and derivatives79.6% AI-predicted activityagainst MRSA43 registered studies
- LinaclotideExisting use: Constipation, Constipation disorder, Irritable bowel syndrome74.5% AI-predicted activityagainst MRSA50+ registered studies
- PlecanatideExisting use: Constipation74.4% AI-predicted activityagainst MRSA15 registered studies
- OxytocinExisting use: Hemorrhage, Uterine Inertia74.2% AI-predicted activityagainst MRSA50+ registered studies
- PosaconazoleExisting use: Aspergillosis, Candidiasis, Coccidioidomycosis and 2 more72.2% AI-predicted activityagainst MRSA50+ registered studies
- SotorasibExisting use: Neoplasm, Non-small cell lung carcinoma70.6% AI-predicted activityagainst MRSA50+ registered studies
- TemsirolimusExisting use: Cancer, Clear cell renal carcinoma, Mantle cell lymphoma and 2 more70.1% AI-predicted activityagainst MRSA50+ registered studies
- Quizartinib DihydrochlorideExisting use: Acute myeloid leukemia, Myeloid leukemia70.0% AI-predicted activityagainst MRSA4 registered studies
- Irinotecan HydrochlorideExisting use: Adenocarcinoma, Cancer, Carcinoma and 4 more70.0% AI-predicted activityagainst MRSA50+ registered studies
- Deoxycholic AcidExisting use: Other dermatologicals69.3% AI-predicted activityagainst MRSA50+ registered studies
- ChenodiolExisting use: Cerebrotendinous xanthomatosis, Inborn errors of metabolism69.2% AI-predicted activityagainst MRSA30 registered studies
Registered studies
A registration describes a study; it does not establish a positive result.
Administration of Zepatier (Grazoprevir Plus Elbasvir) in Chronic Hemodialysis (HD) Patients With Hepatitis C
NCT03365635 · start 2019-09-22
Registered record
- Registry ID
- NCT03365635
- Conditions
- Hepatitis C; Hemodialysis; Nosocomial Infection
- Interventions
- Elbasvir 50 MG / Grazoprevir 100 MG [Zepatier]
- Study type
- INTERVENTIONAL
- Phase
- Phase 4
- Registry status
- Completed
- Start
- 2019-09-22
- Completion
- 2020-09-01
- Enrolment
- 6
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionHepatitis C; Hemodialysis; Nosocomial InfectionInterventionElbasvir 50 MG / Grazoprevir 100 MG [Zepatier]PhasePhase 4Registry statusCompletedZepatier in Patients with Substance Use
NCT04048850 · start 2019-09-20
Registered record
- Registry ID
- NCT04048850
- Conditions
- Hepatitis C; Hiv; Coinfection, HIV; Substance Use Disorders
- Interventions
- Elbasvir/Grazoprevir 50 MG-100 MG Oral Tablet [ZEPATIER]
- Study type
- OBSERVATIONAL
- Phase
- Not recorded
- Registry status
- Completed
- Start
- 2019-09-20
- Completion
- 2022-09-09
- Enrolment
- 25
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionHepatitis C; Hiv; Coinfection, HIV; Substance Use DisordersInterventionElbasvir/Grazoprevir 50 MG-100 MG Oral Tablet [ZEPATIER]PhaseNot recordedRegistry statusCompletedBioequivalence Study of Crushed Elbasvir/Grazoprevir Compared to the Whole Tablet
NCT03817619 · start 2019-03-28
Registered record
- Registry ID
- NCT03817619
- Conditions
- Hepatitis C; Deglutition Disorders
- Interventions
- Zepatier whole tablet; Zepatier crushed tablet
- Study type
- INTERVENTIONAL
- Phase
- Phase 1
- Registry status
- Completed
- Start
- 2019-03-28
- Completion
- 2019-07-30
- Enrolment
- 11
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionHepatitis C; Deglutition DisordersInterventionZepatier whole tablet; Zepatier crushed tabletPhasePhase 1Registry statusCompletedGrazoprevir/Elbasvir for Genotype 1b Chronic Hepatitis C After Liver or Kidney Transplantation
NCT03723824 · start 2019-02-14
Registered record
- Registry ID
- NCT03723824
- Conditions
- Chronic Hepatitis c; Liver Transplant Infection; Kidney Transplant Infection
- Interventions
- grazoprevir 100 mg/ elbasvir 50 mg, Zepatier®
- Study type
- INTERVENTIONAL
- Phase
- Phase 4
- Registry status
- Terminated
- Start
- 2019-02-14
- Completion
- 2021-03-13
- Enrolment
- 14
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionChronic Hepatitis c; Liver Transplant Infection; Kidney Transplant InfectionInterventiongrazoprevir 100 mg/ elbasvir 50 mg, Zepatier®PhasePhase 4Registry statusTerminatedA Prospective Cohort Study to Improve HCV Care in Dialysis Patients
NCT03791814 · start 2019-01-01
Registered record
- Registry ID
- NCT03791814
- Conditions
- Hepatitis C
- Interventions
- Zepatier
- Study type
- INTERVENTIONAL
- Phase
- Phase 4
- Registry status
- Withdrawn
- Start
- 2019-01-01
- Completion
- 2019-06-30
- Enrolment
- 0
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionHepatitis CInterventionZepatierPhasePhase 4Registry statusWithdrawnElbasvir/Grazoprevir Fixed-Dose Combination for 8 Weeks in G1b Treatment-Naïve, HCV-Infected Patients
NCT03496233 · start 2018-09-19
Registered record
- Registry ID
- NCT03496233
- Conditions
- Chronic HCV Hepatitis
- Interventions
- Elbasvir 50 MG / Grazoprevir 100 MG Oral Tablet [Zepatier]
- Study type
- INTERVENTIONAL
- Phase
- Phase 3
- Registry status
- Completed
- Start
- 2018-09-19
- Completion
- 2020-06-20
- Enrolment
- 75
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionChronic HCV HepatitisInterventionElbasvir 50 MG / Grazoprevir 100 MG Oral Tablet [Zepatier]PhasePhase 3Registry statusCompletedPreemptive Zepatier Treatment in Donor HCV Positive to Recipient HCV Negative Cardiac Transplant
NCT03026023 · start 2018-08-01
Registered record
- Registry ID
- NCT03026023
- Conditions
- Cardiac Transplant Disorder; Hepatitis C
- Interventions
- Combindation treatment with Grazoprevir and Elbasvir fixed dose combination tablet, with or without ribavirin
- Study type
- INTERVENTIONAL
- Phase
- Phase 4
- Registry status
- Withdrawn
- Start
- 2018-08-01
- Completion
- 2021-06-30
- Enrolment
- 0
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionCardiac Transplant Disorder; Hepatitis CInterventionCombindation treatment with Grazoprevir and Elbasvir fixed dose combination tablet, with or without ribavirinPhasePhase 4Registry statusWithdrawnA Single-arm Evaluation of the Effect of HCV Treatment on Cardiovascular Disease Risk
NCT03585101 · start 2018-08
Registered record
- Registry ID
- NCT03585101
- Conditions
- Hepatitis C
- Interventions
- Elbasvir/grazoprevir
- Study type
- INTERVENTIONAL
- Phase
- Phase 4
- Registry status
- Withdrawn
- Start
- 2018-08
- Completion
- 2020-04
- Enrolment
- 0
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionHepatitis CInterventionElbasvir/grazoprevirPhasePhase 4Registry statusWithdrawnEight Weeks of Elbasvir/Grazoprevir in the Treatment of HCV Genotype 4
NCT03578640 · start 2018-07-01
Registered record
- Registry ID
- NCT03578640
- Conditions
- Hepatitis C, Chronic
- Interventions
- Elbasvir, Grazoprevir 50-100Mg Oral Tablet
- Study type
- INTERVENTIONAL
- Phase
- Phase 3
- Registry status
- Completed
- Start
- 2018-07-01
- Completion
- 2020-06-30
- Enrolment
- 30
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionHepatitis C, ChronicInterventionElbasvir, Grazoprevir 50-100Mg Oral TabletPhasePhase 3Registry statusCompletedEBR/GZR for HCV-1b Patients Receiving Hemodialysis
NCT03420300 · start 2018-06-05
Registered record
- Registry ID
- NCT03420300
- Conditions
- Hepatitis C
- Interventions
- EBR/GZR
- Study type
- INTERVENTIONAL
- Phase
- Phase 4
- Registry status
- Completed
- Start
- 2018-06-05
- Completion
- 2020-02-03
- Enrolment
- 40
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionHepatitis CInterventionEBR/GZRPhasePhase 4Registry statusCompletedHepatitis C (HCV) Cure and Kidney Health
NCT03407703 · start 2018-03-27
Registered record
- Registry ID
- NCT03407703
- Conditions
- Hepatitis C
- Interventions
- Elbasvir / Grazoprevir Oral Tablet [Zepatier]
- Study type
- OBSERVATIONAL
- Phase
- Not recorded
- Registry status
- Unknown
- Start
- 2018-03-27
- Completion
- 2019-12-31
- Enrolment
- 50
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionHepatitis CInterventionElbasvir / Grazoprevir Oral Tablet [Zepatier]PhaseNot recordedRegistry statusUnknownThe Dublin Zepatier Study
NCT02895958 · start 2018-03-15
Registered record
- Registry ID
- NCT02895958
- Conditions
- Hepatitis C
- Interventions
- Zepatier
- Study type
- INTERVENTIONAL
- Phase
- Phase 4
- Registry status
- Terminated
- Start
- 2018-03-15
- Completion
- 2019-12-06
- Enrolment
- 3
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionHepatitis CInterventionZepatierPhasePhase 4Registry statusTerminatedGrazoprevir and Elbasvir Without Ribavirin for 12 Weeks in Patients With HCV-related Cryoglobulinemic Nephropathy
NCT03433326 · start 2018-03-01
Registered record
- Registry ID
- NCT03433326
- Conditions
- Hepatitis C; Cryoglobulinaemic Glomerulonephritis
- Interventions
- Elbasvir/Grazoprevir
- Study type
- OBSERVATIONAL
- Phase
- Not recorded
- Registry status
- Unknown
- Start
- 2018-03-01
- Completion
- 2018-12-31
- Enrolment
- 45
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionHepatitis C; Cryoglobulinaemic GlomerulonephritisInterventionElbasvir/GrazoprevirPhaseNot recordedRegistry statusUnknownGrazoprevir/Elbasvir for Treatment of Hepatitis C Virus Genotype 4 Post Kidney Transplant
NCT03359746 · start 2017-12-15
Registered record
- Registry ID
- NCT03359746
- Conditions
- Hepatitis C
- Interventions
- Grazoprevir/Elbasvir
- Study type
- INTERVENTIONAL
- Phase
- Phase 4
- Registry status
- Unknown
- Start
- 2017-12-15
- Completion
- 2018-12-31
- Enrolment
- 40
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionHepatitis CInterventionGrazoprevir/ElbasvirPhasePhase 4Registry statusUnknownEfficacy and Tolerability of Grazoprevir and Elbasvir in Patients With Chronic Genotype 1 HCV and HIV Co-infection
NCT03098121 · start 2017-10-20
Registered record
- Registry ID
- NCT03098121
- Conditions
- Chronic Hepatitis C
- Interventions
- grazoprevir and elbasvir
- Study type
- INTERVENTIONAL
- Phase
- Phase 4
- Registry status
- Completed
- Start
- 2017-10-20
- Completion
- 2018-11-30
- Enrolment
- 40
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionChronic Hepatitis CInterventiongrazoprevir and elbasvirPhasePhase 4Registry statusCompleted