Ribavirin
FDA-approved product (for solution, inhalation), marketed as Copegus, Rebetol, Ribasphere and 2 more.
- Registered studies
- 50+
- Lab records
- 2
- Pathogens at ≥40%
- 0 of 4
Chemical structure
Existing / approved use
Documented · FDA, WHO, ChEMBLApproved for
- Chronic hepatitis C virus infection
- Cirrhosis of liver
- Fibrosis
- Viral disease
Indications ChEMBL records as approved, from FDA and DailyMed labels. Label ↗
- WHO therapeutic group
- Antivirals for treatment of hcv infections
- FDA pharmacologic class
- Nucleoside Analog Antiviral FDA label ↗
- Anti-infective classification
- Classified as another kind of anti-infective (for example an antifungal, antiviral or antiparasitic medicine).WHO ATC J05AP01; FDA class Nucleoside Analog Antiviral
Repurposing investigation
No supported pathogen reaches ≥40% AI-predicted activity for Ribavirin, so it is not among the repurposing candidates. Its predictions are shown below.
AI-predicted activity
AI prediction · nothing measured- MRSA19.1% AI-predicted activityBelow the ≥40% mark this site uses to surface candidates.
- E. coli5.2% AI-predicted activityBelow the ≥40% mark this site uses to surface candidates. This medicine was in the model's training data, so this is recall, not a new prediction.
- K. pneumoniae5.4% AI-predicted activityBelow the ≥40% mark this site uses to surface candidates. This medicine was in the model's training data, so this is recall, not a new prediction.
- M. tuberculosis22.1% AI-predicted activityBelow 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
- E. coli: measured active in 0 of 1 lab record
- K. pneumoniae: measured active in 0 of 1 lab record
Show the 2 laboratory records, with sources
Loading records…
“Active” means the measured value reached this project’s laboratory cutoff (10 µM or stronger). A laboratory result does not show an effect in patients.
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 Ribavirin 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.
- DichlorphenamideExisting use: Glaucoma73.9% AI-predicted activityagainst M. tuberculosisLab records exist2 registered studies
- Tamsulosin HydrochlorideExisting use: Benign prostatic hyperplasia, Prostate carcinoma73.2% AI-predicted activityagainst M. tuberculosis50+ registered studies
- Thiethylperazine MalateExisting use: Allergic disease71.8% AI-predicted activityagainst M. tuberculosisNo documented evidence found
- SaquinavirExisting use: HIV infection, HIV-1 infection, Viral disease71.5% AI-predicted activityagainst M. tuberculosis50+ registered studies
- AvacopanExisting use: Anti-neutrophil antibody associated vasculitis, Anti-neutrophil cytoplasmic antibody-associated vasculitis, Granulomatosis with Polyangiitis and 1 more71.3% AI-predicted activityagainst M. tuberculosis26 registered studies
- Lasmiditan SuccinateExisting use: Migraine disorder71.0% AI-predicted activityagainst M. tuberculosisNo documented evidence found
- SotorasibExisting use: Neoplasm, Non-small cell lung carcinoma71.0% AI-predicted activityagainst M. tuberculosis50+ registered studies
- Vinblastine SulfateExisting use: Classic Hodgkin lymphoma, Fungal infectious disease, Hodgkins lymphoma and 3 more70.8% AI-predicted activityagainst M. tuberculosis50+ registered studies
- Haloperidol DecanoateExisting use: Conduct disorder, Mental or behavioural disorder, Psychosis and 4 more70.1% AI-predicted activityagainst M. tuberculosis50+ registered studies
- HydrochlorothiazideExisting use: Angina pectoris, Cardiovascular disease, Chronic kidney disease and 9 more70.1% AI-predicted activityagainst M. tuberculosis50+ registered studies
- TolvaptanExisting use: Autosomal dominant polycystic kidney disease, Cardiovascular disease, Congestive heart failure and 4 more70.0% AI-predicted activityagainst M. tuberculosis50+ registered studies
- Larotrectinib SulfateExisting use: Abdominal Neoplasms, Cancer, Metastasis and 1 more69.2% AI-predicted activityagainst M. tuberculosis5 registered studies
Registered studies
A registration describes a study; it does not establish a positive result.
Treatment of CKD Patients With HCV
NCT07770984 · start 2026-09-15
Registered record
- Registry ID
- NCT07770984
- Conditions
- HCV Infection ( Genotype 4) in CKD Patients
- Interventions
- SOF+DCV; OBV/PTV/r) ± ribavirin (RBV)
- Study type
- INTERVENTIONAL
- Phase
- Phase 2 / Phase 3
- Registry status
- Not yet recruiting
- Start
- 2026-09-15
- Completion
- 2027-05-15
- Enrolment
- 50
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionHCV Infection ( Genotype 4) in CKD PatientsInterventionSOF+DCV; OBV/PTV/r) ± ribavirin (RBV)PhasePhase 2 / Phase 3Registry statusNot yet recruitingNew Antiviral Drugs for Treatment of COVID-19
NCT04392427 · start 2020-10
Registered record
- Registry ID
- NCT04392427
- Conditions
- COVID; Drug Effect
- Interventions
- Treatment group: will receive a combination of Nitazoxanide, Ribavirin and Ivermectin for a duration of seven days :
- Study type
- INTERVENTIONAL
- Phase
- Phase 3
- Registry status
- Unknown
- Start
- 2020-10
- Completion
- 2022-05
- Enrolment
- 100
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionCOVID; Drug EffectInterventionTreatment group: will receive a combination of Nitazoxanide, Ribavirin and Ivermectin for a duration of seven days :PhasePhase 3Registry statusUnknownCardiovascular Function and Ribavirin PK/PD in Lassa Fever in Lassa Fever
NCT04285034 · start 2019-11-26
Registered record
- Registry ID
- NCT04285034
- Conditions
- Lassa Fever
- Interventions
- Not recorded
- Study type
- OBSERVATIONAL
- Phase
- Not recorded
- Registry status
- Completed
- Start
- 2019-11-26
- Completion
- 2021-07-15
- Enrolment
- 158
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionLassa FeverInterventionNot recordedPhaseNot recordedRegistry statusCompletedEffect Of DAAs For Treatment Of HCV On Normal Kidney
NCT03296930 · start 2017-10-01
Registered record
- Registry ID
- NCT03296930
- Conditions
- Antiviral Drug Adverse Reaction
- Interventions
- Sofosbuvir 400 MG Oral Tablet,; Ombitasvir/paritaprevir/ritonavir
- Study type
- INTERVENTIONAL
- Phase
- Phase 4
- Registry status
- Unknown
- Start
- 2017-10-01
- Completion
- 2018-10-31
- Enrolment
- 100
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionAntiviral Drug Adverse ReactionInterventionSofosbuvir 400 MG Oral Tablet,; Ombitasvir/paritaprevir/ritonavirPhasePhase 4Registry statusUnknownPilot Study Evaluate Efficacy of Grazoprevir + Elbasvir for 12 or 16 Weeks in Liver Transplant Recipients.
NCT02890719 · start 2016-08-03
Registered record
- Registry ID
- NCT02890719
- Conditions
- Liver Transplantation; Hepatitis C
- Interventions
- Grazoprevir 100 mg/day; Elbasvir 50 mg/d; Grazoprevir 100 mg/day; Elbasvir 50 mg/day; Ribavirin 1200 mg/day
- Study type
- INTERVENTIONAL
- Phase
- Phase 3
- Registry status
- Withdrawn
- Start
- 2016-08-03
- Completion
- 2017-06-01
- Enrolment
- 0
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionLiver Transplantation; Hepatitis CInterventionGrazoprevir 100 mg/day; Elbasvir 50 mg/d; Grazoprevir 100 mg/day; Elbasvir 50 mg/day +1 morePhasePhase 3Registry statusWithdrawnManagement of Patients With Hepatitis C in a Public Health Care Setting: The Punjab Model
NCT03488485 · start 2016-06-18
Registered record
- Registry ID
- NCT03488485
- Conditions
- Chronic Hepatitis c
- Interventions
- Direct Acting Antivirals
- Study type
- INTERVENTIONAL
- Phase
- Not applicable
- Registry status
- Unknown
- Start
- 2016-06-18
- Completion
- 2020-12
- Enrolment
- 50,000
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionChronic Hepatitis cInterventionDirect Acting AntiviralsPhaseNot applicableRegistry statusUnknownAn Observational/Non-interventional, Study of NS3/4a Protease and NS5A Protein of Hepatitis C Virus in Brazilian Participants With Chronic HCV Infection
NCT02597270 · start 2016-03
Registered record
- Registry ID
- NCT02597270
- Conditions
- Hepatitis C Virus
- Interventions
- Not recorded
- Study type
- OBSERVATIONAL
- Phase
- Not recorded
- Registry status
- Completed
- Start
- 2016-03
- Completion
- 2016-11
- Enrolment
- 239
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionHepatitis C VirusInterventionNot recordedPhaseNot recordedRegistry statusCompletedDirectly Observed Therapy for HCV in Chennai, India
NCT02541409 · start 2015-09
Registered record
- Registry ID
- NCT02541409
- Conditions
- Hepatitis C, Chronic
- Interventions
- Sofosbuvir; Pegylated Interferon alfa-2a; Ribavirin
- Study type
- INTERVENTIONAL
- Phase
- Phase 2
- Registry status
- Completed
- Start
- 2015-09
- Completion
- 2016-12
- Enrolment
- 50
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionHepatitis C, ChronicInterventionSofosbuvir; Pegylated Interferon alfa-2a; RibavirinPhasePhase 2Registry statusCompletedA Study of the Efficacy and Safety of PPI-668 (NS5A Inhibitor) Plus Sofosbuvir, With or Without Ribavirin, in Patients With Chronic Hepatitis C Genotype-4
NCT02371408 · start 2015-01
Registered record
- Registry ID
- NCT02371408
- Conditions
- Chronic Hepatitis C
- Interventions
- ravidasvir hydrochloride; sofosbuvir; ribavirin
- Study type
- INTERVENTIONAL
- Phase
- Phase 2 / Phase 3
- Registry status
- Unknown
- Start
- 2015-01
- Completion
- 2016-04
- Enrolment
- 300
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionChronic Hepatitis CInterventionravidasvir hydrochloride; sofosbuvir; ribavirinPhasePhase 2 / Phase 3Registry statusUnknownSafety and Efficacy of Sofosbuvir + Ribavirin in Adolescents and Children With Genotype 2 or 3 Chronic HCV Infection
NCT02175758 · start 2014-07-07
Registered record
- Registry ID
- NCT02175758
- Conditions
- Hepatitis C Virus Infection
- Interventions
- SOF; RBV
- Study type
- INTERVENTIONAL
- Phase
- Phase 2
- Registry status
- Completed
- Start
- 2014-07-07
- Completion
- 2018-09-13
- Enrolment
- 106
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionHepatitis C Virus InfectionInterventionSOF; RBVPhasePhase 2Registry statusCompletedEfficacy and Safety of Sofosbuvir+Ribavirin in Genotype 2 HCV-infected U.S. Veterans With Cirrhosis
NCT02128542 · start 2014-06
Registered record
- Registry ID
- NCT02128542
- Conditions
- Hepatitis C Virus Infection
- Interventions
- Sofosbuvir; RBV
- Study type
- INTERVENTIONAL
- Phase
- Phase 4
- Registry status
- Completed
- Start
- 2014-06
- Completion
- 2015-06
- Enrolment
- 66
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionHepatitis C Virus InfectionInterventionSofosbuvir; RBVPhasePhase 4Registry statusCompletedA Pilot Study to Assess the Efficacy and Safety of Folic Acid and/or Vitamin B Complex on Hepatitis C Infected Patients Treated With Pegylated Interferon and Ribavirin.
NCT02150291 · start 2014-05
Registered record
- Registry ID
- NCT02150291
- Conditions
- Hepatitis C
- Interventions
- Folic acid; Neurobion; placebo
- Study type
- INTERVENTIONAL
- Phase
- Phase 4
- Registry status
- Unknown
- Start
- 2014-05
- Completion
- 2015-11
- Enrolment
- 120
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionHepatitis CInterventionFolic acid; Neurobion; placeboPhasePhase 4Registry statusUnknownA Study to Evaluate the Safety and Antiviral Effect of ABT-450/Ritonavir and ABT-530 Coadministered With and Without Ribavirin in Adults With Genotype 3 Hepatitis C (HCV) Infection
NCT02068222 · start 2014-04
Registered record
- Registry ID
- NCT02068222
- Conditions
- Chronic Hepatitis C; Hepatitis C Virus
- Interventions
- ABT-450/ritonavir (r); ABT-530; Ribavirin (RBV)
- Study type
- INTERVENTIONAL
- Phase
- Phase 2
- Registry status
- Completed
- Start
- 2014-04
- Completion
- 2015-03
- Enrolment
- 10
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionChronic Hepatitis C; Hepatitis C VirusInterventionABT-450/ritonavir (r); ABT-530; Ribavirin (RBV)PhasePhase 2Registry statusCompletedEfficacy and Safety of Sofosbuvir Plus Ribavirin in Adults With Chronic HCV Infection
NCT02021643 · start 2013-12-10
Registered record
- Registry ID
- NCT02021643
- Conditions
- Chronic HCV Infection
- Interventions
- Sofosbuvir; RBV; PEG
- Study type
- INTERVENTIONAL
- Phase
- Phase 3
- Registry status
- Completed
- Start
- 2013-12-10
- Completion
- 2016-11-03
- Enrolment
- 687
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionChronic HCV InfectionInterventionSofosbuvir; RBV; PEGPhasePhase 3Registry statusCompletedTherapy With Asunaprevir, Daclatasvir, Ribavirin and Pegylated Interferon Alpha-2a in HCV Genotype 4-infected Patients Who Have Failed to a Previous Therapy With Peg-Interferon/Ribavirin (ANRS HC32 QUATTRO)
NCT02107365 · start 2013-11
Registered record
- Registry ID
- NCT02107365
- Conditions
- Hepatitis C Virus Genotype 4 Infection
- Interventions
- Asunaprevir; Daclatasvir; Ribavirin; Pegylated Interferon alpha-2a
- Study type
- INTERVENTIONAL
- Phase
- Phase 2
- Registry status
- Completed
- Start
- 2013-11
- Completion
- 2015-04
- Enrolment
- 60
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionHepatitis C Virus Genotype 4 InfectionInterventionAsunaprevir; Daclatasvir; Ribavirin; Pegylated Interferon alpha-2aPhasePhase 2Registry statusCompleted