Ribavirin
drug drugOn this page
Also known as CopegusCotronakNSC-163039RebetolRibasphereRibavarinRibavirin biopartnersRibavirin mylanRibavirin tevaRibavirin teva pharma b.v.RibavirinaRibavirineRibapakRibofluranosyl carboxamideSCH 18908SCH-18908TribavirinVirazidVirazole
Summary
Ribavirin (CHEMBL1643) is an approved small-molecule antiviral agent (ATC J05AP01) targeting IMPDH1 and IMPDH2; indicated across 24 conditions including chronic hepatitis c virus infection and cirrhosis of liver.
At a glance
- Status: Approved (max clinical phase 4)
- Modality: Small molecule
- ATC class: J05AP01
- Targets: 2 (IMPDH1, IMPDH2)
- Indications: 24 conditions
- Clinical trials: 624
- Chemistry: 244.2 Da · C8H12N4O5
Identifiers
Drug identity and classification
| Field | Value |
|---|---|
| ChEMBL ID | CHEMBL1643 |
| Name | Ribavirin |
| Type | Small molecule |
| Max phase | 4 |
| FDA approved | yes |
| PubChem CID | 37542 |
| ChEBI | CHEBI:63580 |
| ATC | J05AP01 |
| Molecular formula | C8H12N4O5 |
| Molecular weight | 244.2 |
| InChIKey | IWUCXVSUMQZMFG-AFCXAGJDSA-N |
SMILES: C1=NC(=NN1[C@H]2[C@@H]([C@@H]([C@H](O2)CO)O)O)C(=O)N
IUPAC name: 1-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]-1,2,4-triazole-3-carboxamide
ChEBI definition: A 1-ribosyltriazole that is the 1-ribofuranosyl derivative of 1,2,4-triazole-3-carboxamide. A synthetic guanosine analogue, it is an inhibitor of HCV polymerase and possesses a broad spectrum of activity against DNA and RNA viruses.
Pharmacological roles (ChEBI): antiviral agent, antiinfective agent, EC 2.7.7.49 (RNA-directed DNA polymerase) inhibitor, anticoronaviral agent.
Other ChEBI roles (chemical / environmental): antimetabolite.
Also known as: Copegus, Cotronak, NSC-163039, Rebetol, Ribasphere, Ribavarin, Ribavirin, Ribavirin biopartners, Ribavirin mylan, Ribavirin teva, Ribavirin teva pharma b.v., Ribavirina
Patent coverage: 23,504 distinct patent families (78,049 SureChEMBL compound mentions), from 2 matched compound structure(s). One matched structure accounts for 78,047 (100%) of the total. 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 |
|---|---|---|---|---|---|
| IMPDH1 | inosine monophosphate dehydrogenase 1 | Inhibition | 6 | 8.8% | P20839 |
| IMPDH2 | inosine monophosphate dehydrogenase 2 | Inhibition | 6 | 48.5% | P12268 |
Broader ChEMBL bioactivity targets: 15 (assay-derived). Sample: Survival motor neuron protein, Prelamin-A/C, Thrombopoietin, Peripheral myelin protein 22, DNA topoisomerase 1, Thyrotropin receptor, Adenosine receptor A1, Alpha-galactosidase A, Muscarinic acetylcholine receptor M1, PA/PB1, Cytochrome P450 3A4, Aldehyde dehydrogenase 1A1, Adenosine receptor A1, RNA-directed RNA polymerase, Eukaryotic translation initiation factor 4E.
Bioactivity
ChEMBL activities: 7 potent at pChembl ≥ 5 of 21 total. Top 100 by potency (10 = 0.1 nM, 6 = 1 µM):
| Target | pChembl | Type | Value | Unit | Activity ID |
|---|---|---|---|---|---|
| LMNA | 8.4 | Potency | 4 | nM | CHEMBL_ACT_3647475 |
| P08482 | 7.3 | Potency | 50.1 | nM | CHEMBL_ACT_4807344 |
| CYP3A4 | 6.1 | Potency | 794.3 | nM | CHEMBL_ACT_4961408 |
| CYP3A4 | 6.1 | Potency | 794.3 | nM | CHEMBL_ACT_5030657 |
| Q60612 | 5.35 | Ki | 4430 | nM | CHEMBL_ACT_19108123 |
| ADORA1 | 5.13 | Ki | 7410 | nM | CHEMBL_ACT_19108096 |
| EIF4E | 5.08 | Kd | 8400 | nM | CHEMBL_ACT_25596511 |
Target pathways
Aggregated over 2 target gene(s): IMPDH1, IMPDH2.
Top Reactome pathways
14 total, by targets touching each:
| Pathway | Targets | Genes |
|---|---|---|
| Metabolism | 2 | IMPDH1, IMPDH2 |
| Metabolism of nucleotides | 2 | IMPDH1, IMPDH2 |
| Disease | 2 | IMPDH1, IMPDH2 |
| Innate Immune System | 2 | IMPDH1, IMPDH2 |
| Immune System | 2 | IMPDH1, IMPDH2 |
| Infectious disease | 2 | IMPDH1, IMPDH2 |
| Neutrophil degranulation | 2 | IMPDH1, IMPDH2 |
| Purine ribonucleoside monophosphate biosynthesis | 2 | IMPDH1, IMPDH2 |
| Nucleotide biosynthesis | 2 | IMPDH1, IMPDH2 |
| Potential therapeutics for SARS | 2 | IMPDH1, IMPDH2 |
| SARS-CoV Infections | 2 | IMPDH1, IMPDH2 |
| Drug ADME | 2 | IMPDH1, IMPDH2 |
| Azathioprine ADME | 2 | IMPDH1, IMPDH2 |
| Viral Infection Pathways | 2 | IMPDH1, IMPDH2 |
Dominant GO biological processes
| GO term | Targets |
|---|---|
| GMP biosynthetic process | 2 |
| GTP biosynthetic process | 2 |
| lymphocyte proliferation | 2 |
| ‘de novo’ XMP biosynthetic process | 2 |
| purine nucleotide biosynthetic process | 2 |
| circadian rhythm | 1 |
| cellular response to interleukin-4 | 1 |
Indications & clinical
Indications
3 approved indications. FDA phase 4, plus an anticancer drug’s labelled cancer uses (which ChEMBL often logs at phase 3).
| Indication | Phase | MONDO | EFO |
|---|---|---|---|
| chronic hepatitis C virus infection | 4 | MONDO:0005354 | EFO:0004220 |
| cirrhosis of liver | 4 | MONDO:0005155 | EFO:0001422 |
| viral infectious disease | 4 | MONDO:0005108 | EFO:0000763 |
17 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 |
|---|---|---|---|
| hepatitis C virus infection | 3 | MONDO:0005231 | EFO:0003047 |
| hepatitis B virus infection | 3 | MONDO:0005344 | EFO:0004197 |
| HIV infectious disease | 3 | MONDO:0005109 | EFO:0000764 |
| chronic hepatitis B virus infection | 3 | MONDO:0005366 | EFO:0004239 |
| respiratory syncytial virus infectious disease | 3 | MONDO:0001577 | EFO:1001413 |
| hepatitis | 3 | MONDO:0002251 | HP:0012115 |
| severe acute respiratory syndrome | 3 | MONDO:0005091 | EFO:0000694 |
| depressive disorder | 3 | MONDO:0002050 | MONDO:0002050 |
| acute myeloid leukemia | 2 | MONDO:0018874 | EFO:0000222 |
| hepatitis D virus infection | 2 | MONDO:0005789 | EFO:0007304 |
| Japanese encephalitis | 2 | MONDO:0019209 | EFO:0007332 |
| thrombocytopenia | 2 | MONDO:0002049 | HP:0001873 |
| influenza | 2 | MONDO:0005812 | EFO:0007328 |
| Lassa fever | 2 | MONDO:0005820 | EFO:0007338 |
| type 1 diabetes mellitus | 2 | MONDO:0005147 | MONDO:0005147 |
| neoplasm | 1 | MONDO:0005070 | EFO:0000616 |
| breast neoplasm | 1 | MONDO:0021100 | MONDO:0007254 |
4 further indication records had no mapped disease name (EFO/MeSH-only) or were duplicates, and are omitted.
Clinical trials
Total trials: 624.
Phase distribution
| Phase | Trials |
|---|---|
| PHASE2 | 204 |
| PHASE3 | 167 |
| PHASE4 | 112 |
| Not specified | 80 |
| PHASE1 | 24 |
| PHASE2/PHASE3 | 21 |
| PHASE1/PHASE2 | 14 |
| EARLY_PHASE1 | 2 |
Top trials by phase / activity
| NCT | Phase | Status | Title |
|---|---|---|---|
| NCT02460133 | PHASE4 | ACTIVE_NOT_RECRUITING | Understanding HCV Reinfection Rates in an Incarcerated Population After Cure With Interferon Free HCV Treatment |
| NCT00001854 | PHASE4 | COMPLETED | Long-Term Therapy With Ribavirin for Chronic Hepatitis C |
| NCT00056862 | PHASE4 | COMPLETED | Low-Dose Peginterferon and Ribavirin to Treat Chronic Hepatitis C in Patients Infected With HCV Genotype 2 or 3 |
| NCT00077636 | PHASE4 | COMPLETED | ACCELERATE Study - A Study of PEGASYS (Peginterferon Alfa-2a (40KD)) in Combination With COPEGUS (Ribavirin) in Interferon-Naive Patients With Chronic Hepatitis C (CHC) Infection. |
| NCT00077649 | PHASE4 | COMPLETED | A Study of PEGASYS (Peginterferon Alfa-2a (40KD)) in Combination With COPEGUS (Ribavirin) in Interferon-Naive Patients With Chronic Hepatitis C Infection (CHC). |
| NCT00087568 | PHASE4 | COMPLETED | A Study of PEGASYS (Peginterferon Alfa-2a (40KD)) in Combination With Ribavirin in Patients With Chronic Hepatitis C (CHC) Previously Treated With PEG-Intron + Ribavirin |
| NCT00087594 | PHASE4 | COMPLETED | A Study of PEGASYS (Peginterferon Alfa-2a (40KD)) in Combination With Copegus (Ribavirin) in Patients With Chronic Hepatitis C (CHC) Enrolled in a Methadone Maintenance Treatment Program. |
| NCT00087607 | PHASE4 | COMPLETED | Peak Study - A Study of Pegasys (Peginterferon Alfa-2a (40KD)) in Combination With Copegus (Ribavirin) in Interferon-Naive Patients With Chronic Hepatitis C (CHC). |
| NCT00087633 | PHASE4 | COMPLETED | PHOENIX Study - A Study of PEGASYS (Peginterferon Alfa-2a (40KD)) and COPEGUS (Ribavirin) Administered After Liver Transplantation for Hepatitis C. |
| NCT00087646 | PHASE4 | COMPLETED | REPEAT Study - A Study of PEGASYS (Peginterferon Alfa-2a (40KD)) Therapy in Combination With COPEGUS (Ribavirin) in Patients With Chronic Hepatitis C (CHC) Who Did Not Respond to Previous PegIntron (Peginterferon Alfa-2b (12KD))/Ribavirin Combination Therapy |
| NCT00107653 | PHASE4 | COMPLETED | Latino Study - A Study of PEGASYS (Peginterferon Alfa-2a (40KD)) and COPEGUS (Ribavirin) in Treatment-Naive Patients With Chronic Hepatitis C-Genotype 1. |
| NCT00143000 | PHASE4 | COMPLETED | Multicenter Study Evaluating 12 Versus 24 Weeks Therapy With Peginterferon and Ribavirin for Hepatitis C Virus (HCV) Genotype 2 or 3 |
| NCT00148031 | PHASE4 | COMPLETED | Improving Hepatitis C Treatment in Injection Drug Users |
| NCT00167557 | PHASE4 | WITHDRAWN | Orthotopic Liver Transplant (OLT) Recipients With Hepatitis C Virus (HCV) Under Preemptive Treatment |
| NCT00192647 | PHASE4 | COMPLETED | A Study of Induction Dosing With Peginterferon Alfa-2a and Ribavirin in Participants With Chronic Hepatitis C (CHC) Genotype 1 Infection |
| NCT00202839 | PHASE4 | COMPLETED | Peg-Intron/Ribavirin in G 1 HCV for Non-Extended Versus 24 Week Extended Treatment After 24 Weeks (Study P04144)(COMPLETED) |
| NCT00203606 | PHASE4 | COMPLETED | Pegylated Interferon Plus Ribavirin in the Treatment of Active and Past Intravenous Drug Users Infected With Hepatitis C |
| NCT00207311 | PHASE4 | COMPLETED | Study for the Treatment of Significant Steatosis With Xenical Followed by Treatment of Hepatitis C With Pegasys/Copegus |
| NCT00207363 | PHASE4 | COMPLETED | Does Induction PEG-Intron in Combination With Rebetol Enhance the Sustained Response Rates in Patients With CHC |
| NCT00241618 | PHASE4 | COMPLETED | Timing and Duration of Acute Hepatitis C Treatment |
| NCT00255008 | PHASE4 | TERMINATED | Peg-Intron and Rebetol Therapy in Treatment of Naive Hepatitis C Patients: A Comparison of Race and Genotype on Treatment Outcome (Study P04212) |
| NCT00255034 | PHASE4 | TERMINATED | Effects of 48 Weeks Versus 24 Weeks of Therapy With Peg-Intron/Ribavirin in Patients With Chronic Hepatitis C, Genotype 3 (Study P04143)(TERMINATED) |
| NCT00274495 | PHASE4 | TERMINATED | Assessing the Efficacy and Safety of Rosiglitazone Added to Standard Therapy for Hepatitis C Genotype 1 With Fatty Liver |
| NCT00275548 | PHASE4 | COMPLETED | Safety and Effectiveness Using Pegasys and Copegus in Recipients of Liver Transplantation With Hepatitis C |
| NCT00277862 | PHASE4 | COMPLETED | Pegylated Interferon and Ribavirin Therapy in Chronic Hepatitis Genotype 4 |
| NCT00351403 | PHASE4 | COMPLETED | Individually Adapted Therapy Duration for the Treatment of Chronic Hepatitis C Genotype 1 Infection |
| NCT00353418 | PHASE4 | COMPLETED | A Study of PEGASYS (Peginterferon Alfa-2a (40KD)) Plus COPEGUS (Ribavirin) in Patients With Chronic Hepatitis C (CHC) Genotype 1 and Human Immunodeficiency Virus-1 (HIV-1) Co-infection |
| NCT00356486 | PHASE4 | COMPLETED | Viral Kinetics of Treatment With Peginterferon Alpha-2a, Ribavirin and Epoetin β in Patients Coinfected HCV/HIV |
| NCT00375661 | PHASE4 | COMPLETED | Low-dose Peg-interferon Plus Ribavirin (IFN/RBV) for Prevention of Hepatocellular Carcinoma (HCC) Recurrence in Patients Who Had Surgery to Remove Primary HCC |
| NCT00383864 | PHASE4 | COMPLETED | Pegylated Interferon and Ribavirin in Hepatitis C Virus Infection After Liver Transplantation. |
| NCT00394277 | PHASE4 | COMPLETED | A Study of Induction Dosing With PEGASYS (Peginterferon Alfa-2a [40KD]) Plus Copegus in Treatment-Naive Patients With Chronic Hepatitis C |
| NCT00412334 | PHASE4 | COMPLETED | SYREN Study: A Study of PEGASYS (Peginterferon Alfa-2a (40KD)) Plus Copegus (Ribavirin) in Non-Responder Patients With Chronic Hepatitis C (CHC) Genotype 1. |
| NCT00456248 | PHASE4 | TERMINATED | Infergen and Ribavirin Treatment of Patients With HCV Who Achieved Partial Response to Peginterferon-alfa and Ribavirin |
| NCT00475072 | PHASE4 | COMPLETED | A Study of PEGASYS (Peginterferon Alfa-2a (40KD)) Plus Ribavirin in Hemophiliac Patients With Chronic Hepatitis C. |
| NCT00484328 | PHASE4 | COMPLETED | Ribavirin, Its Dosing Regime |
| NCT00491179 | PHASE4 | COMPLETED | Retreatment of Dialysis Patients With Chronic Hepatitis C With Pegylated Interferon Alfa-2a Plus Low Dose Ribavirin |
| NCT00491244 | PHASE4 | COMPLETED | Pegylated Interferon Alfa-2a Plus Low Dose Ribavirin for Treatment-Naïve Hemodialysis Patients With Chronic Hepatitis C |
| NCT00493805 | PHASE4 | TERMINATED | Study of Response in Chronic Hepatitis C (CHC) Participants Genotype 1 With Insulin Resistance and Prolonged Treatment Duration in Late Responders (P04823/MK-4031-303) |
| NCT00500578 | PHASE4 | COMPLETED | Intermittent Use of Aerosolized Ribavirin for Treatment of RSV |
| NCT00502099 | PHASE4 | COMPLETED | Comparison of Pegasys Versus Peg-Intron for Treatment of Chronic Hepatitis C Genotype 4 |
| NCT00526448 | PHASE4 | UNKNOWN | Phase IV Study to Evaluate the Efficacy/Safety to Extend Treatment and High Dose of Ribavirin in co-Infected Patients |
| NCT00540345 | PHASE4 | COMPLETED | Four Arms, Multicenter Study of Tailored Regimens With Peginterferon Plus Ribavirin for Genotype 2 Chronic Hepatitis C |
| NCT00545233 | PHASE4 | COMPLETED | A Study of PEGASYS (Peginterferon Alfa-2a (40KD)) Plus COPEGUS (Ribavirin) With or Without Pioglitazone in Treatment-Naive Patients With Chronic Hepatitis C and Insulin Resistance. |
| NCT00553930 | PHASE4 | COMPLETED | Low Dose Peginterferon-α 2a for Chronic Hepatitis C, Genotypes 2 or 3, in HIV-coinfected Patients |
| NCT00560274 | PHASE4 | COMPLETED | A Study of NeoRecormon (Epoetin Beta) in Anemic Patients With Chronic Hepatitis C. |
| NCT00560690 | PHASE4 | COMPLETED | The Effect of Adding Metformin to the Treatment of Hepatitis C |
| NCT00575224 | PHASE4 | COMPLETED | Pegasys and Copegus for Asian Patients With Treatment-naive Hepatitis C Genotypes 6, 7, 8, 9 |
| NCT00611819 | PHASE4 | UNKNOWN | Two Different Treatments 24 vs 48 Weeks Chronic Hepatitis C Genotypes 2 and/or 3 in co-Infected HIV-HCV |
| NCT00612755 | PHASE4 | COMPLETED | Efficacy and Safety to Extend Treatment 24 Weeks in co-Infected HIV-HCV Genotype 1 and/or 4 |
| NCT00629967 | PHASE4 | COMPLETED | A Randomized Trial of 24-Week Versus 48-Week Courses of Peginterferon Plus Ribavirin for HCV Genotype-1 Patients |
| NCT00641654 | PHASE4 | TERMINATED | Combination Therapy With Pegylated Interferon and Ribavirin in Patients With Chronic Hepatitis C Genotype 2 or 3 Infection Who Previously Have Relapsed After Therapy With Pegylated Interferon and Ribavirin |
| NCT00686777 | PHASE4 | COMPLETED | Pegylated Interferon (PEG-IFN) Alfa-2b and Low Dose Ribavirin for the Treatment of Chronic Hepatitis C Patients With Genotype 1 High Viral Load and Low Body Weight (Study P05172)(COMPLETED) |
| NCT00800748 | PHASE4 | COMPLETED | A Study of Combination Treatment With Peginterferon Alfa-2a (Pegasys) Plus Ribavirin (Copegus) in Participants With Chronic Hepatitis C |
| NCT00803309 | PHASE4 | TERMINATED | Study to Assess the Efficacy of 12 Versus 24 Weeks of Extended Treatment in HCV-Genotype 2/3 Patients |
| NCT00830609 | PHASE4 | COMPLETED | High Dose Versus Standard Dose of Ribavirin in Patients With Chronic Hepatitis C, Genotype 3 |
| NCT00834860 | PHASE4 | UNKNOWN | Peginterferon Plus Ribavirin for Hepatitis C Patients Concomitant With Hepatocellular Carcinoma |
| NCT00845676 | PHASE4 | COMPLETED | Treatment of Acute Hepatitis C Virus in HIV Co-Infection |
| NCT00887081 | PHASE4 | UNKNOWN | Interferon and Ribavirin Treatment in Patients With Hemoglobinopathies |
| NCT00910975 | PHASE4 | COMPLETED | Individualized Duration of Peg-interferon/Ribavirin Treatment of Hepatitis C |
| NCT00922779 | PHASE4 | COMPLETED | A Study of Ribavirin in Combination With PEGASYS (Peginterferon Alfa-2a (40KD))in Patients With Chronic Hepatitis C |
| NCT00940420 | PHASE4 | COMPLETED | A Study of Combination Treatment With Pegasys (Peginterferon Alfa) and Copegus (Ribavirin)in Patients With Chronic Hepatitis C |
| NCT00948220 | PHASE4 | COMPLETED | Influence of Antiviral Therapy on Bone Mineral Density and Metabolism in Patients With Chronic Hepatitis C |
| NCT00957866 | PHASE4 | COMPLETED | Prospective Anti-Hepatitis C Virus (Anti-HCV) Trial of Peg-Interferon and Ribavirin in Subjects of First Nations, Metis and Caucasian Ethnicity |
| NCT00993122 | PHASE4 | COMPLETED | Ribavirin Pre-treatment Followed by Combined Standard Therapy in Hepatitis C Virus (HCV) Recipients |
| NCT01033448 | PHASE4 | COMPLETED | A Study of Extended Therapy of PEGASYS (Peginterferon Alfa-2a) in Combination With COPEGUS (Ribavirin) in Patients With Chronic Hepatitis C and Slow Response |
| NCT01045278 | PHASE4 | COMPLETED | Hepatitis C in a Cohort of Patients With Maintenance Therapy for Opiate Dependence - Prevalence, Severity and Outcome of Antiviral Therapy |
| NCT01056172 | PHASE4 | UNKNOWN | PegIFN Alfa-2a and RBV for 16 or 24 Weeks in Patients With Chronic Hepatitis C(CHC) 2 With Rapid Virologic Response(RVR) |
| NCT01097395 | PHASE4 | COMPLETED | Concentration-Controlled Ribavirin for the Treatment of Patients With Chronic Hepatitis C Virus Infection |
| NCT01120795 | PHASE4 | COMPLETED | Pegylated Interferon and Ribavirin in Hepatitis C Patients on Opioid Pharmacotherapy |
| NCT01258101 | PHASE4 | COMPLETED | A Study of PEGASYS (Peginterferon Alfa-2a) Plus Ribavirin in Patients With Chronic Hepatitis C (CHC), Genotype 2 or 3 |
| NCT01336010 | PHASE4 | COMPLETED | Treatment of Recently Acquired Hepatitis C Virus Infection |
| NCT01364090 | PHASE4 | COMPLETED | A Collaborative Trial in Injectors of Individualized Treatment for Genotype 2/3 |
| NCT01415141 | PHASE4 | WITHDRAWN | Peginterferon and Ribavirin, With or Without Telaprevir, for Genotype 1 Hepatitis C and IL28B CC Polymorphism |
| NCT01429792 | PHASE4 | COMPLETED | A Study Evaluating Slow Response/Non-Rapid Response in Patients With Chronic Hepatitis C, Genotype 1, 2, 3 & 4 Treated With Pegasys (Peginterferon Alfa-2a) and Copegus (Ribavirin) |
| NCT01443923 | PHASE4 | TERMINATED | Boceprevir Drug Combination for Hepatitis C Treatment in People With and Without HIV |
| NCT01447420 | PHASE4 | COMPLETED | A Study of Sustained Virological Response in Relation to IL28-b Expression in Treatment-Naïve Patients With Chronic Hepatitis C Genotype 1 on Combination Treatment With Pegasys (Peginterferon Alfa-2a) and Copegus (Ribavirin) |
| NCT01467492 | PHASE4 | TERMINATED | Telaprevir, Peg-IFN-alfa-2a, and RBV in Treatment-Experienced Black/African American and Non-Black/African American Subjects With Genotype 1 Chronic Hepatitis C |
| NCT01585324 | PHASE4 | COMPLETED | A Study of The Relationship Between Drop in Hemoglobin and Sustained Virological Response in Patients With Chronic Hepatitis C Treated With Copegus (Ribavirin) and Pegasys (Peginterferon Alfa-2a) |
| NCT01591460 | PHASE4 | COMPLETED | A Triple Combination Therapy Study of Boceprevir, Pegasys and Copegus in Previously Untreated Patients With Genotype 1 Chronic Hepatitis C |
| NCT01592006 | PHASE4 | TERMINATED | Pegylated Interferon, Ribavirin, Telaprevir in Hepatitis C Virus Infection in Orthotopic Liver Transplant Recipients |
| NCT01606800 | PHASE4 | TERMINATED | Efficacy and Safety of Short Course Therapy With Peginterferon Alpha-2b (PEG-IFN Alfa-2b) and Ribavirin (RBV) for Chronic Hepatitis C (Genotype 4) Participants Achieving a Rapid Virological Response at Week 4 of Treatment (MK-8908B-059) |
| NCT01731301 | PHASE4 | UNKNOWN | A Pilot Study to Treat Patients With Chronic Hepatitis C Virus (HCV) Genotype 1 and End-Stage Renal Disease (ESRD) |
| NCT01770483 | PHASE4 | COMPLETED | The Role Of Nitazoxanide, Interferon Alfa And Ribavirin In Treatment Of Hepatitis C Infected Type 2 Diabetic Patients |
| NCT01838772 | PHASE4 | COMPLETED | HCV Treatment in HIV Co-Infected Patients in Asia |
| NCT01841775 | PHASE4 | COMPLETED | Interferon α 2b Pharmacovigilance Study |
| NCT01925183 | PHASE4 | COMPLETED | Individualized Triple-therapy Using Boceprevir in HIV-positive Patients With Hepatitis C |
| NCT01937728 | PHASE4 | COMPLETED | Tailored Regimens of PEGASYS® and Ribavirin for Genotype 1 Chronic Hepatitis C Patients Trial (TARGET-1) |
| NCT02087111 | PHASE4 | COMPLETED | Telaprevir in Genotype 3 HCV |
| NCT02156570 | PHASE4 | COMPLETED | DAA-based Therapy for Recently Acquired Hepatitis C II (DAA = Directly Acting Antiviral) |
| NCT02168361 | PHASE4 | COMPLETED | The SIM-SOF Trial for Hepatitis C |
| NCT02214420 | PHASE4 | COMPLETED | SMV + SOF With/Without RBV for IFN-II Patients With CHC |
| NCT02304159 | PHASE4 | COMPLETED | Study to Evaluate the Safety and Efficacy of Daclatasvir/Sofosbuvir/Ribavirin for 16 Versus 24 Weeks for HCV Genotype 3 Cirrhotics |
| NCT02328651 | PHASE4 | COMPLETED | Effect of Xiaoer Jiebiao Oral Liquid on Hand-foot-mouth Disease |
| NCT02377856 | PHASE4 | COMPLETED | Peginterferon Plus Ribavirin Combination Therapy for Hepatitis C Six Months After Onset of Acute Infection |
| NCT02558114 | PHASE4 | TERMINATED | Ribavirin for Severe Acute and Chronic Hepatitis E Virus Infection. |
| NCT02601976 | PHASE4 | COMPLETED | Evaluation of Unipeg® for Response and Ongoing Safety in Pakistani Population |
| NCT02641379 | PHASE4 | COMPLETED | A Study of Peginterferon Alfa-2a (Pegasys) When Administered in Combination With Ribavirin in Patients With Chronic Hepatitis C (CHC) |
| NCT02717949 | PHASE4 | TERMINATED | Oral Hepatitis C Treatment for Indolent Lymphoma (OPTImaL) Study |
| NCT02761629 | PHASE4 | COMPLETED | Efficacy and Safety of Peg-Interferon Alpha-2a Plus Ribavirin in Genotype 1 Chronic Hepatitis C Participants Co-Infected With Human Immunodeficiency Virus |
| NCT02781649 | PHASE4 | COMPLETED | Exploring Renal Transplants Using Hepatitis C Infected Donors for HCV-negative Recipients |
Clinical evidence (CIViC)
No CIViC predictive evidence (expected for non-precision-medicine drugs).
Pharmacology
Pharmacogenomics
PharmGKB dosing guidelines (2) — CPIC / DPWG genotype-guided dosing for this drug (drug × pharmacogene):
| Guideline | Source | Gene(s) | Dosing | Recommendation |
|---|---|---|---|---|
| Annotation of DPWG Guideline for ribavirin and HLA-B | DPWG | HLA-B | ||
| Annotation of CPIC Guideline for peginterferon alfa-2a, peginterferon | CPIC | IFNL3 | yes |
PharmGKB also curates 46 clinical and 346 variant annotation(s) for this drug (gene-keyed; see PharmGKB).
Related molecules
Related molecules
Molecules sharing ≥1 of this drug’s curated primary targets, merged from two biobtree sources and ranked by shared-target count, then clinical phase: ChEMBL clinical-stage candidates (development phase ≥2) and PubChem drug-class bioactivity (approved / known drugs acting on the target). Deduplicated by drug name; the drug’s own salt forms are excluded. Note: for a drug with few primary targets a shared-target match can reflect off-target / promiscuous binding rather than the same therapeutic mechanism — the phase ordering surfaces bona-fide therapeutics first.
23 molecules share ≥1 primary target. Top 23 by shared-target count:
| Molecule | Source | Status | Shared targets |
|---|---|---|---|
| MYCOPHENOLIC ACID | ChEMBL + PubChem | Phase 4 (approved) | IMPDH1, IMPDH2 |
| MERIMEPODIB | ChEMBL | Phase 2 | IMPDH1, IMPDH2 |
| Adenosine | PubChem | Approved | IMPDH1 |
| Afatinib | PubChem | Approved | IMPDH2 |
| Binimetinib | PubChem | Approved | IMPDH2 |
| Cobimetinib | PubChem | Approved | IMPDH2 |
| Crizotinib | PubChem | Approved | IMPDH2 |
| dacomitinib | PubChem | Approved | IMPDH2 |
| Erlotinib | PubChem | Approved | IMPDH2 |
| Fedratinib | PubChem | Approved | IMPDH2 |
| Fostamatinib | PubChem | Approved | IMPDH2 |
| Gefitinib | PubChem | Approved | IMPDH2 |
| Idelalisib | PubChem | Approved | IMPDH2 |
| Lapatinib | PubChem | Approved | IMPDH2 |
| Nadide | PubChem | Approved | IMPDH1 |
| Pazopanib | PubChem | Approved | IMPDH2 |
| regorafenib | PubChem | Approved | IMPDH2 |
| Selumetinib | PubChem | Approved | IMPDH2 |
| Sorafenib | PubChem | Approved | IMPDH2 |
| Thioguanine | PubChem | Approved | IMPDH1 |
| Tirbanibulin | PubChem | Approved | IMPDH2 |
| Trametinib | PubChem | Approved | IMPDH2 |
| Vorinostat | PubChem | Approved | IMPDH1 |
Related Atlas pages
- Genes: IMPDH1, IMPDH2
- Indicated for: chronic hepatitis C virus infection, cirrhosis of liver, viral infectious disease
- In clinical trials for: hepatitis C virus infection, hepatitis B virus infection, HIV infectious disease, chronic hepatitis B virus infection, respiratory syncytial virus infectious disease, hepatitis, severe acute respiratory syndrome, depressive disorder, acute myeloid leukemia, hepatitis D virus infection, Japanese encephalitis, thrombocytopenia, influenza, Lassa fever, type 1 diabetes mellitus
- Drugs: Mycophenolic Acid, Adenosine, Afatinib, Binimetinib, Cobimetinib, Crizotinib, dacomitinib, Erlotinib, Fedratinib, Fostamatinib, Gefitinib, Idelalisib, Lapatinib, Pazopanib, regorafenib, Selumetinib, Sorafenib, Thioguanine, Tirbanibulin, Trametinib, Vorinostat