Review
Copyright ©The Author(s) 2022.
World J Meta-Anal. Jun 28, 2022; 10(3): 99-121
Published online Jun 28, 2022. doi: 10.13105/wjma.v10.i3.99
Table 1 Approved antivirals for adults and children for chronic hepatitis B
Drug
Adult dosing
Pediatric dosing
Potential side effects
Pregnancy category
Peg-IFN-a-2a (adult) IFN-a-2b (children)180 mcg wkly> 1 yr dose: 6 million IU/m2 three times wklyFlu-like symptoms, fatigue, mood disturbances, cytopenia, autoimmune disorders in adults, anorexia, and weight loss in childrenC
Entecavir0.5 mg daily> 2 yr dose: weight-based to 10-30 kg; above 30 kg: 0.5 mg dailyLactic acidosis (decompensated cirrhosis only)C
Tenofovir dipovoxil fumarate300 daily> 12 yrFanconi syndrome, osteomalacia, lactic acidosisB
Tenofovir alafenamide25 mg daily-Lactic acidosisThere are insufficient human data on use during pregnancy to inform a drug-associated risk of birth defects and miscarriage
Lamivudine100 mg daily2 yr dose: 3 mg/kg daily to max 100 mgPancreatitis lactic acidosisC
Adefovir10 mg daily12 yrAcute renal failure Fanconi syndrome lactic acidosisC
Telbivudine600 mg daily-Creatine kinase elevation and myopathy peripheral neuropathy lactic acidosisB
Table 2 Drugs in pipeline for hepatitis B virus
drug class
Drug
Company
Phase
Core protein inhibitorsAB-506Arbutus Biopharma1
ABI-H0731Assembly Biosciences1,2
ABI-H2158Assembly Biosciences1
EDP-514Enanta Pharmaceuticals1
JNJ-6379Johnson & Johnson1,2
JNJ-0440Johnson & Johnson1
RO7049389Roche1
siRNA, antisense RNAAB-729Arbutus Biopharma1
DCR-HBVSDicerna Pharmaceuticals1
GSK/IONIS-HBV-LRxIonis/GlaxoSmithKline1,2
IONIS-HBVRxIonis/GlaxoSmithKline1,2
JNJ-3989 (ARO-HBV)Johnson & Johnson1,2
RO7062931Roche1
Vir-2218 (ALN-HBV02)Vir Biotechnology/Alnylam1
pol/RT inhibitorTenofovir exalidexContraVir Pharmaceuticals1,2
HBsAg secretion inhibitorsREP-2139Replicor1,2
REP-2165Replicor1,2
HBV entry inhibitorBulevirtideHepatera Ltd1,2
TLR-7 agonistsAL-034Johnson & Johnson/Alios1
RG-7854Roche1
RO7020531Roche1
TLR-8 agonistGS-9688Gilead Sciences1,2
Therapeutic vaccinesAIC-649AiCuris1
INO-1800Inovio Pharmaceuticals1
TG1050Transgene1
RIG-I and NOD2 agonistInarigivirSpring Bank1,2
Apoptosis inducerAPG-1387Ascentage Pharma1
FXR agonistEYP-001Enyo Pharma1,2
Table 3 DAA therapy in pediatric population
Regimen
Patient population
Duration (wk)
Genotype 1
Ledipasvir/sofosbuvirPrior exposure to DAA and IFN (± ribavirin) , no cirrhosis 12
Prior exposure to DAA and IFN (± ribavirin) , compensated cirrhosis24
Glecaprevir/pibrentasviAge ≥ 12 yr or weight ≥ 45 kg with prior exposure to an NS5A inhibitor but no NS3/4A protease inhibitor exposure, no cirrhosis, compensated cirrhosis 16
Age ≥ 12 yr or weighing ≥ 45 kg with prior exposure to NS3/4A protease inhibitors but no NS5A inhibitor exposure, no cirrhosis, compensated cirrhosis 12
Age ≥ 12 yr or weight ≥ 45 kg with prior exposure to an IFN-based regimen (± ribavirin) and/or sofosbuvir but no exposure to NS3/4A or NS5A protease inhibitors, with compensated cirrhosis12
Age ≥ 12 yr or weight ≥ 45 kg with prior exposure to an IFN-based regimen (± ribavirin) and/or sofosbuvir but no exposure to NS3/4A or NS5A protease inhibitors, without cirrhosis8
Genotype 2
Glecaprevir /pibrentasvir Age ≥ 12 yr or weight ≥ 45 kg with prior exposure to an IFN-based regimen (± ribavirin) and/or sofosbuvir but no exposure to NS3/4A or NS5A protease inhibitors, without cirrhosis8
Age ≥ 12 yr or weight ≥ 45 kg with prior exposure to an IFN-based regimen (± ribavirin) and/or sofosbuvir but no exposure to NS3/4A or NS5A protease inhibitors, compensated cirrhosis12
Genotype 3
Glecaprevir/pibrentasvirAge ≥ 12 yr or weight ≥ 45 kg with prior exposure to an IFN-based regimen (± ribavirin) and/or sofosbuvir but no exposure to NS3/4A or NS5A protease inhibitors, no cirrhosis or compensated cirrhosis 16
Genotype 4
Glecaprevir/pibrentasvirAge ≥ 12 yr or weight ≥ 45 kg with prior exposure to an IFN-based regimen (± ribavirin) and/or sofosbuvir but no exposure to NS3/4A or NS5A protease inhibitors, compensated cirrhosis12
Age ≥ 12 yr or weight ≥ 45 kg with prior exposure to an IFN-based regimen (± ribavirin) and/or sofosbuvir but no exposure to NS3/4A or NS5A protease inhibitors, no cirrhosis8
Ledipasvir/sofosbuvirAge ≥ 3 yr with prior exposure to an IFN (± ribavirin) plus an HCV protease inhibitor regimen, no cirrhosis or compensated cirrhosis12
Genotype 5
Ledipasvir/sofosbuvirAge ≥ 3 yr with prior exposure to an IFN (± ribavirin) plus an HCV protease inhibitor regimen, no cirrhosis or compensated cirrhosis 12
Glecaprevir/pibrentasvirAge ≥ 12 yr or weight ≥ 45 kg with prior exposure to an IFN-based regimen (± ribavirin) and/or sofosbuvir but no exposure to NS3/4A or NS5A protease inhibitors, no cirrhosis8
Age ≥ 12 yr or weight ≥ 45 kg with prior exposure to an IFN-based regimen (± ribavirin) and/or sofosbuvir but no exposure to NS3/4A or NS5A protease inhibitors, with compensated cirrhosis12
Genotype 6
Glecaprevir/pibrentasvirAge ≥ 12 yr or weight ≥ 45 kg with prior exposure to an IFN-based regimen (± ribavirin) and/or sofosbuvir but no exposure to NS3/4A or NS5A protease inhibitors, no cirrhosis 8
Age ≥ 12 yr or weight ≥ 45 kg with prior exposure to an IFN-based regimen (± ribavirin) and/or sofosbuvir but no exposure to NS3/4A or NS5A protease inhibitors, with compensated cirrhosis12
Ledipasvir/sofosbuvir Age ≥ 3 yr with prior exposure to an IFN (± ribavirin) plus an HCV protease inhibitor regimen, no cirrhosis, compensated cirrhosis 12
Table 4 DAA therapy for chronic hepatitis C virus
Regimen
Patient population
Duration (wk)
Genotype 1
Daclatasvir + sofosbuvirDecompensated cirrhosis regardless of subtype12
HIV/HCV coinfection when antiretroviral regimen cannot be made to accommodate recommended regimens12
Elbasvir/grazoprevirTreatment naive or Peg/RBV experienced regardless of cirrhosis12
Severe renal impairment (CKD stage 4/5)12
Not for decompensated cirrhosis or post liver transplant with cirrhosis
Glecaprevir/pibrentasvirTreatment naive or Peg/RBV experienced without cirrhosis8
Treatment naive or Peg/RBV experienced with cirrhosis, and non-NS5A failures (including NS3) regardless of cirrhosis12
Post liver transplant without cirrhosis12
Severe renal impairment (CKD stage 4 or 5)8–12
Post kidney transplant regardless of cirrhosis12
Not for decompensated cirrhosis or post liver transplant with cirrhosis
Ledipasvir/sofosbuvirTreatment naive regardless of cirrhosis12
Treatment naive, no cirrhosis, non-black, HIV negative, and HCV RNA <106 IU/mL8
Peg/RBV (± NS3 protease inhibitor) experienced without cirrhosis12
Decompensated cirrhosis, treatment naive or Peg/RBV (± NS3 protease inhibitor) experienced12
Decompensated cirrhosis, prior sofosbuvir failure only24
Post liver transplant regardless of cirrhosis or decompensation12
Post kidney transplant regardless of cirrhosis12
Sofosbuvir/velpatasvirTreatment naive or Peg/RBV ± NS3 protease inhibitor experienced regardless of cirrhosis12
GT1b, non-NS5A DAA experienced regardless of cirrhosis12
Decompensated cirrhosis, treatment naive or Peg/RBV (± NS3 protease inhibitor) experienced12
Decompensated cirrhosis, DAA failure (including NS5A)b24
Sofosbuvir/velpatasvir/voxilaprevirNS5A failures (including NS3 protease inhibitor) regardless of cirrhosis12
GT1a, non-NS5A failures (including NS3 protease inhibitors) regardless of cirrhosis12
Not for decompensated cirrhosis or post liver transplant with cirrhosis
Genotype 2
Daclatasvir + sofosbuvirDecompensated cirrhosis12
Post liver transplant regardless of cirrhosis or decompensation12
Glecaprevir/pibrentasvirTreatment naive or Peg/RBV experienced without cirrhosis8
Treatment naive or Peg/RBV experienced with cirrhosis, and sofosbuvir failures regardless of cirrhosis12
Post liver transplant without cirrhosis12
Severe renal impairment (CKD stage 4 or 5)8–12
Post kidney transplant regardless of cirrhosis12
Not for decompensated cirrhosis or post liver transplant with cirrhosis
Sofosbuvir/velpatasvirTreatment naive, or Peg/RBV or non-NS5A experienced regardless of cirrhosis12
Decompensated cirrhosis, treatment naive or Peg/RBV or non-NS5A experienced12
Decompensated cirrhosis, DAA failure (including sofosbuvir ± NS5A)b24
Post liver transplant with decompensated cirrhosis12
Sofosbuvir/velpatasvir/voxilaprevirNS5A failures12
Not for decompensated cirrhosis or post liver transplant with cirrhosis
Genotype 3
Daclatasvir + sofosbuvirDecompensated cirrhosis12
Post liver transplant regardless of cirrhosis or decompensation12
Glecaprevir/pibrentasvirTreatment naive without cirrhosis8
Treatment naive with compensated cirrhosis12
Post liver transplant without cirrhosis12
Severe renal impairment (CKD stage 4 or 5)8–12
Post kidney transplant regardless of cirrhosis12
Not for decompensated cirrhosis or post liver transplant with cirrhosis
Sofosbuvir + elbasvir/grazoprevirPeg/RBV experienced with compensated cirrhosis12
Not for decompensated cirrhosis or post liver transplant with cirrhosis
Sofosbuvir/velpatasvirTreatment naive without cirrhosis12
Treatment naive with cirrhosis or Peg/RBV experienced without cirrhosis12
Decompensated cirrhosis, treatment naive or Peg/ RBV experienced12
Decompensated cirrhosis, previously exposed to DAA (including sofosbuvir ± NS5A)b24
Post liver transplant with decompensated cirrhosis12
Sofosbuvir/velpatasvir/voxilaprevirPeg/RBV experienced with cirrhosis, or DAA failure (including NS5A inhibitors) regardless of cirrhosis12
Not for decompensated cirrhosis or post liver transplant with cirrhosis
Genotype 4
Daclatasvir + sofosbuvirDecompensated cirrhosis12
HIV/HCV coinfection when antiretroviral regimen cannot be made to accommodate recommended regimens12
Elbasvir/grazoprevirTreatment naive or Peg/RBV experienced with prior relapse, regardless of cirrhosis12
Severe renal impairment (CKD stage 4/5)12
Not for decompensated cirrhosis or post liver transplant with cirrhosis
Glecaprevir/pibrentasvirTreatment naive or Peg/RBV experienced without cirrhosis8
Treatment naive or Peg/RBV experienced with cirrhosis12
Post liver transplant without cirrhosis12
Severe renal impairment (CKD stage 4 or 5)8–12
Post kidney transplant regardless of cirrhosis12
Not for decompensated cirrhosis or post liver transplant with cirrhosis
Treatment naive regardless of cirrhosis or Peg/RBV experienced without cirrhosis12
Decompensated cirrhosis, treatment naive or Peg/ RBV experienced12
Decompensated cirrhosis, sofosbuvir failure24
Post liver transplant regardless of cirrhosis or decompensation12
Post kidney transplant regardless of cirrhosis12
Sofosbuvir/velpatasvirTreatment naive or Peg/RBV experienced regardless of cirrhosis12
Decompensated cirrhosis, treatment naive or Peg/ RBV (± NS3 protease inhibitor) experienced12
Decompensated cirrhosis, DAA failure (including NS5A)24
Sofosbuvir/velpatasvir/voxilaprevirNS5A failures (including NS3 protease inhibitors) regardless of cirrhosis12
Not for decompensated cirrhosis or post liver transplant with cirrhosis
Sofusbuvir/ledipasvirTreatment naive, compensated cirrhosis – not for decompensated cirrhosis12
Genotype 5 or 6
Glecaprevir/pibrentasvirTreatment naive or Peg/RBV experienced without cirrhosis8
Treatment naive or Peg/RBV experienced with cirrhosis12
Post liver transplant without cirrhosis12
Severe renal impairment (CKD stage 4 or 5)8–12
Post kidney transplant regardless of cirrhosis12
Not for decompensated cirrhosis or post liver transplant with cirrhosis
Ledipasvir/sofosbuvirTreatment naive or Peg/RBV experienced regardless of cirrhosis12
Decompensated cirrhosis, treatment naive or Peg/ RBV experienced12
Decompensated cirrhosis, sofosbuvir failure24
Post liver transplant regardless of cirrhosis or decompensation12
Sofosbuvir/velpatasvirTreatment naive or Peg/RBV experienced regardless of cirrhosis12
Decompensated cirrhosis, treatment naive or Peg/RBV (± NS3 protease inhibitor) experienced12
Decompensated cirrhosis, DAA failure (including NS5A)24
Sofosbuvir/velpatasvir/voxilaprevirNS5A failures (including NS3 protease inhibitors) regardless of cirrhosis12
Not for decompensated cirrhosis or post liver transplant with cirrhosis
Table 5 Novel drug treatments for chronic hepatitis D virus
Drug
Mode of action
Administration route
Phase of study
Adverse effect
Myrcludex BInterferes with hepatitis D virus entry into hepatocyteSubcutaneous, daily for 6 moIb, IIaLipase and amylase elevation in phase I but not in phase II study
Through sodium taurocholate cotransporting± pegylated interferon (Peg-IFN)Elevation of taurine- and glycine-conjugated bile acids without apparent clinical consequences
polypeptide inhibitionThrombocytopenia, neutropenia, lymphopenia, and eosinophilia: Generally mild, transient
LonafarnibFarnesyltransferase inhibitor, inhibits virion assemblyOral, 2 to 12 mo, ± ritonavirIIGastrointestinal toxicity (anorexia, nausea with or without vomiting, diarrhea, weight loss): Dose dependent and in lower dose cohorts generally mild and well tolerated
± peg-IFN
Rep-2139-CaNucleic acid polymer, binds with high affinity toIntravenous infusion, once wklyIIHair loss, dysphagia, anorexia, dysgeusia, in hepatitis B study: Related to heavy metal exposure at the trial site
Amphipathic proteins, which are required at variousfor 4-6 mo ± peg-IFNAdministration route-related side effects: peripheral grade 1 hyperemia, fever, chills, and headache
Stages of the viral life cycle