Table 1.
|
Compound
|
Class and action
|
Phase of development
|
Ref. or trial number
|
Entry Inhibitors | HBIG | Polyclonal antibodies neutralizing HBsAg | Available | Herrscher et al[29] |
GC1102 | Monoclonal antibody neutralizing HBsAg | Phase II | NCT03801798 | |
HzKR359-1, HzKR127-3.2 | Anti-preS1 monoclonal antibodies | Preclinical | Wi et al[30] | |
Heparin, Suramin | Inhibition of HBV-HSPGs interaction | Preclinical | Herrscher et al[29] and Petcu et al[33] | |
SALPs | Inhibition of HBV-HSPGs interaction | Preclinical | Krepstakies et al[32] | |
PAC and analogs | Anti-preS1 oligomeric flavonoid analogs | Preclinical | Tsukuda et al[35] | |
Conjugated bile acids (TCA, UDCA, TUDCA) | NTCP inhibitors | Preclinical | Yan et al[36] | |
Ezetimibe, Irbesartan | NTCP inhibitors | Available | Lucifora et al[37] and Ko et al[38] | |
Cyclosporine A analogs (SCY450, SCY995) | NTCP inhibitors | Preclinical | Watashi et al[39] and Shimura et al[40] | |
Bulevirtide(Myrcludex B) | NTCP inhibitor | Phase III | Wedemeyer et al[41] | |
TargetingcccDNA | Interferons, TNF-α, Lymphotoxin-β receptor agonists | cccDNA degradation | Available | Bockmann et al[44] and Xia et al[45] |
ccc-R08 | cccDNA destabilizer | Preclinical | Wang et al[46] | |
Zinc finger nucleases | Gene editing technology | Preclinical | Cradick et al[47] | |
TALENs | Gene editing technology | Preclinical | Chen et al[49] | |
CRISPR‐associated (Cas) nucleases | Gene editing technology | Preclinical | Ramanan et al[48], Seeger and Sohn[50], and Martinez et al[51] | |
C646 | CBP and p300 inhibitorEpigenetic silencing | Preclinical | Cougot et al[54] | |
GS-5801 | Lysine demethylase 5 inhibitorEpigenetic silencing | Phase I | Gilmore et al[55] | |
EYP001 | FXR agonist | Phase II | Erken et al[56] | |
TargetingHBx | Nitazoxide | HBx-DDB1 interaction inhibitor | Phase II | Sekiba et al[58], Rossignol and Bréchot[59] |
Pevonedistat | NEDD8-activating enzyme inhibitor | Preclinical | Sekiba et al[60] | |
AGK2 | SIRT-2 inhibitor | Preclinical | Yu et al[61] | |
CRV431 | Cyclophilin inhibitor | Phase I | NCT03596697 | |
RNA interference | JNJ-3989 | siRNA | Phase II | Gane et al[66] |
VIR-2218 (or ALN-HBV) | siRNA | Phase II | Gane et al[67] | |
ARB-1467 | siRNA | Phase II | Streinu-Cerce et al[68] | |
ARB-1740 | siRNA | Phase I | Thi et al[191] | |
AB-729 | siRNA | Phase I | Yuen et al[69] | |
RG6346 (or DCR-HBVS) | siRNA | Phase II | Yuen et al[70] | |
GSK3228836, GSK33389404 | ASOs | Phase II | Han et al[71] and Yuen et al[72] | |
ALG-020572, ALG-020576 | ASOs | Preclinical | Hong et al[74] | |
RO7062931 (or RG6004) | Antisense LNA | Phase I | Yuen et al[75] | |
Gapmers | Antisense LNA | Preclinical | Cortese et al[76] | |
RG7834 | RNA destabilizer | Preclinical | Mueller et al[77] and Zhou et al[78] | |
Core protein allosteric modulators (CpAMs) | RO7049389 (or RG7907) | Class I CpAM (HAP derivative) | Phase II | Gane et al[82] |
GLS4 (or morphothiadine) | Class I CpAM (HAP derivative) | Phase II | Zhao et al[83] | |
KL060332 | Class I CpAM (HAP derivative) | Phase I | Tai et al[84] | |
NVR3-778 | Class II CpAM (SBA derivative) | Phase I | Yuen et al[85] | |
JNJ-6379 | Class II CpAM (SBA derivative) | Phase II | Berke et al[86] and Janssen et al[87] | |
AB-423 | Class II CpAM (SBA derivative) | Phase I | Mani et al[192] | |
EDP-514 | Class II CpAM | Phase I | NCT04470388 | |
ABI-H0731 | CpAM | Phase II | Fung et al[88] and Yuen et al[89] | |
ABI-H2158 | CpAM | Phase II | Agarwal et al[90] | |
ABI-H3733 | CpAM | Phase I | NCT04271592 | |
QL-007 | CpAM | Phase I | NCT03770624 | |
ZM-H1505R | CpAM (Pyrazole derivative) | Phase I | NCT04220801 | |
ALG-001075, ALG-000184 | Class II CpAMs | Preclinical | Zhang et al[193] | |
GLP-26 | Class II CpAM (SBA derivative) | Preclinical | Amblard et al[194] | |
AT-61, AT-130 | Class II CpAMs (PPA derivatives) | Preclinical | Delaney et al[195] | |
Phthalazinone derivatives | CpAMs | Preclinical | Chen et al[196] | |
HBsAg inhibitors | REP 2139, REP 2156 | NAPsSVP release inhibitors | Phase II | Bazinet et al[95] |
ALG-010133 | STOPS | Phase I | Nie et al[94] and Gohil et al[96] |
ASOs: Antisense oligonucleotides; CBP: CREB binding protein; cccDNA: Covalently closed circular DNA; CpAM: Core protein allosteric modulators; DDB1: DNA damage-binding protein 1; FXR: Farnesoid X receptor; HAP: Heteroaryldihydropyrimidine; HBIG: Hepatitis B immunoglobulin; HBsAg: Hepatitis B surface antigen; HBV: Hepatitis B virus; HBx: Hepatitis B virus X protein; HSPGs: Heparan sulfate proteoglycans; LNA: Locked nucleic acid; NEDD8: Neural precursor cell expressed, developmentally downregulated-regulated 8; NTCP: Na+ - taurocholate cotransporting polypeptide; PAC: Proanthocyanidins; PPA: Phenylpropenamide; SALPs: Synthetic anti-lipopolysaccharide peptides; SBA: Sulfamoylbenzamide; siRNA: Small interfering RNA; SIRT-2: Sirtuin 2; STOPS: S-antigen transport inhibitory oligonucleotide polymers; SVP: Subviral particles; TALENs: Transcription activator-like effector nucleases; TCA: Taurocholic acid; TUDCA: Tauroursodeoxycholic acid; UDCA: Ursodeoxycholic acid.