simeprevir 🐶 Veterinary Use | Indications/Contra | FAERs-F | FAERs-M | Orange Bk | BioActivity |

Stem definitionDrug idCAS RN
Hepatitis Virus C (HVC) protease inhibitors 4812 923604-59-5

Description:

MoleculeDescription

Molfile Inchi Smiles

Synonyms:

  • olysio
  • TMC-435
  • TMC435350
  • simeprevir
  • simeprevir sodium
Oral HCV-PROTEASE INHIBITOR effective against hepatitis C virus (HCV) serine protease NS3/4A. It is used in the treatment of chronic hepatitis C (Antivirals) genotype 1 infection in adults with compensated liver disease, including CIRRHOSIS.
  • Molecular weight: 749.94
  • Formula: C38H47N5O7S2
  • CLOGP: 5.45
  • LIPINSKI: 3
  • HAC: 12
  • HDO: 2
  • TPSA: 156.89
  • ALOGS: -5.39
  • ROTB: 7

  • Status: OFM

  • Legend:
    OFP - off patent
    OFM - off market
    ONP - on patent

Drug dosage:

DoseUnitRoute
0.15 g O

ADMET properties:

PropertyValueReference
BDDCS (Biopharmaceutical Drug Disposition Classification System) 2 Hosey CM, Chan R, Benet LZ
S (Water solubility) 0.00 mg/mL Bocci G, Oprea TI, Benet LZ

Approvals:

DateAgencyCompanyOrphan
May 14, 2014 EMA
Nov. 22, 2013 FDA JANSSEN PRODS

FDA Adverse Event Reporting System (Female)

MedDRA adverse event termLikelihood ratioLikelihood ratio thresholdPatients taking drug having adverse eventPatients taking drug not having adverse eventPatients not taking drug having adverse eventPatients not taking drug not having adverse event
Platelet count decreased 786.23 38.65 301 4414 115821 63368486
Anaemia 585.05 38.65 325 4390 293105 63191202
White blood cell count decreased 471.06 38.65 221 4494 138883 63345424
Blood bilirubin increased 390.96 38.65 134 4581 37006 63447301
Neutrophil count decreased 278.13 38.65 117 4598 56289 63428018
Haemoglobin decreased 223.50 38.65 137 4578 145348 63338959
Hyperbilirubinaemia 167.78 38.65 53 4662 11261 63473046
Haemolytic anaemia 152.49 38.65 48 4667 10077 63474230
Hepatitis C 113.82 38.65 33 4682 5241 63479066
Hepatocellular carcinoma 111.22 38.65 27 4688 2167 63482140
Pruritus 101.47 38.65 129 4586 361324 63122983
Pyrexia 93.29 38.65 142 4573 470336 63013971
Photosensitivity reaction 86.91 38.65 35 4680 14959 63469348
Off label use 86.90 38.65 168 4547 674294 62810013
Remission not achieved 52.49 38.65 9 4706 122 63484185
Decreased appetite 45.60 38.65 73 4642 250979 63233328
Hepatic failure 45.55 38.65 30 4685 35626 63448681
Hepatic function abnormal 44.43 38.65 30 4685 37112 63447195
Jaundice 43.28 38.65 27 4688 29224 63455083
Hepatic encephalopathy 41.18 38.65 19 4696 11263 63473044
Sunburn 41.04 38.65 13 4702 2775 63481532

FDA Adverse Event Reporting System (Male)

MedDRA adverse event termLikelihood ratioLikelihood ratio thresholdPatients taking drug having adverse eventPatients taking drug not having adverse eventPatients not taking drug having adverse eventPatients not taking drug not having adverse event
Platelet count decreased 553.02 28.77 300 5268 119417 34831946
White blood cell count decreased 397.78 28.77 224 5344 95221 34856142
Blood bilirubin increased 357.83 28.77 156 5412 38140 34913223
Anaemia 313.65 28.77 273 5295 233062 34718301
Hepatitis C 293.26 28.77 94 5474 9736 34941627
Hepatocellular carcinoma 262.22 28.77 81 5487 7428 34943935
Off label use 179.08 28.77 271 5297 419253 34532110
Hyperbilirubinaemia 174.62 28.77 74 5494 16769 34934594
Haemoglobin decreased 150.47 28.77 136 5432 120636 34830727
Neutrophil count decreased 144.78 28.77 94 5474 51010 34900353
Photosensitivity reaction 142.07 28.77 56 5512 10538 34940825
Drug ineffective 88.18 28.77 211 5357 456540 34494823
Jaundice 76.59 28.77 53 5515 31829 34919534
Remission not achieved 71.93 28.77 13 5555 106 34951257
Pruritus 67.36 28.77 97 5471 141884 34809479
Haemolytic anaemia 61.32 28.77 31 5537 10448 34940915
Sunburn 52.50 28.77 17 5551 1806 34949557
Hepatic failure 49.00 28.77 42 5526 34489 34916874
Treatment failure 47.23 28.77 47 5521 46650 34904713
Genotype drug resistance test positive 46.97 28.77 14 5554 1131 34950232
Pyrexia 46.68 28.77 137 5431 332876 34618487
Hepatitis C RNA increased 43.66 28.77 10 5558 285 34951078
Viral load increased 43.35 28.77 16 5552 2511 34948852
Ascites 41.87 28.77 44 5524 46527 34904836
Hepatic encephalopathy 41.44 28.77 27 5541 14658 34936705
Bilirubin conjugated increased 39.34 28.77 16 5552 3255 34948108
Thought blocking 39.15 28.77 8 5560 131 34951232
Rash 35.37 28.77 96 5472 222656 34728707
Choroiditis 33.65 28.77 11 5557 1204 34950159
Hyperuricaemia 33.55 28.77 19 5549 8024 34943339

FDA Adverse Event Reporting System (Geriatric)

MedDRA adverse event termLikelihood ratioLikelihood ratio thresholdPatients taking drug having adverse eventPatients taking drug not having adverse eventPatients not taking drug having adverse eventPatients not taking drug not having adverse event
Platelet count decreased 1387.40 30.73 600 8990 194064 79540734
White blood cell count decreased 909.39 30.73 444 9146 187844 79546954
Anaemia 872.92 30.73 581 9009 444434 79290364
Blood bilirubin increased 700.00 30.73 272 9318 65960 79668838
Neutrophil count decreased 417.07 30.73 210 9380 93749 79641049
Hepatitis C 400.13 30.73 117 9473 11808 79722990
Haemoglobin decreased 377.43 30.73 267 9323 221852 79512946
Hepatocellular carcinoma 372.19 30.73 104 9486 8917 79725881
Hyperbilirubinaemia 320.99 30.73 118 9472 24400 79710398
Haemolytic anaemia 208.42 30.73 79 9511 17741 79717057
Pruritus 152.68 30.73 211 9379 394437 79340361
Photosensitivity reaction 142.01 30.73 63 9527 21064 79713734
Pyrexia 140.18 30.73 273 9317 678436 79056362
Jaundice 113.61 30.73 74 9516 53275 79681523
Remission not achieved 106.26 30.73 21 9569 388 79734410
Hepatic failure 88.51 30.73 67 9523 61145 79673653
Off label use 78.77 30.73 263 9327 906952 78827846
Hepatic encephalopathy 67.86 30.73 40 9550 24126 79710672
Hepatitis C RNA increased 64.94 30.73 14 9576 402 79734396
Bilirubin conjugated increased 62.72 30.73 24 9566 5515 79729283
Rash 60.39 30.73 179 9411 578179 79156619
Pain 58.08 30.73 8 9582 703794 79031004
Hyperuricaemia 56.96 30.73 28 9562 11771 79723027
Ascites 56.87 30.73 57 9533 75505 79659293
Sunburn 55.89 30.73 20 9570 3813 79730985
Decreased appetite 54.23 30.73 124 9466 342294 79392504
Insomnia 48.24 30.73 97 9493 245073 79489725
Malaise 47.66 30.73 148 9442 489721 79245077
Aspartate aminotransferase increased 47.25 30.73 70 9520 138571 79596227
Hepatorenal syndrome 46.64 30.73 18 9572 4231 79730567
Hepatic function abnormal 44.06 30.73 49 9541 73058 79661740
Red blood cell count decreased 42.56 30.73 43 9547 57470 79677328
Viral load increased 37.83 30.73 14 9576 2934 79731864
Hepatic cirrhosis 37.24 30.73 32 9558 34874 79699924
Thought blocking 37.03 30.73 8 9582 232 79734566
Choroiditis 35.30 30.73 11 9579 1370 79733428
Alanine aminotransferase increased 33.96 30.73 66 9524 162504 79572294
Liver disorder 32.85 30.73 42 9548 72375 79662423
Injection site dermatitis 32.29 30.73 5 9585 19 79734779
Incorrect product administration duration 31.40 30.73 19 9571 12003 79722795

FDA Adverse Event Reporting System (Pediatric)

None

Pharmacologic Action:

SourceCodeDescription
ATC J05AP05 ANTIINFECTIVES FOR SYSTEMIC USE
ANTIVIRALS FOR SYSTEMIC USE
DIRECT ACTING ANTIVIRALS
Antivirals for treatment of HCV infections
MeSH PA D000890 Anti-Infective Agents
MeSH PA D000998 Antiviral Agents
MeSH PA D004791 Enzyme Inhibitors
MeSH PA D011480 Protease Inhibitors
FDA MoA N0000182138 Cytochrome P450 1A2 Inhibitors
FDA MoA N0000182141 Cytochrome P450 3A4 Inhibitors
FDA MoA N0000182638 HCV NS3/4A Protease Inhibitors
FDA EPC N0000182639 Hepatitis C Virus NS3/4A Protease Inhibitor
FDA MoA N0000185503 P-Glycoprotein Inhibitors
FDA MoA N0000190107 Organic Anion Transporting Polypeptide 1B1 Inhibitors
FDA MoA N0000190108 Organic Anion Transporting Polypeptide 1B3 Inhibitors
FDA MoA N0000190113 Breast Cancer Resistance Protein Inhibitors
FDA MoA N0000193845 Bile Salt Export Pump Inhibitors
FDA MoA N0000193960 Multidrug Resistance-Associated Protein 2 Inhibitors
FDA MoA N0000193965 Sodium Taurocholate Co-transporting Polypeptide Inhibitors

Drug Use | Suggest Off label Use Form| |View source of the data|

DiseaseRelationSNOMED_IDDOID
Chronic hepatitis C indication 128302006




🐶 Veterinary Drug Use

None

🐶 Veterinary products

None

Acid dissociation constants calculated using MoKa v3.0.0

Dissociation levelDissociation constantType (acidic/basic)
pKa1 4.35 acidic
pKa2 6.66 Basic
pKa3 3.5 Basic

Orange Book patent data (new drug applications)

Formulation strengthTrade nameApplicantApplication numberApproval dateTypeDose formRoutePatent numberPatent expiration datePatent use
EQ 150MG BASE OLYSIO JANSSEN PRODS N205123 Nov. 22, 2013 DISCN CAPSULE ORAL 8349869 July 28, 2026 METHOD OF TREATING HEPATITIS C
EQ 150MG BASE OLYSIO JANSSEN PRODS N205123 Nov. 22, 2013 DISCN CAPSULE ORAL 8741926 July 28, 2026 METHOD OF TREATING HEPATITIS C
EQ 150MG BASE OLYSIO JANSSEN PRODS N205123 Nov. 22, 2013 DISCN CAPSULE ORAL 8754106 July 28, 2026 METHOD OF TREATING HEPATITIS C
EQ 150MG BASE OLYSIO JANSSEN PRODS N205123 Nov. 22, 2013 DISCN CAPSULE ORAL 9040562 July 28, 2026 METHOD OF TREATING HEPATITIS C
EQ 150MG BASE OLYSIO JANSSEN PRODS N205123 Nov. 22, 2013 DISCN CAPSULE ORAL 9353103 July 28, 2026 METHOD OF TREATING HEPATITIS C
EQ 150MG BASE OLYSIO JANSSEN PRODS N205123 Nov. 22, 2013 DISCN CAPSULE ORAL 9623022 July 28, 2026 METHOD OF TREATING HEPATITIS C
EQ 150MG BASE OLYSIO JANSSEN PRODS N205123 Nov. 22, 2013 DISCN CAPSULE ORAL 9856265 July 28, 2026 METHOD OF TREATING HEPATITIS C
EQ 150MG BASE OLYSIO JANSSEN PRODS N205123 Nov. 22, 2013 DISCN CAPSULE ORAL 8148399 Sept. 5, 2029 METHOD OF TREATING HEPATITIS C

Orange Book exclusivity data (new drug applications)

None

Bioactivity Summary:

TargetClassPharosUniProtActionTypeActivity value
(-log[M])
Mechanism
action
Bioact sourceMoA source
Cathepsin S Enzyme IC50 6.10 CHEMBL
Hepatitis C virus serine protease, NS3/NS4A Enzyme INHIBITOR Ki 9.30 CHEMBL CHEMBL
Genome polyprotein Polyprotein INHIBITOR Ki 9.44 SCIENTIFIC LITERATURE DRUG LABEL
Nonstructural protein NS3-4A Unclassified Ki 9.44 CHEMBL
Polyprotein Polyprotein INHIBITOR Ki 9.44 IUPHAR
Genome polyprotein Unclassified Ki 9.30 CHEMBL

External reference:

IDSource
D10081 KEGG_DRUG
4032900 VANDF
CHEBI:134743 CHEBI
30B PDB_CHEM_ID
CHEMBL501849 ChEMBL_ID
7367 IUPHAR_LIGAND_ID
9432 INN_ID
1241946-89-3 SECONDARY_CAS_RN
DB06290 DRUGBANK_ID
9WS5RD66HZ UNII
1482790 RXNORM
207569 MMSL
29896 MMSL
d08182 MMSL
015309 NDDF
015310 NDDF
708823009 SNOMEDCT_US
714167009 SNOMEDCT_US
C2605855 UMLSCUI
D000069616 MESH_DESCRIPTOR_UI
CHEMBL3137358 ChEMBL_ID
24873435 PUBCHEM_CID

Pharmaceutical products:

None