Peringatan Keamanan

The most commonly reported adverse reactions of all intensity (greater than or equal to 5% in placebo-controlled trials) were fatigue, headache, and nausea FDA Label.

Grazoprevir

DB11575

small molecule approved

Deskripsi

Grazoprevir is a direct acting antiviral medication used as part of combination therapy to treat chronic Hepatitis C, an infectious liver disease caused by infection with Hepatitis C Virus (HCV). HCV is a single-stranded RNA virus that is categorized into nine distinct genotypes, with genotype 1 being the most common in the United States, and affecting 72% of all chronic HCV patients L852. Treatment options for chronic Hepatitis C have advanced significantly since 2011, with the development of Direct Acting Antivirals (DAAs) such as Grazoprevir. Grazoprevir is an inhibitor of NS3/4A, a serine protease enzyme, encoded by HCV genotypes 1 and 4 synthesis. These enzymes are essential for viral replication and serve to cleave the virally encoded polyprotein into mature proteins like NS3, NS4A, NS4B, NS5A and NS5B FDA Label. The barrier for develoment of resistance to NS3/4A inhibitors is lower than that of NS5B inhibitors, another class of DAAs A19593. Subtitutions at amino acid positions 155, 156, or 168 are known to confer resistance. The substitutions of the enzyme's catalytic triad consisting of H58, D82, and S139 are also likely to alter the affinity of the drug for NS3/4A or the activity of the enzyme itself. Despite this disadvantage Grazoprevir is still effective against HCV particularly when paired with DB11574.

In a joint recommendation published in 2016, the American Association for the Study of Liver Diseases (AASLD) and the Infectious Diseases Society of America (IDSA) recommend Grazoprevir as first line therapy in combination with DB11574 for genotypes 1a, 1b, and 4 of Hepatitis C A19593. Grazoprevir and DB11574 are used with or without DB00811 with the intent to cure, or achieve a sustained virologic response (SVR), after 12 weeks of daily therapy. SVR and eradication of HCV infection is associated with significant long-term health benefits including reduced liver-related damage, improved quality of life, reduced incidence of Hepatocellular Carcinoma, and reduced all-cause mortality A19626.

Grazoprevir is available as a fixed dose combination product with DB11574 (tradename Zepatier) used for the treatment of chronic Hepatitis C. Approved in January 2016 by the FDA, Zepatier is indicated for the treatment of HCV genotypes 1 and 4 with or without DB00811 depending on the the presence of resistance associated amino acid substitutions in the NS5A protein and previous treatment failure with DB00811, DB00008, DB00022, or other NS3/4A inhibitors like DB08873, DB06290, or DB05521 FDA Label. When combined together, Grazoprevir and DB11574 as the combination product Zepatier have been shown to achieve a SVR between 94% and 97% for genotype 1 and 97% and 100% for genotype 4 after 12 weeks of treatment L852. It can be used in patients with compensated cirrhosis, human immunodeficiency virus co-infection, or severe kidney disease.

Struktur Molekul 2D

Berat 766.903
Wujud solid

Peta Jejaring Molekuler
Legenda: ObatTargetGenEnzim(Panah → menunjukkan arah efek / relasi)TransporterCarrier

Profil Farmakokinetik

Waktu Paruh (Half-Life) The geometric mean apparent terminal half-life for Grazoprevir is 31 hours in HCV-infected subjects [FDA Label].
Volume Distribusi Grazoprevir has an estimated apparent volume of distribution of 1250 liters [FDA Label]. It is thought to distribute primarily to the liver with its uptake facilitated by organic anion transporting polypeptide 1B1/3.
Klirens (Clearance) The clearance of Grazoprevir has not been determined [FDA Label].

Absorpsi

Grazoprevir reaches peak plasma concentration 0.5-3 hours after administration FDA Label. Grazoprevir has an absolute bioavailability of 27%. When taken with food the peak concentration of Grazoprevir increases 2.8 fold but this increase in exposure has not been deemed clinically relevant.

Metabolisme

Grazoprevir is partially eliminated by oxidative metabolism meditated by CYP3A FDA Label. No circulating metabolites of have been detected in human plasma.

Rute Eliminasi

Grazoprevir is mainly eliminated in the feces (90%) with very little eliminated in the urine (<1%) FDA Label.

Interaksi Makanan

1 Data
  • 1. Take with or without food.

Interaksi Obat

424 Data
Ranolazine The serum concentration of Grazoprevir can be increased when it is combined with Ranolazine.
Lumacaftor The serum concentration of Grazoprevir can be decreased when it is combined with Lumacaftor.
Vemurafenib The serum concentration of Grazoprevir can be increased when it is combined with Vemurafenib.
Apalutamide The serum concentration of Grazoprevir can be decreased when it is combined with Apalutamide.
Cholic Acid The excretion of Grazoprevir can be increased when combined with Cholic Acid.
Pitolisant The serum concentration of Grazoprevir can be decreased when it is combined with Pitolisant.
Isavuconazole The serum concentration of Grazoprevir can be increased when it is combined with Isavuconazole.
Isavuconazonium The serum concentration of Grazoprevir can be increased when it is combined with Isavuconazonium.
Fluconazole The metabolism of Grazoprevir can be decreased when combined with Fluconazole.
Erythromycin The serum concentration of Grazoprevir can be increased when it is combined with Erythromycin.
Reserpine The serum concentration of Grazoprevir can be increased when it is combined with Reserpine.
Sorafenib The serum concentration of Grazoprevir can be increased when it is combined with Sorafenib.
Loxapine The serum concentration of Grazoprevir can be increased when it is combined with Loxapine.
Quinine The serum concentration of Grazoprevir can be increased when it is combined with Quinine.
Toremifene The serum concentration of Grazoprevir can be increased when it is combined with Toremifene.
Verapamil The metabolism of Grazoprevir can be decreased when combined with Verapamil.
Tamoxifen Grazoprevir may decrease the excretion rate of Tamoxifen which could result in a higher serum level.
Mifepristone The serum concentration of Grazoprevir can be increased when it is combined with Mifepristone.
Zonisamide The serum concentration of Grazoprevir can be increased when it is combined with Zonisamide.
Carvedilol The serum concentration of Grazoprevir can be increased when it is combined with Carvedilol.
Propafenone The serum concentration of Grazoprevir can be increased when it is combined with Propafenone.
Lapatinib The serum concentration of Grazoprevir can be increased when it is combined with Lapatinib.
Paliperidone The serum concentration of Grazoprevir can be increased when it is combined with Paliperidone.
Mibefradil The serum concentration of Grazoprevir can be increased when it is combined with Mibefradil.
Biricodar The serum concentration of Grazoprevir can be increased when it is combined with Biricodar.
Elacridar The serum concentration of Grazoprevir can be increased when it is combined with Elacridar.
Flibanserin The serum concentration of Grazoprevir can be increased when it is combined with Flibanserin.
Vandetanib The serum concentration of Grazoprevir can be increased when it is combined with Vandetanib.
Zosuquidar The serum concentration of Grazoprevir can be increased when it is combined with Zosuquidar.
Tariquidar The serum concentration of Grazoprevir can be increased when it is combined with Tariquidar.
Simeprevir The metabolism of Grazoprevir can be decreased when combined with Simeprevir.
Brefeldin A The serum concentration of Grazoprevir can be increased when it is combined with Brefeldin A.
Ivacaftor The serum concentration of Grazoprevir can be increased when it is combined with Ivacaftor.
Crizotinib The serum concentration of Grazoprevir can be increased when it is combined with Crizotinib.
Linagliptin The metabolism of Grazoprevir can be decreased when combined with Linagliptin.
Regorafenib The serum concentration of Grazoprevir can be increased when it is combined with Regorafenib.
Ponatinib Grazoprevir may decrease the excretion rate of Ponatinib which could result in a higher serum level.
Canagliflozin The serum concentration of Grazoprevir can be increased when it is combined with Canagliflozin.
Afatinib Grazoprevir may decrease the excretion rate of Afatinib which could result in a higher serum level.
Ledipasvir The serum concentration of Grazoprevir can be increased when it is combined with Ledipasvir.
Vorapaxar The serum concentration of Grazoprevir can be increased when it is combined with Vorapaxar.
Suvorexant The serum concentration of Grazoprevir can be increased when it is combined with Suvorexant.
Netupitant The metabolism of Grazoprevir can be decreased when combined with Netupitant.
Palbociclib Grazoprevir may decrease the excretion rate of Palbociclib which could result in a higher serum level.
Daclatasvir The serum concentration of Grazoprevir can be increased when it is combined with Daclatasvir.
Niguldipine The serum concentration of Grazoprevir can be increased when it is combined with Niguldipine.
Rolapitant The serum concentration of Grazoprevir can be increased when it is combined with Rolapitant.
Venetoclax The metabolism of Grazoprevir can be decreased when combined with Venetoclax.
Asunaprevir The serum concentration of Grazoprevir can be increased when it is combined with Asunaprevir.
Velpatasvir Grazoprevir may decrease the excretion rate of Velpatasvir which could result in a higher serum level.
Neratinib The serum concentration of Grazoprevir can be increased when it is combined with Neratinib.
Valspodar The serum concentration of Grazoprevir can be increased when it is combined with Valspodar.
Dacomitinib Grazoprevir may decrease the excretion rate of Dacomitinib which could result in a higher serum level.
Glasdegib Grazoprevir may decrease the excretion rate of Glasdegib which could result in a higher serum level.
Voxilaprevir Grazoprevir may decrease the excretion rate of Voxilaprevir which could result in a higher serum level.
Sarecycline The serum concentration of Grazoprevir can be increased when it is combined with Sarecycline.
Rucaparib Grazoprevir may decrease the excretion rate of Rucaparib which could result in a higher serum level.
Laniquidar The serum concentration of Grazoprevir can be increased when it is combined with Laniquidar.
Enasidenib Grazoprevir may decrease the excretion rate of Enasidenib which could result in a higher serum level.
Pibrentasvir Grazoprevir may decrease the excretion rate of Pibrentasvir which could result in a higher serum level.
Glecaprevir Grazoprevir may decrease the excretion rate of Glecaprevir which could result in a higher serum level.
Dexniguldipine The serum concentration of Grazoprevir can be increased when it is combined with Dexniguldipine.
ONT-093 The serum concentration of Grazoprevir can be increased when it is combined with ONT-093.
Ivosidenib The metabolism of Grazoprevir can be increased when combined with Ivosidenib.
Dronedarone The metabolism of Grazoprevir can be decreased when combined with Dronedarone.
Lomitapide The serum concentration of Grazoprevir can be increased when it is combined with Lomitapide.
Entrectinib The serum concentration of Grazoprevir can be increased when it is combined with Entrectinib.
Fedratinib The serum concentration of Grazoprevir can be increased when it is combined with Fedratinib.
Istradefylline The serum concentration of Grazoprevir can be increased when it is combined with Istradefylline.
Norgestimate The serum concentration of Grazoprevir can be increased when it is combined with Norgestimate.
Tacrolimus The serum concentration of Grazoprevir can be increased when it is combined with Tacrolimus.
Carfilzomib The serum concentration of Grazoprevir can be increased when it is combined with Carfilzomib.
Favipiravir The serum concentration of Grazoprevir can be increased when it is combined with Favipiravir.
Methylene blue The serum concentration of Grazoprevir can be increased when it is combined with Methylene blue.
Ripretinib Grazoprevir may decrease the excretion rate of Ripretinib which could result in a higher serum level.
Pralsetinib Grazoprevir may decrease the excretion rate of Pralsetinib which could result in a higher serum level.
Clofazimine The serum concentration of Grazoprevir can be increased when it is combined with Clofazimine.
Arsenic trioxide The serum concentration of Grazoprevir can be increased when it is combined with Arsenic trioxide.
Mefloquine The serum concentration of Grazoprevir can be increased when it is combined with Mefloquine.
Cethromycin The serum concentration of Grazoprevir can be increased when it is combined with Cethromycin.
Ixabepilone The serum concentration of Grazoprevir can be increased when it is combined with Ixabepilone.
Voclosporin The serum concentration of Grazoprevir can be increased when it is combined with Voclosporin.
Eliglustat The serum concentration of Grazoprevir can be increased when it is combined with Eliglustat.
Umbralisib The serum concentration of Grazoprevir can be increased when it is combined with Umbralisib.
Diosmin The serum concentration of Grazoprevir can be increased when it is combined with Diosmin.
Sapropterin The serum concentration of Grazoprevir can be increased when it is combined with Sapropterin.
Levoketoconazole The metabolism of Grazoprevir can be decreased when combined with Levoketoconazole.
Capmatinib The serum concentration of Grazoprevir can be increased when it is combined with Capmatinib.
Belumosudil The serum concentration of Grazoprevir can be increased when it is combined with Belumosudil.
Valsartan The excretion of Grazoprevir can be decreased when combined with Valsartan.
Rosiglitazone The excretion of Grazoprevir can be decreased when combined with Rosiglitazone.
Levocarnitine The excretion of Grazoprevir can be decreased when combined with Levocarnitine.
Sulfasalazine Grazoprevir may decrease the excretion rate of Sulfasalazine which could result in a higher serum level.
Novobiocin The excretion of Grazoprevir can be decreased when combined with Novobiocin.
Ouabain The excretion of Grazoprevir can be decreased when combined with Ouabain.
Rosuvastatin Grazoprevir may decrease the excretion rate of Rosuvastatin which could result in a higher serum level.
Bezafibrate The excretion of Grazoprevir can be decreased when combined with Bezafibrate.
Hyperforin The excretion of Grazoprevir can be decreased when combined with Hyperforin.
Posizolid The excretion of Grazoprevir can be decreased when combined with Posizolid.
Acetylcysteine The excretion of Grazoprevir can be decreased when combined with Acetylcysteine.

Target Protein

Genome polyprotein NS3/4A

Referensi & Sumber

Synthesis reference: Harper S, McCauley JA, Rudd MT, Ferrara M, DiFilippo M, Crescenzi B, Koch U, Petrocchi A, Holloway MK, Butcher JW, Romano JJ, Bush KJ, Gilbert KF, McIntyre CJ, Nguyen KT, Nizi E, Carroll SS, Ludmerer SW, Burlein C, DiMuzio JM, Graham DJ, McHale CM, Stahlhut MW, Olsen DB, Monteagudo E, Cianetti S, Giuliano C, Pucci V, Trainor N, Fandozzi CM, Rowley M, Coleman PJ, Vacca JP, Summa V, Liverton NJ: Discovery of MK-5172, a Macrocyclic Hepatitis C Virus NS3/4a Protease Inhibitor. ACS Med Chem Lett. 2012 Mar 2;3(4):332-6. doi: 10.1021/ml300017p. eCollection 2012 Apr 12.
Artikel (PubMed)
  • PMID: 24666106
    Gentile I, Buonomo AR, Borgia F, Zappulo E, Castaldo G, Borgia G: MK-5172 : a second-generation protease inhibitor for the treatment of hepatitis C virus infection. Expert Opin Investig Drugs. 2014 May;23(5):719-28. doi: 10.1517/13543784.2014.902049. Epub 2014 Mar 26.
  • PMID: 24900473
    Harper S, McCauley JA, Rudd MT, Ferrara M, DiFilippo M, Crescenzi B, Koch U, Petrocchi A, Holloway MK, Butcher JW, Romano JJ, Bush KJ, Gilbert KF, McIntyre CJ, Nguyen KT, Nizi E, Carroll SS, Ludmerer SW, Burlein C, DiMuzio JM, Graham DJ, McHale CM, Stahlhut MW, Olsen DB, Monteagudo E, Cianetti S, Giuliano C, Pucci V, Trainor N, Fandozzi CM, Rowley M, Coleman PJ, Vacca JP, Summa V, Liverton NJ: Discovery of MK-5172, a Macrocyclic Hepatitis C Virus NS3/4a Protease Inhibitor. ACS Med Chem Lett. 2012 Mar 2;3(4):332-6. doi: 10.1021/ml300017p. eCollection 2012 Apr 12.
  • PMID: 22615282
    Summa V, Ludmerer SW, McCauley JA, Fandozzi C, Burlein C, Claudio G, Coleman PJ, Dimuzio JM, Ferrara M, Di Filippo M, Gates AT, Graham DJ, Harper S, Hazuda DJ, Huang Q, McHale C, Monteagudo E, Pucci V, Rowley M, Rudd MT, Soriano A, Stahlhut MW, Vacca JP, Olsen DB, Liverton NJ, Carroll SS: MK-5172, a selective inhibitor of hepatitis C virus NS3/4a protease with broad activity across genotypes and resistant variants. Antimicrob Agents Chemother. 2012 Aug;56(8):4161-7. doi: 10.1128/AAC.00324-12. Epub 2012 May 21.
  • PMID: 28497432
    Bagaglio S, Uberti-Foppa C, Morsica G: Resistance Mechanisms in Hepatitis C Virus: implications for Direct-Acting Antiviral Use. Drugs. 2017 May 12. doi: 10.1007/s40265-017-0753-x.
  • PMID: 25585348
    Myers RP, Shah H, Burak KW, Cooper C, Feld JJ: An update on the management of chronic hepatitis C: 2015 Consensus guidelines from the Canadian Association for the Study of the Liver. Can J Gastroenterol Hepatol. 2015 Jan-Feb;29(1):19-34. Epub 2015 Jan 13.

Contoh Produk & Brand

Produk: 3 • International brands: 0
Produk
  • Zepatier
    Tablet, film coated • - • Oral • US • Approved
  • Zepatier
    Tablet • - • Oral • Canada • Approved
  • Zepatier
    Tablet, film coated • - • Oral • EU • Approved

Sekuens Gen/Protein (FASTA)

Sekuens dimuat saat dibutuhkan agar halaman tetap ringan.
© 2025 Digital Pharmacy Research - Universitas Esa Unggul