Netupitant

In today's world, Netupitant has gained great relevance in different areas of daily life. From its impact on society to its influence on the global economy, Netupitant has become a topic of discussion and debate that leaves no one indifferent. Throughout history, Netupitant has played a fundamental role in the evolution and development of humanity, marking important milestones and generating significant changes. In this article, we will explore in detail the impact of Netupitant in various areas, analyzing its relevance and contribution to the way we perceive and cope with the world today.

Netupitant
Clinical data
License data
Drug classNK1 receptor antagonists, antiemetics
ATC code
  • None
Pharmacokinetic data
Bioavailability>60% (estimated)
Protein binding>99%
Metabolismmainly CYP3A4; also CYP2D6 and CYP2C9
Elimination half-life88 hours
Excretion71% (faeces)
Identifiers
  • 2--N,2-dimethyl-N-propanamide
CAS Number
PubChem CID
DrugBank
ChemSpider
UNII
KEGG
ChEBI
ChEMBL
CompTox Dashboard (EPA)
Chemical and physical data
FormulaC30H32F6N4O
Molar mass578.603 g·mol−1
3D model (JSmol)
  • Cc1ccccc1c2cc(ncc2N(C)C(=O)C(C)(C)c3cc(cc(c3)C(F)(F)F)C(F)(F)F)N4CCN(CC4)C
  • InChI=1S/C30H32F6N4O/c1-19-8-6-7-9-23(19)24-17-26(40-12-10-38(4)11-13-40)37-18-25(24)39(5)27(41)28(2,3)20-14-21(29(31,32)33)16-22(15-20)30(34,35)36/h6-9,14-18H,10-13H2,1-5H3
  • Key:WAXQNWCZJDTGBU-UHFFFAOYSA-N

Netupitant is an antiemetic medication. In the United States, the combinations of netupitant/palonosetron and the prodrug fosnetupitant/palonosetron (both brand name Akynzeo) are approved by the Food and Drug Administration for the prevention of acute and delayed chemotherapy-induced nausea and vomiting, including highly emetogenic chemotherapy such as with cisplatin.[1][2] In the European Union, the combinations are approved by the European Medicines Agency (EMA) for the same indication.[3][4]

Adverse effects

Side effects of the combination netupitant/palonosetron are similar to palonosetron alone, so that no common side effects can be attributed to netupitant.[3][1]

Interactions

Netupitant blood plasma levels are expected to increase when combined with inhibitors of the liver enzyme CYP3A4 and lowered when combined with inductors of this enzyme.[3]

Being a CYP3A4 inhibitor itself, netupitant could also increase plasma levels of pharmaceuticals that are metabolized by CYP3A4. This effect has been observed with dexamethasone, the anti-cancer drugs docetaxel and etoposide, and to a minor (not clinically significant) extent with levonorgestrel, erythromycin and midazolam.[3]. The clinical relevance of the anti-cancer drug interactions has been questioned.[5]

Pharmacology

Mechanism of action

Netupitant is a selective NK1 receptor antagonist.[6]

Netupitant is a selective neurokinin 1 (NK1) receptor antagonist with potential antiemetic activity. Netupitant competitively binds to and blocks the activity of the human substance P/NK1 receptors in the central nervous system (CNS), thereby inhibiting NK1-receptor binding of the endogenous tachykinin neuropeptide substance P (SP), which may result in the prevention of chemotherapy-induced nausea and vomiting (CINV). SP is found in neurons of vagal afferent fibers innervating the brain-stem nucleus tractus solitarii and the area postrema, which contains the chemoreceptor trigger zone (CTZ), and may be elevated in response to chemotherapy. The NK-receptor is a G-protein receptor coupled to the inositol phosphate signal-transduction pathway and is found in both the nucleus tractus solitarii and the area postrema.[7]

Pharmacokinetics

Bioavailability is estimated to be over 60% for orally taken netupitant. Highest blood plasma concentrations are reached five hours after application. Availability is moderately (10–20%) increased when taken after a fatty meal. Netupitant and its main metabolites (called M1 and M3) are bound to plasma proteins to more than 99%, and M2 protein binding is 97%.[3]

The substance is mainly metabolized by CYP3A4, and to a lesser extent by CYP2D6 and CYP2C9. The main metabolites are desmethyl-netupitant (M1), netupitant N-oxide (M2), and hydroxy-netupitant (M3); all three are pharmacologically active.[3][8]

Netupitant and its metabolites are mainly excreted via the faeces.[3] Biological half-life is 88 hours, significantly longer than that of the first NK1 receptor antagonist, aprepitant, which has a half-life of 9 to 13 hours.[9]

Netupitant metabolites[8]

References

  1. ^ a b "Akynzeo- netupitant and palonosetron capsule Akynzeo- fosnetupitant and palonosetron injection". DailyMed. U.S. National Library of Medicine. 30 April 2018. Archived from the original on 18 October 2020. Retrieved 19 March 2020.
  2. ^ "FDA approves Akynzeo for nausea and vomiting associated with cancer chemotherapy" (Press release). Food and Drug Administration. October 10, 2014. Archived from the original on February 1, 2017. Retrieved December 16, 2019.
  3. ^ a b c d e f g "Akynzeo: Summary of Product Characteristics" (PDF). European Medicines Agency. Archived (PDF) from the original on 26 June 2016. Retrieved 12 July 2016.
  4. ^ "Akynzeo EPAR". European Medicines Agency (EMA). 19 March 2020. Archived from the original on 19 March 2020. Retrieved 19 March 2020.
  5. ^ Natale JJ, Spinelli T, Calcagnile S, Lanzarotti C, Rossi G, Cox D, et al. (June 2016). "Drug-drug interaction profile of components of a fixed combination of netupitant and palonosetron: Review of clinical data". Journal of Oncology Pharmacy Practice. 22 (3): 485–495. doi:10.1177/1078155215586824. PMC 4843089. PMID 25998320.
  6. ^ Rizzi A, Campi B, Camarda V, Molinari S, Cantoreggi S, Regoli D, et al. (September 2012). "In vitro and in vivo pharmacological characterization of the novel NK₁ receptor selective antagonist Netupitant". Peptides. 37 (1): 86–97. doi:10.1016/j.peptides.2012.06.010. PMID 22732666. S2CID 7982557.
  7. ^ "Netupitant". PubChem. U.S. National Library of Medicine. Archived from the original on 2019-01-01. Retrieved 2018-12-31.
  8. ^ a b Spinelli T, Calcagnile S, Giuliano C, Rossi G, Lanzarotti C, Mair S, et al. (January 2014). "Netupitant PET imaging and ADME studies in humans". Journal of Clinical Pharmacology. 54 (1): 97–108. doi:10.1002/jcph.198. PMC 4282341. PMID 24122871.
  9. ^ Haberfeld H, ed. (2015). Austria-Codex (in German). Vienna: Österreichischer Apothekerverlag.
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