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Tucatinib information


Tucatinib
Clinical data
Pronunciation/tuˈkætɪnɪb/
too-KAT-in-ib
Trade namesTukysa
Other namesONT-380, ARRY-380
AHFS/Drugs.comMonograph
MedlinePlusa620032
License data
  • US DailyMed: Tucatinib
Pregnancy
category
  • AU: D[1]
Routes of
administration
By mouth
ATC code
  • L01EH03 (WHO)
Legal status
Legal status
  • AU: S4 (Prescription only)
  • CA: ℞-only[2]
  • US: ℞-only[3]
  • EU: Rx-only[4][5]
Identifiers
CAS Number
  • 937263-43-9
PubChem CID
  • 51039094
DrugBank
  • DB11652
ChemSpider
  • 34995558
UNII
  • 234248D0HH
KEGG
  • D11141
ChEMBL
  • ChEMBL3989868
Chemical and physical data
FormulaC26H24N8O2
Molar mass480.532 g·mol−1
3D model (JSmol)
  • Interactive image
SMILES
  • Cc1cc(Nc2ncnc3ccc(NC4=NC(C)(C)CO4)cc23)ccc1Oc1ccn2ncnc2c1
InChI
  • InChI=1S/C26H24N8O2/c1-16-10-17(5-7-22(16)36-19-8-9-34-23(12-19)28-15-30-34)31-24-20-11-18(4-6-21(20)27-14-29-24)32-25-33-26(2,3)13-35-25/h4-12,14-15H,13H2,1-3H3,(H,32,33)(H,27,29,31)
  • Key:SDEAXTCZPQIFQM-UHFFFAOYSA-N

Tucatinib, sold under the brand name Tukysa, is an anticancer medication used for the treatment of HER2-positive breast cancer.[3][4] It is a small molecule inhibitor of HER2.[6][7] It was developed by Array BioPharma and licensed to Cascadian Therapeutics (formerly Oncothyreon, subsequently part of Seattle Genetics).[8]

Common side effects include diarrhea, palmar-plantar erythrodysesthesia (burning or tingling discomfort in the hands and feet), nausea, fatigue, hepatotoxicity (liver damage), vomiting, stomatitis (inflammation of the mouth and lips), decreased appetite, abdominal pain, headache, anemia and rash.[9][10] Tucatinib may cause harm to a developing fetus or baby.[9]

Tucatinib was approved for medical use in the United States in April 2020,[9][10][11] in Australia in August 2020,[1] and in the European Union in February 2021.[4]

  1. ^ a b "Tukysa". Therapeutic Goods Administration (TGA). 21 August 2020. Archived from the original on 1 October 2020. Retrieved 22 September 2020.
  2. ^ "Summary Basis of Decision (SBD) for Tukysa". Health Canada. 23 October 2014. Archived from the original on 30 May 2022. Retrieved 29 May 2022.
  3. ^ a b Cite error: The named reference Tukysa FDA label was invoked but never defined (see the help page).
  4. ^ a b c "Tukysa EPAR". European Medicines Agency (EMA). 9 December 2020. Archived from the original on 22 March 2021. Retrieved 18 February 2021. Text was copied from this source which is © European Medicines Agency. Reproduction is authorized provided the source is acknowledged.
  5. ^ "Tukysa Product information". Union Register of medicinal products. Retrieved 3 March 2023.
  6. ^ "ONT-380 Active Against CNS Mets in HER2-Positive Breast Cancer". Cancer Network. 15 December 2015. Retrieved 17 April 2020.[permanent dead link]
  7. ^ Martin M, López-Tarruella S (October 2018). "Emerging Therapeutic Options for HER2-Positive Breast Cancer". American Society of Clinical Oncology Educational Book. American Society of Clinical Oncology. Annual Meeting. 35 (36): e64–70. doi:10.1200/EDBK_159167. PMID 27249772.
  8. ^ "Tucatinib" (PDF). Statement on a Nonproprietary Name Adopted by the USAN Council. Archived (PDF) from the original on 27 August 2021. Retrieved 31 January 2017.
  9. ^ a b c Cite error: The named reference FDA Tukysa PR was invoked but never defined (see the help page).
  10. ^ a b Cite error: The named reference FDA approval was invoked but never defined (see the help page).
  11. ^ Cite error: The named reference FDA Drug Approval Package was invoked but never defined (see the help page).

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