Tukysa

Active Ingredient(s): Tucatinib
FDA Approved: * April 17, 2020
Pharm Company: * SEATTLE GENETICS
Category: Cancer

* This drug may consist of multiple approval dates, manufacturers, or distributors. If applicable, they would be listed below under "NDC Database Records".



Tukysa Overview

Tucatinib (INN),[1] sold under the brand name Tukysa, is a small molecule inhibitor of HER2 for the treatment of HER2-positive breast cancer.[2][3] It was developed by Array BioPharma and licensed to Cascadian Therapeutics (formerly Oncothyreon, subsequently part of Seattle Genetics).[4] The recommended tucatinib dose is 300 mg taken orally twice a day in combination with trastuzumab (at standard dosage) and capecitabine (1000 mg...

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Details May Include Instructions, Side Effects, Interactions, Etc. Drug monograph is from Wikipedia. All text is available under the terms of the GFDL (GNU Free Documentation License). Source: en.wikipedia.org/wiki/Tucatinib

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Possible Dosages for this and Related Drugs:

Tucatinib
  • Tablet: 150mg, 50mg
Note: Above list includes dosages for all drugs with the same combination of active ingredients.

NDC Database Records for Tukysa: (2 results)

Sorted by National Drug Code
  • 51144-001 Tukysa 50 mg Oral Tablet by Seattle Genetics, Inc.
  • 51144-002 Tukysa 150 mg Oral Tablet by Seattle Genetics, Inc.

Other drugs which contain Tucatinib or a similar ingredient: (1 result)




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