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Drugs and Medicinal Substances

Tucatinib

Antineoplastic and Immunomodulating Agents

Tucatinib, sold under the brand name Tukysa, is an anticancer medication used to treat HER2 positive breast cancer. It works as a small molecule inhibitor of HER2, blocking the enzyme that drives the growth of these cancer cells. Developed by Array BioPharma, it is taken orally, usually in combination with other therapies. The drug received United States approval in April 2020, followed by approval in Australia in August 2020 and in the European Union in February 2021.

Facts
Drug Class
Small molecule HER2 kinase inhibitor 1
Mechanism of Action
Blocks the HER2 kinase enzyme, preventing HER2-positive cancer cells from growing 1
Approved Use
Indicated with trastuzumab and capecitabine for advanced unresectable or metastatic HER2-positive breast cancer 1
First Approved / Isolated Year
2020 1
Significant Risk
Common side effects include diarrhea, palmar-plantar erythrodysesthesia, nausea, fatigue, hepatotoxicity, vomiting and stomatitis 1
Classification
Approval Status
Approved 1
ATC ClassSourced to the subject's own account
L: Antineoplastic and Immunomodulating Agents 2
Route of Administration
Oral 3
Connections

Long-Form Articles

Sources
1. Tucatinib (Wikipedia)
  • Lead section
    Small molecule inhibitor of HER2
  • History section
    Kinase inhibitor meaning it blocks a type of enzyme (kinase) and helps prevent the cancer cells from growing
  • Medical uses section
    Indicated in combination with trastuzumab and capecitabine for the treatment of adults with advanced unresectable or metastatic HER2-positive breast cancer
  • History section, FDA approval sentence
    In April 2020, the U.S. Food and Drug Administration (FDA) approved tucatinib
  • Lead section, side effects sentence
    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)
  • Lead section, approval-status statement
    Tucatinib was approved for medical use in the United States in April 2020, in Australia in August 2020, and in the European Union in February 2021.
View the Source
2. Anatomical Therapeutic Chemical Classification System (Wikipedia)
WikipediaFirst-level anatomical group codes, Code L
Quote, First-level anatomical group codes, Code L
Antineoplastic and immunomodulating agents
View the Source
3. Tucatinib (Wikipedia)
WikipediaInfobox drug, routes_of_administration
Quote, Infobox drug, routes_of_administration
By mouth
View the Source
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