Ripretinib, sold under the brand name Qinlock, is an oral medication used to treat advanced gastrointestinal stromal tumors in adults. It works as a tyrosine kinase inhibitor that blocks the activity of the KIT and PDGFRA kinases, proteins whose mutated forms drive the growth of these tumors. It is indicated as a fourth-line treatment for patients who have already received at least three prior kinase inhibitor therapies, including imatinib. The United States Food and Drug Administration approved ripretinib in May 2020, describing it as the first drug specifically approved in the United States as a fourth-line treatment for advanced gastrointestinal stromal tumor. Australia approved it in July 2020 and the European Union in November 2021. It is developed and marketed by Deciphera Pharmaceuticals, Inc.
Facts
Classification
Approval Status ATC ClassSourced to the subject's own accountL: Antineoplastic and Immunomodulating Agents 2 Route of Administration First Approved / Isolated Year Connections
Sources
1. Ripretinib (Wikipedia)
https://en.wikipedia.org/wiki/Ripretinib, lead section
that originates in the gastrointestinal tract. It is taken by mouth. Ripretinib inhibits the activity of the kinases KIT and PDGFRA, which helps keep cancer cells from growing.
Lead section, approval-status statement
Ripretinib was approved for medical use in the United States in May 2020, in Australia in July 2020, and in the European Union in November 2021.
View the Source2. Anatomical Therapeutic Chemical Classification System (Wikipedia)
WikipediaFirst-level anatomical group codes, Code LQuote, First-level anatomical group codes, Code L
Antineoplastic and immunomodulating agents
View the Source 3. Wikipedia
Wikipedia contributors, Wikimedia Foundation
4. Drugs.com: Qinlock (ripretinib) FDA Approval History
FDA Approval HistoryQuote, FDA Approval History
Qinlock (ripretinib) was first approved by the FDA on May 15, 2020
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