Tivozanib is an oral cancer drug sold under the brand name Fotivda that belongs to the tyrosine kinase inhibitor family. Chemically a quinoline urea derivative, it suppresses angiogenesis, the growth of new blood vessels that tumors need to expand, by inhibiting all three vascular endothelial growth factor receptors rather than just one. It was approved in the European Union in August 2017 and later by the United States Food and Drug Administration in March 2021, both times for advanced renal cell carcinoma, the most common form of kidney cancer, specifically for patients whose disease had progressed after at least two earlier systemic therapies. Tivozanib is taken as a capsule by mouth. In clinical trials, common side effects included high blood pressure in roughly half of patients, voice changes, fatigue and diarrhea each in about a quarter of patients, along with reduced appetite, nausea, low thyroid hormone, cough and mouth inflammation.
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. Tivozanib (Wikipedia)
Lead section, approval-status statementQuote, Lead section, approval-status statement
Tivozanib was approved for medical use in the European Union in August 2017, and in the United States in March 2021.
View the Source 2. 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. Tivozanib (Wikipedia)
WikipediaInfobox drug, routes_of_administrationQuote, Infobox drug, routes_of_administration
By mouth
View the Source 4. Drugs.com: Fotivda (tivozanib) FDA Approval History
FDA Approval HistoryQuote, FDA Approval History
Fotivda (tivozanib) received FDA approval on March 10, 2021
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