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Discovery and development of sorafenib: a multikinase inhibitor for treating cancer

Nature Reviews Drug Discovery · 2006 · Vol. 5(10) · pp. 835–844
Scott M. WilhelmChristopher CarterMark LynchTimothy B. LowingerJacques DumasRoger A. SmithBrian SchwartzRonit SimantovSusan L. Kelley

Abstract

Since the molecular revolution of the 1980s, knowledge of the aetiology of cancer has increased considerably, which has led to the discovery and development of targeted therapies tailored to inhibit cancer-specific pathways. The introduction and refinement of rapid, high-throughput screening technologies over the past decade has greatly facilitated this targeted discovery and development process. Here, we describe the discovery and continuing development of sorafenib (previously known as BAY 43-9006), the first oral multikinase inhibitor that targets Raf and affects tumour signalling and the tumour vasculature. The discovery cycle of sorafenib (Nexavar; Bayer Pharmaceuticals) - from initial screening for a lead compound to FDA approval for the treatment of advanced renal cell carcinoma in December 2005 - was completed in just 11 years, with approval being received approximately 5 years after the initiation of the first Phase I trial.

Cancer Mechanisms and TherapyMelanoma and MAPK PathwaysPI3K/AKT/mTOR signaling in cancerSorafenibDrug discoveryMedicineCancerDrug developmentKinaseClinical trialPharmacologyOncologyCancer research

MeSH terms

SorafenibAnimalsAntineoplastic AgentsBenzenesulfonatesCarcinoma, Renal CellClinical Trials as TopicHumansKidney NeoplasmsNeoplasmsNiacinamidePhenylurea CompoundsPyridinesDrug DesignCombinatorial Chemistry TechniquesReceptors, Vascular Endothelial Growth Factor
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Discovery and development of sorafenib: a multikinase inhibitor for treating cancer
Nature Reviews Drug Discovery · 2006 · 1,812 citations
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