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

Article Details

Citation

Wilhelm S, Carter C, Lynch M, Lowinger T, Dumas J, Smith RA, Schwartz B, Simantov R, Kelley S

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

Nat Rev Drug Discov. 2006 Oct;5(10):835-44.

PubMed ID
17016424 [ View in PubMed
]
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.

DrugBank Data that Cites this Article

Drug Targets
DrugTargetKindOrganismPharmacological ActionActions
SorafenibFibroblast growth factor receptor 1ProteinHumans
Yes
Inhibitor
Details
SorafenibProto-oncogene tyrosine-protein kinase receptor RetProteinHumans
Yes
Inhibitor
Details
SorafenibVascular endothelial growth factor receptor 1ProteinHumans
Yes
Inhibitor
Details