DISCOVERY
Discovery Research
Development
Agriculture
Academic Licensing
Glossary

 

We are committed to developing innovative therapies that have the potential to significantly improve patient outcomes for cancer and other serious diseases. We are building a portfolio of compounds that have first-in-class and best-in-class potential through our own discovery research and clinical development initiatives. We believe that our ability to commercialize novel therapies requires building a critical mass of resources – personnel, technology, intellectual property, and capital – at each step of the drug development process.

Discovery Research

We have extensive expertise and experience modifying gene function in vitro and in vivo as a result of our work on model organisms for the discovery of novel targets and pathways relevant to human disease. Our target discovery platform integrates high-throughput gene knockdown capabilities with cutting-edge cell biology, bioinformatics and protein biochemistry to identify and prioritize targets amenable to small molecule drug discovery. Our current research efforts are focused in the areas of cancer and metabolic diseases; however the platform can be leveraged to identify targets and compounds with applications in other therapeutic areas such as inflammation. For key disease targets that are best addressed by therapeutic antibodies, Exelixis has utilized strategic alliances, combining our biology and screening expertise with antibody discovery and development capabilities of professional antibody companies. This approach enables us to efficiently and comprehensively evaluate the therapeutic potential of biotherapeutics directed to an entire family of receptors and ligands.

We have made significant investments in our discovery operations that support extensive preclinical analyses and optimization, to enhance our potential for success in the clinic. Our discovery operation has the infrastructure and expertise to screen and optimize large numbers of compounds very rapidly while retaining stringent selection criteria. Our ability to optimize lead compounds in a parallel fashion creates a pool of extensively qualified candidates from which we can select the few that meet our high standards for pre-clinical safety, bioavailability, potency, specificity and efficacy. This is achieved by integrating highly automated empirical approaches (high-throughput screening and high-speed chemistry) and data-intensive, structure-assisted design paradigms with extensive pharmacological characterization. We believe the process we created is a new paradigm for consistently discovering novel therapeutic compounds.