by LUC » Thu Oct 23, 2008 9:56 am
Hi Charles,
To answer your question the govt. does license technology that it has developed and discovered through the NIH Office of Technology Transfer (OTT). At this point the the discovery is at the "proof of concept" stage. Meaning, that the technology has been developed in the lab, but has not been through the commercialization process. Once you reached the commercialization process for a newly discovered therapeutic is when costs escalate and you need a different different type of expertise than those who work in basic research at NIH. The govt. doesn't have the infrastructure or experience to develop a manufacturing process, scale-up that process for tox studies, clinical trials (clinical manufacturing) and commercial manufacturing. It however, provides support for clinical trials (e.g., NIH Clinical Trial Planning Grant Program) and grants for start-up biotech companies.
Drug discovery and development is very expensive; of all compounds investigated for use in humans only a small fraction are eventually approved in most nations by government appointed medical institutions or boards, who have to approve new drugs before they can be marketed in those countries. Each year, only about 25 truly novel drugs (New chemical entities) are approved for marketing. This approval comes only after heavy investment in pre-clinical development and clinical trials, as well as a commitment to ongoing safety monitoring. Drugs which fail part-way through this process often incur large costs, while generating no revenue in return. If the cost of these failed drugs is taken into account, the cost of developing a successful new drug (New chemical entity or NCE), has been estimated at about 1 billion USD (not including marketing expenses). A study by the consulting firm Bain & Company reported that the cost for discovering, developing and launching (which factored in marketing and other business expenses) a new drug (along with the prospective drugs that fail) rose over a five year period to nearly $1.7 billion in 2003.
Recently biotech and pharma companies have been looking to streamline the commercialization process to reduce these cuts. Here are two examples: 1) pharma companies have instituted high-throughput screening to discover new NCE's. 2) Biotech's,such as my former company, are developing a platform manufacturing process for clinical and commercial manufacturing to reduce costs associated with complex biotech manufacturing.
Currently pharma is going through industry wide shakeout. Most major pharmas are laying off people in sales (and other areas) to reduce their expenditures and are having a tough time with approving new drugs because their industry is based on a older technology (small-molecules targeted to receptors). They are not structured culturally or physically to incorporate the newer biotechnologies. In the future companies will be smaller, companies will outsource their development/manufacturing and more cross-partnering will occur between companies to commercialize new discoveries.