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TECHNOLOGY FORESIGHT SUMMIT - Unido

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Part two. Biotechnology Forum 65<br />

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In silico ADME-Tox tools and electronic databases to profile and prioritize<br />

compounds earlier in the drug discovery process<br />

The use of structural similarities and differences of protein target and<br />

anti-targets to design highly specific drugs and examples of virtual<br />

screening to identify small drug-like molecules able to mimic or modulate<br />

the biological activity of complex biomolecules<br />

Pharmacogenomics to study how genetic variation influences individual<br />

responses to a drug<br />

In silico R&D methods to support drug development for Rheumatoid<br />

Arthritis (RA). A mathematical model is developed to stimulate the<br />

clinical symptoms and drug response of a virtual RA patient.<br />

The starting point of the last speaker, Prof. Laszlo Takacs (Pfizer, France):<br />

“Parallel Biology: Current Aspects of Genome Research and its Application in<br />

the Pharmaceutical Industry” was the comparison of hypothesis-driven research<br />

with the hypothesis-free, encyclopaedic, data-collecting work which is the<br />

ruling trend in pharmaceutical research today. He emphasized the importance<br />

of the integration of the two approaches in what he called “parallel<br />

biology”. This integration means that the functional analysis of single genes<br />

must go hand-in-hand with data-mining and comparison of huge data-sets,<br />

using sophisticated computational tools. He gave a brief historic overview of<br />

how these two approaches developed lately in both fundamental (academic)<br />

and applied (pharmaceutical) research. He offered a rather pessimistic view<br />

on various problems faced by the pharmaceutical industry (diminishing value<br />

of patents, hostile environment, diminishing returns on increasing investments).<br />

The perspectives of genomic research for drug discovery and development<br />

were highly overestimated, they created false expectations for “magic<br />

bullets” and “miracle cures” and so far none of these have been realized.<br />

In the last part of his contribution he discussed the possibilities open for<br />

the CEE countries in this field. Academic excellence is available in this region,<br />

but capital investment for large-scale projects is missing. Therefore it is necessary<br />

to find those “ecological niches” where brilliant ideas can result in<br />

useful leads to be developed in cooperation with large companies.<br />

The discussion was centred around the problems of patenting. Three<br />

problematic aspects of patenting were mentioned: (a) the question of patenting<br />

living organisms or genes; (b) the differences between the principles of<br />

patenting in the US and in the EU; (c) the lack of motivation and skills, and<br />

money required for successful patent applications by academic scientists,<br />

especially in the CEE and NIS regions.

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