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Commentary
Nature Biotechnology  15, 1318 - 1319 (1997)
doi:10.1038/nbt1297-1318

Drug Development: The role of innovation in drug development

Jürgen Drews1 & Stefan Ryser1

1Jürgen Drews is president of global research and Stefan Ryser is chief of international research staff, Hoffmann-La Roche, CH-4002 Basel, Switzerland (stefan.ryser@roche.com).


REFERENCES
  1. Human disease—From genetic causes to biochemical effects. Proceedings of the Roche Symposium "The Genetic Basis of Human Disease", October 2−3, 1996, Basel. Drews, J. and Ryser, S. (eds.) Ex Libris Roche 9. Blackwell Science, Berlin.
  2. Lifton, R. Human disease—From genetic causes to biochemical effects. Proceedings of the Roche Symposium "The Genetic Basis of Human Disease", October 2−3, 1996, Basel. Drews, J. and Ryser, S. (eds.) Ex Libris Roche 9. Blackwell Science, Berlin.
  3. Weber, W. 1997. pp. 10−11 in Pharmacogenetics. Oxford Univ. Press, New York and Oxford.
  4. Ohsako, S. and Deguchi, T. 1990. J. Biol. Chem. 265: 4630−4634. | PubMed  | ISI | ChemPort |
  5. Weber, W. 1997. pp. 12−13 in Pharmacogenetics. Oxford Univ. Press, New York and Oxford.
  6. Mossinghoff, G.J. 1995. Drug Info. J. 29: 1077−1090.
  7. Drews, J. and Ryser, S. 1997. Drug Discovery Today 2: 365−372. | Article | ISI |
  8. It is obvious that these constraints are entirely dependent on a set of financial assumptions relating to costs, sales and discount rates for R&D expenditures. If these assumptions are modified, if for instance the discount rates after launch are lowered from 14% to 8% or if only out of pocket expenses are taken into account and opportunity costs altogether neglected, the picture brightens considerably. Eventually, such changes may have to be made.
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ISSN: 1087-0156
EISSN: 1546-1696
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