Skip to main content

Thank you for visiting nature.com. You are using a browser version with limited support for CSS. To obtain the best experience, we recommend you use a more up to date browser (or turn off compatibility mode in Internet Explorer). In the meantime, to ensure continued support, we are displaying the site without styles and JavaScript.

  • Opinion
  • Published:

Developing drug prototypes: pharmacology replaces safety and tolerability?

Abstract

New medicines are designed to bind to receptors or enzymes and are tested in animal cells, tissues and whole organisms in a highly scientific process. Subsequently they are often administered to human subjects with tolerability as the primary objective. The process of development is considered to be linear and consecutive and passes through the famous four phases of development (Phase Iā€“ Phase IV). This is efficient for those projects for which the uncertainty about the development is low. There is, however, an increasing number of new prototypical compounds resulting from the increased biological knowledge with a high level of uncertainty. For these prototypical drugs development has to proceed in a much more adaptive manner, using tailor-made objectives, the development of special methodology and a cyclical rather than a linear type of project management.

This is a preview of subscription content, access via your institution

Access options

Buy this article

Prices may be subject to local taxes which are calculated during checkout

Figure 1: The account of the foxglove and its medical uses.
Figure 2: Determining the prototypical nature of a project.
Figure 3: Linear non-translational development.
Figure 4: Representation of ascending dose study design.
Figure 5: Translational drug development.
Figure 6: A first-in-human pharmacology experiment.
Figure 7: A schematic to determine the objectives using the question-based approach.

Similar content being viewed by others

References

  1. William Withering. An Account of the Foxglove and its Medical Uses (Oxford Univ. Press, London, 1785).

  2. Ng, R. Drugs. From discovery to approval 2nd edn (John Wiley & Sons, Hoboken, New Jersey, 2009).

    Google ScholarĀ 

  3. Rang, H. P. Drug Discovery and Development. 1st edn (Churchill Livingstone, Elsevier, Philadelphia, 2007).

    Google ScholarĀ 

  4. Cross, J. et al. Postmarketing drug dosage changes of 499 FDA-approved new molecular entities, 1980ā€“1999. Pharmacoepidemiol. Drug Saf. 11, 439ā€“446 (2002).

    ArticleĀ  Google ScholarĀ 

  5. Bhogal, N. & Combes, R. TGN1412: time to change the paradigm for the testing of new pharmaceuticals. Altern. Lab. Anim. 34, 225ā€“239 (2006).

    CASĀ  PubMedĀ  Google ScholarĀ 

  6. Clark, R. W. et al. Raising high-density lipoprotein in humans through inhibition of cholesteryl ester transfer protein: an initial multidose study of torcetrapib. Arterioscler. Thromb. Vasc. Biol. 24, 490ā€“497 (2004).

    ArticleĀ  CASĀ  Google ScholarĀ 

  7. Zhao, L., Jin, W., Rader, D., Packard, C. & Feuerstein, G. A translational medicine perspective of the development of torcetrapib: does the failure of torcetrapib development cast a shadow on future development of lipid modifying agents, HDL elevation strategies or CETP as a viable molecular target for atherosclerosis? A case study of the use of biomarkers and translational medicine in atherosclerosis drug discovery and development. Biochem. Pharmacol. 78, 315ā€“325 (2009).

    ArticleĀ  CASĀ  Google ScholarĀ 

  8. US Food and Drug Administration. Note for guidance on general considerations for clinical trials. Fed. Regist. 62(242), 66113ā€“66119 (1997).

  9. Lenfle, S. & Loch, C. Lost roots. How project management settled on the phased approach (and compromised its ability to lead change in modern enterprises). Ecole Polytechnique website [online], (2009).

    Google ScholarĀ 

  10. Loch, C., DeMeyer, A. & Pich, M. Managing the unknown. A new approach to managing high uncertainty and risk in projects. (John Wiley & Sons, Hoboken, New Jersey, 2006).

    BookĀ  Google ScholarĀ 

  11. Shuchman, M. Commercializing clinical trials-risks and benefits of the CRO boom. N. Engl. J. Med. 357, 1365ā€“1368 (2007).

    ArticleĀ  CASĀ  Google ScholarĀ 

  12. Bresalier, R. S. et al. Cardiovascular events associated with rofecoxib in a colorectal adenoma chemoprevention trial. N. Engl. J. Med. 352, 1092ā€“1102 (2005).

    ArticleĀ  CASĀ  Google ScholarĀ 

  13. Garnier, J. P. Rebuilding the R&D engine in big pharma. Harv. Bus Rev. 86, 68ā€“70, 72ā€“76, 128 (2008).

    PubMedĀ  Google ScholarĀ 

  14. Cuatrecasas, P. Drug discovery in jeopardy. J. Clin. Invest. 116, 2837ā€“2842 (2006).

    ArticleĀ  CASĀ  Google ScholarĀ 

  15. Munos, B. Lessons from 60 years of pharmaceutical innovation. Nature Rev. Drug Discov. 8, 959ā€“968 (2009).

    ArticleĀ  CASĀ  Google ScholarĀ 

  16. Lehman Brothers. The fruits of genomics. Drug pipelines face indigestion until the new biology ripens. (Lehman Brothers, New York, 2001).

  17. US Food and Drug Administration. Challenge and opportunity on the critical path to new medical products. FDA website [online], (2004).

  18. Loch, C., Mihm, J. & Huchzermeier, A. Concurrent engineering and design oscillations in complex engineering projects. Concurrent Eng. 11, 187ā€“199 (2003).

    ArticleĀ  Google ScholarĀ 

  19. Allen, T., Thusman, M. & Lee, D. Technology transfer as a function of position in the spectrum from research through development to technical services. Acad. Manage. J. 22, 694ā€“708 (1979).

    Google ScholarĀ 

  20. Roussel P. A., Saad, K. N. & Erickson, T. J. Third generation R&D: Managing the Link to Corporate Strategy 1st edn (Harvard Bus School Press, Boston, Massachusetts, USA, 1991).

    Google ScholarĀ 

  21. Sheiner, L. B. Learning versus confirming in clinical drug development. Clin. Pharmacol. Ther. 61, 275ā€“291 (1997).

    ArticleĀ  CASĀ  Google ScholarĀ 

  22. Danhof, M., Alvan, G., Dahl, S. G., Kuhlmann, J. & Paintaud, G. Mechanism-based pharmacokineticā€“pharmacodynamic modeling-a new classification of biomarkers. Pharm. Res. 22, 1432ā€“1437 (2005).

    ArticleĀ  CASĀ  Google ScholarĀ 

  23. FDA Center for Drug Evaluation and Research. Exploratory I.N.D. Studies. FDA website [online], (2006).

  24. Kenter, M. J. & Cohen, A. F. Establishing risk of human experimentation with drugs: lessons from TGN1412. Lancet 368, 1387ā€“1391 (2006).

    ArticleĀ  CASĀ  Google ScholarĀ 

  25. Cohen, A. Pharmacokinetic and pharmacodynamic data to be derived from early-phase drug development: designing informative human pharmacology studies. Clin. Pharmacokinet. 47, 373ā€“381 (2008).

    ArticleĀ  CASĀ  Google ScholarĀ 

  26. FDA Center for Drug Evaluation and Research. Estimating the maximum safe starting dose in initial clinical trials for therapeutics in adult healthy volunteers. Guidance for Industry. FDA website [online], (2005).

  27. Cohen, A. Should we tolerate tolerability as an objective in early drug development? Br. J. Clin. Pharmacol. 64, 249ā€“252 (2007).

    ArticleĀ  CASĀ  Google ScholarĀ 

  28. Schein, P. S. et al. The evaluation of anticancer drugs in dogs and monkeys for the prediction of qualitative toxicities in man. Clin. Pharmacol. Ther. 11, 3ā€“40 (1970).

    ArticleĀ  CASĀ  Google ScholarĀ 

  29. Freireich, E. J., Gehan, E. A., Rall, D. P., Schmidt, L. H. & Skipper, H. E. Quantitative comparison of toxicity of anticancer agents in mouse, rat, hamster, dog, monkey and man. Cancer Chemother. Rep. 50, 219ā€“244 (1966).

    CASĀ  PubMedĀ  Google ScholarĀ 

  30. Zhou, H. et al. Effect of meal timing not critical for the pharmacokinetics of tegaserod (HTF 919). J. Clin. Pharmacol. 39, 911ā€“919 (1999).

    ArticleĀ  CASĀ  Google ScholarĀ 

  31. Appel, S., Kumle, A., Hubert, M. & Duvauchelle, T. First pharmacokineticā€“pharmacodynamic study in humans with a selective 5-hydroxytryptamine4 receptor agonist. J. Clin. Pharmacol. 37, 229ā€“237 (1997).

    ArticleĀ  CASĀ  Google ScholarĀ 

  32. Chan K. Y. et al. Functional characterization of contractions to tegaserod in human isolated proximal and distal coronary arteries. Eur. J. Pharmacol. 619, 61ā€“67 (2009).

    ArticleĀ  CASĀ  Google ScholarĀ 

  33. Farzaneh, L., Kasahara, N. & Farzaneh, F. The strange case of TGN1412. Cancer Immunol. Immunother. 56, 129ā€“134 (2007).

    ArticleĀ  CASĀ  Google ScholarĀ 

  34. Legrand, N. et al. Transient accumulation of human mature thymocytes and regulatory T cells with CD28 superagonist in ā€œhuman immune systemā€ Rag2(āˆ’/āˆ’)Ī³c(āˆ’/āˆ’) mice. Blood 108, 238ā€“245 (2006).

    ArticleĀ  CASĀ  Google ScholarĀ 

  35. Expert Scientific Group on Phase One clinical Trials. Final Report (The Stationary Office, Norwich, UK, 2006).

  36. de Visser, S. J. et al. Concentration-effect relationships of two rilmenidine single-dose infusion rates in hypertensive patients. Clin. Pharmacol. Ther. 72, 419ā€“428 (2002).

    ArticleĀ  CASĀ  Google ScholarĀ 

  37. van der Post, J. P., de Visser, S. J., Schoemaker, R. C., Cohen, A. F. & van Gerven, J. M. Pharmacokinetic/pharmacodynamic assessment of tolerance to central nervous system effects of a 3Ā mg sustained release tablet of rilmenidine in hypertensive patients. J. Psychopharmacol. 18, 221ā€“227 (2004).

    ArticleĀ  CASĀ  Google ScholarĀ 

  38. de Visser, S. J. et al. Biomarkers for the effects of benzodiazepines in healthy volunteers. Br. J. Clin. Pharmacol. 55, 39ā€“50 (2003).

    ArticleĀ  CASĀ  Google ScholarĀ 

  39. Brisbare-Roch, C. et al. Promotion of sleep by targeting the orexin system in rats, dogs and humans. Nature Med. 13, 150ā€“155 (2007).

    ArticleĀ  CASĀ  Google ScholarĀ 

  40. de Visser, S. J. A question based approach to drug development. Thesis, Leiden Univ. (2003).

    Google ScholarĀ 

  41. Aronson, J. K. & Ferner, R. E. Joining the DoTS: new approach to classifying adverse drug reactions. BMJ 327, 1222ā€“1225 (2003).

    ArticleĀ  CASĀ  Google ScholarĀ 

  42. Franson, K. L. & Cohen, A. F. How it works. Br. J. Clin. Pharmacol. 68, 315ā€“317 (2009).

    ArticleĀ  CASĀ  Google ScholarĀ 

  43. Brunton, L., Blumenthal, D., Buxton, I. & Parker, K. Goodman and Gilman's Manual of Pharmacology and Therapeutics (McGraw Hill Medical, USA, 2006).

    Google ScholarĀ 

  44. Dollery, C. T. Clinical pharmacology in the molecular era. Clin. Pharmacol. Ther. 83, 220ā€“225 (2008).

    ArticleĀ  CASĀ  Google ScholarĀ 

  45. Aronson, J. An account of the foxglove and its medical uses, 1785ā€“1985. (Oxford Univ. Pres, London 1985). Clin. Pharmacol. Ther. 83, 220ā€“225 (2008).

    Google ScholarĀ 

  46. van Gerven, J. M. et al. Integrated pharmacokinetics and pharmacodynamics of Ro 48ā€“8684, a new benzodiazepine, in comparison with midazolam during first administration to healthy male subjects. Br. J. Clin. Pharmacol. 44, 487ā€“493 (1997).

    ArticleĀ  CASĀ  Google ScholarĀ 

Download references

Acknowledgements

I am indebted to my close colleagues at the Centre for Human Drug Research, Leiden, The Netherlands, particularly J. van Gerven and K. Burggraaf, for their input in the ideas that form the basis for this article. M. Kenter, D. Breimer and P. van Brummelen provided constructive criticism and suggestions.

Author information

Authors and Affiliations

Authors

Ethics declarations

Competing interests

The author declares no competing financial interests.

Related links

Related links

FURTHER INFORMATION

AstraZeneca's Annual Report 2006

Central Committee on Research Involving Human Subjects

Note for Guidance on Repeated Toxicity (CPMP/SWP/1042/99)

Author's homepage

Rights and permissions

Reprints and permissions

About this article

Cite this article

Cohen, A. Developing drug prototypes: pharmacology replaces safety and tolerability?. Nat Rev Drug Discov 9, 856ā€“865 (2010). https://doi.org/10.1038/nrd3227

Download citation

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1038/nrd3227

This article is cited by

Search

Quick links

Nature Briefing: Translational Research

Sign up for the Nature Briefing: Translational Research newsletter ā€” top stories in biotechnology, drug discovery and pharma.

Get what matters in translational research, free to your inbox weekly. Sign up for Nature Briefing: Translational Research