An Historical Perspective of the Successful Development of Sevoflurane

Abstract

The drug development process has become extremely competitive over the past decade as regulations and patient safety concerns require lengthy and costly investigations to evaluate new products. The cost of development of a pharmaceutical product must be less than the return on investment over the market lifetime. To ensure profitability in this competitive environment, new products must penetrate global markets rapidly. Prior to entry, regulatory review and approval of a market application is required in each country.

This overview chronicles the rapid and successful drug development and global market application filing of Sevoflurane. In March 1992, Abbott Laboratories’ Hospital Products Division began to organize a clinical submission plan for Sevoflurane, a new inhalational anesthetic. To date, Sevoflurane is approved in 46 countries, including the United States. It has been well accepted in all markets. Worldwide, over 11 million patients have been exposed to Sevoflurane.

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References

  1. 1.

    Regan BM, Zimmerman SR. Anesthetic activity vs. chemical constitution of fluorinated methyl isopropyl ethers. Fed Proc. 1971;30(2):442.

    Google Scholar 

  2. 2.

    Wallin RF, Napoli MD. Sevoflurane (fluoromethyl 1,1,1,3,3,3-Hexafluoro-2-Propyl Ether): A new inhalational anesthetic agent. Fed Proc. 1971;30(2):442.

    Google Scholar 

  3. 3.

    Mapleson WW. Effect of age on MA. in humans: A meta-analysis. Br J of Anaesth. 1996;76:179–85.

    CAS  Article  Google Scholar 

  4. 4.

    Sevoflurane Package Insert. June 1995.

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Correspondence to Leticia Delgado-Herrera RPh, MS.

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The Sevoflurane Venture Team recognizes these individuals: A. Adee, A. Bartley-Arquilla, D. Belongia, S. Bohannon, C. Frosch, S. Galvez, J. Jennings, M. Klemz, Z. Latif, P. Pichotta, G. Pratt, P. Prokocimer, J. Sayre, T. Stickler, P. Vandergrift, and B. Willms; the Hospital Products Division of Abbott Laboratories: C. Begley, D. Cunningham, D. Grabenkort, J. Garapolo, S. Huang, J. Joseph, J. Kringel, J. Leedy, L. Meyer, S. Murphy, K. Pope, G. Ramsay, and M. Szela; the Pharmaceutical Products Division of Abbott Laboratories: B. Bopp, S. Burke, P. Cusick, F. Fort, M. Friedman, W. Giardina, M. Karol, K. Keller, C. Lanni, J. Machinist, D. Moyse, R. Patterson, and B. Sonders; the International Division of Abbott Laboratories: R. Bachand, D. Chapman, N. Conway, C. Fulwell, P. Guzek, M. Hodkinson, R. Horder, W. Mann, L. Mershimer, U. Ortell, J. Y. Paveé, and C. Ward; Maruishi Pharmaceuticals: K. Habuchi, K. Inoue, N. Inoue, and N. Satoh; Central Glass Company Limited: S. Inoue and Y. Kumagai; Ledell, Inc.: K. Hembrey, E. Hodosh, C. Leman, S. Rogers, and J. Wu; and outside contractors: M. Anderson, M. DeLeon, L. Garcia, V. Holem, S. Katz, J. Patrick, and N. Siddique.

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Callan, C., Delgado-Herrera, L., Guzek, D. et al. An Historical Perspective of the Successful Development of Sevoflurane. Ther Innov Regul Sci 32, 119–127 (1998). https://doi.org/10.1177/009286159803200116

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Key Words

  • Abbott Laboratories
  • Global pharmaceutical markets
  • Inhalational anesthetic
  • Pharmaceutical product development
  • Sevoflurane