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24 - Developing the next generation of botulinum toxin drugs

Published online by Cambridge University Press:  28 July 2009

Daniel Truong
Affiliation:
Orange Coast Memorial Medical Center
Dirk Dressler
Affiliation:
Hannover Medical School, Hannover, Germany
Mark Hallett
Affiliation:
George Washington University School of Medicine and Health Sciences, Washington, DC
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Summary

Botulinum toxin (BoNT) has now been used for more than 20 years with remarkable success to treat various conditions caused by hyperactivity of muscles or exocrine glands (Scott, 1980; Moore & Naumann, 2003). Its use for treatment of pain syndromes is currently being explored. For most of its indications BoNT therapy is the therapy of choice. For some it has revolutionized therapy altogether. This, together with its exploding use in cosmetics, has generated an industry with annual sales in excess of one billion US dollars. However, 20 years into this therapy, we are still using more or less the original BoNT drugs.

As shown in Figure 24.1 the first BoNT drug was registered in 1989 as Oculinum®. In 1992 its name was changed to Botox®. In 1999 a modified formulation of Botox was marketed without a name change. In 1991 Dysport® was registered as another BoNT type A drug and in 2000 NeuroBloc®/Myobloc® became available as the first – and so far only – BoNT type B drug. When NeuroBloc/Myobloc was introduced to the neurological community it soon became apparent that it has a much stronger affinity to autonomic synapses than to motor synapses as compared to BoNT type A drugs (Dressler & Benecke, 2003) thus producing frequent autonomic side effects in the treatment of motor disorders. This, together with its high antigenicity (Dressler & Bigalke, 2004), has prevented its large-scale use. In 2005 Xeomin® was marketed in Germany.

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Publisher: Cambridge University Press
Print publication year: 2009

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References

Dressler, D. & Benecke, R. (2003). Autonomic side effects of botulinum toxin type B treatment of cervical dystonia and hyperhidrosis. Eur Neurol, 49, 34–8.CrossRefGoogle ScholarPubMed
Dressler, D. & Bigalke, H. (2004). Antibody-induced failure of botulinum toxin type B therapy in de novo patients. Eur Neurol, 52, 132–5.CrossRefGoogle ScholarPubMed
Dressler, D. & Dirnberger, G. (2000). Botulinum toxin therapy: risk factors for therapy failure. Mov Disord, 15(Suppl 2), 51.Google Scholar
Dressler, D. & Hallett, M. (2006). Immunological aspects of Botox, Dysport, and Myobloc/NeuroBloc. Eur J Neurol, 13(Suppl 1), 11–15.CrossRefGoogle ScholarPubMed
Hott, J. S., Dalakas, M. C., Sung, C., Hallett, M. & Youle, R. J. (1998). Skeletal muscle-specific immunotoxin for the treatment of focal muscle spasm. Neurology, 50, 485–91.CrossRefGoogle ScholarPubMed
Jankovic, J., Vuong, K. D. & Ahsan, J. (2003). Comparison of efficacy and immunogenicity of original versus current botulinum toxin in cervical dystonia. Neurology, 60, 1186–8.CrossRefGoogle ScholarPubMed
Lee, J. C., Yokota, K., Arimitsu, H., et al. (2005). Production of anti-neurotoxin antibody is enhanced by two subcomponents, HA1 and HA3b, of Clostridium botulinum type B 16S toxin-haemagglutinin. Microbiology, 151, 3739–47.CrossRefGoogle ScholarPubMed
Ludlow, C. L., Hallett, M., Rhew, K., et al. (1992). Therapeutic use of type F botulinum toxin. N Engl J Med, 326, 349–50.Google ScholarPubMed
Moore, P. & Naumann, M. (2003). Handbook of Botulinum Toxin Treatment, 2nd edn. Malden, MA, USA: Blackwell Science.Google Scholar
Scott, A. B. (1980). Botulinum toxin injection into extraocular muscles as an alternative to strabismus surgery. J Pediatr Ophthalmol Strabismus, 17, 21–5.Google ScholarPubMed
Wirtschafter, J. D. & McLoon, L. K. (1998). Long-term efficacy of local doxorubicin chemomyectomy in patients with blepharospasm and hemifacial spasm. Ophthalmology, 105, 342–6.CrossRefGoogle ScholarPubMed

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