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FURTHER READING 461<br />

The excitement engendered by these<br />

advances must be tempered by the realities of<br />

drug development and production. The first<br />

hurdle is drug toxicity. At times predictable,<br />

but often idiosyncratic, unexpected untoward<br />

effects have prevented the use of many otherwise<br />

effective anti-parasitic drugs. Particularly<br />

troublesome are serious toxicities that occur<br />

at low frequency. They may come to attention<br />

only after a drug has been marketed.<br />

To be successful, new drugs must also have<br />

favorable pharmacodynamics. Oral administration<br />

in a single dose or several doses on one<br />

day is particularly important for mass treatment<br />

programs in areas where the lack of education,<br />

refrigeration and other logistic factors<br />

may interfere with compliance.<br />

The economic realities of new drug development<br />

must also be considered. Many parasitic<br />

diseases are endemic in impoverished<br />

areas where the likelihood of profits is too<br />

small to engender investment by major pharmaceutical<br />

companies. Even if a highly effective<br />

anti-parasitic drug is identified, the cost of<br />

development may be prohibitive.<br />

The cost of production is also critical as<br />

illustrated by eflornithine. It seems tragic that<br />

the manufacture of an effective anti-parasitic<br />

drugs should cease for economic reasons at a<br />

time when the drug is critically needed. The<br />

story can be different for drugs that are used in<br />

industrialized countries for other human indications<br />

or veterinary infections. As illustrated<br />

by ivermectin, which is marketed for the treatment<br />

of the dog heartworm, Dirofilaria immitis,<br />

veterinary use and profits have offset production<br />

costs. Ivermectin has been donated<br />

by the manufacturer for the treatment of<br />

onchocerciasis.<br />

There are no simple answers to the economic<br />

constraints on basic research, drug development<br />

and production. There is increasing realization<br />

that health is an issue of international<br />

security. The World Health Organization, World<br />

Bank, National Institutes of Health, Gates<br />

Foundation and other governmental and<br />

non-governmental groups have increasingly<br />

focused their resources on diseases of the nonindustrialized<br />

world. Their continued support is<br />

critical to the development, production and<br />

distribution of new anti-parasitic drugs. The<br />

future seems bright, but it will take a concerted<br />

effort to bring the fruits of modern science to<br />

the bedside of the poor who suffer from parasitic<br />

diseases.<br />

FURTHER READING<br />

Anon. (2002). Drugs for parasitic infections. Med.<br />

Lett. Drugs Ther. 1–12, [online].<br />

Campbell, W.C., Fisher, M.H., Stapley, E.O. et al.<br />

(1983) Ivermectin: a potent new antiparasitic<br />

agent. Science 221, 823–828.<br />

Gillespie, S.I. and Pearson, R.D. (eds) (2001).<br />

Principles and Practice of Clinical Parasitology,<br />

Chichester: John Wiley and Sons.<br />

Guerrant, R.L., Walker, D.H. and Weller, P.F. (eds)<br />

(1999). Tropical Infectious Diseases: Principles,<br />

Pathogens and Practice. New York: Churchill<br />

Livingstone.<br />

Guttman, P. and Ehrlich, P. (1891). Ueber die wirkung<br />

des methyleneblau bei malaria. Berlin Klin.<br />

Wochenschr. 28, 953–956.<br />

Hardman, J.G. and Limbird, L.E. (eds) (2001).<br />

Goodman and Gilman’s Pharmacological Basis<br />

of Therapeutics, New York: McGraw-Hill.<br />

Health Information for International Travel,<br />

2001–2002. Atlanta, GA: US Department of Health<br />

and Human Services, Public Health Service,<br />

Centers for Disease Control and Prevention.<br />

Horton, J. (2000). Albendazole: a review of<br />

anthelmintic efficacy and safety in humans.<br />

Parasitology 121, Suppl., S113–S132.<br />

Jha, T.K., Sundar, S., Thakur, C.P. et al. (1999)<br />

Miltefosine, an oral agent, for the treatment of<br />

Indian visceral leishmaniasis. N. Engl. J. Med.<br />

341, 1795–1800.<br />

King, C.H. and Mahmoud, A.A. (1989). Drugs five<br />

years later: praziquantel. Ann. Intern. Med. 110,<br />

290–296.<br />

MEDICAL APPLICATIONS

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