Literature DB >> 16579068

Development of new drugs for chemoprophylaxis of malaria.

W Milhous1.   

Abstract

When U.S. troops first encountered drug resistant malaria during the Vietnam war, the United States Army responded by establishing a malaria drug research program. In 1988, the Walter Reed Army Institute of Research developed mefloquine (WR 149240) and halofantrine (WR 171669). Actually in association with SmithKline Beecham, the WRAIR is developing tafenoquine (WR 238605), an analogue of primaquine, which is expected to be effective in both preventing and treating malaria in deployed military personnel. Final phase III studies leading to U.S. Food and Drug Administration approval are planned for 2000. Applied research is also carried out with the association atovaquone-proguanil (Malarone) or with azithromycin, but also with primaquine, the associations paludrine-dapsone or lapudrine-dapsone, analogues of floxacrine (WR 243251), and a guanylhydrazone (WR 182393). The future scientific directions must focus on basic and applied research for a better understanding of the modes of action and mechanisms of resistance to standard and developmental drugs. Using new techniques, the design and synthesis of new drugs would hopefully result in the development of drugs that circumvent the malaria parasites elusive mechanisms of drug resistance.

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Year:  2001        PMID: 16579068

Source DB:  PubMed          Journal:  Bull Soc Pathol Exot        ISSN: 0037-9085


  4 in total

Review 1.  A lesson learnt: the rise and fall of Lariam and Halfan.

Authors:  Ashley M Croft
Journal:  J R Soc Med       Date:  2007-04       Impact factor: 5.344

2.  Reinventing primaquine for endemic malaria.

Authors:  John Kevin Baird
Journal:  Expert Opin Emerg Drugs       Date:  2012-09-21       Impact factor: 4.191

3.  Walter Reed Army Institute of Research (WRAIR): Fifty Years of Achievements That Impact Science and Society.

Authors:  Carl R Alving
Journal:  Mil Med       Date:  2021-02-26       Impact factor: 1.437

4.  Comparative protein modeling of spermidine synthase from Plasmodium falciparum: A potential target for anti-malarial drug therapy.

Authors:  Duvvuru Muni Rajasekhara Reddy
Journal:  Bioinformation       Date:  2006-12-23
  4 in total

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