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Table 2 Limitations and desired product profiles of drugs for malaria, leishmania, Human African Trypanosomiasis, and Chagas disease

From: Control of malaria and other vector-borne protozoan diseases in the tropics: enduring challenges despite considerable progress and achievements

Drugs

Limitations

Desired profile of new products

Malaria

Quinine (Quinine sulphate , Quinimax) (1930)

Compliance, resistance (1960s), safety

Active against resistant strains; oral formulations, with option for parenteral use for patients in coma; use in pediatric formulation; potential combination with other agents; use in pregnancy; cure in three days; stable under tropical conditions; inexpensive.

Chloroquine (Nivaquine , Aralen) (1945)

Resistance (1950s)

Primaquine (1948)

Safety, contra-indicated in G6PD deficiency, pregnancy

Sulphadoxine-pyrimethamine (Maloxine , Fansidar) (1961)

Resistance (1960s)

Amodiaquine (Camoquin) (1950)

Resistance, safety

Artemisinins (1994)

Cost, resistance (2008), potential neurotoxicity

Mefloquine (Lariam , Mephaquine) (1984)

Resistance (1980s), cost, contra-indicated in known or suspected history of neuropsychiatric disorder

Resistance, cost, safety, or recent (<3 weeks) use of Halofantrine

Halofantrine (1975)

Compliance, resistance potential, contra-indicated in cardiac disease and pregnancy

Artemether/lumefantrine (Coartem , Mephaquine) (2001)

Compliance, cost, resistance, GMP, potential neurotoxicity

Artesunate/amodiaquine (ASAQ) (2007)

Compliance, cost, resistance, GMP, safety, contra-indicated in pregnancy

Atovaquone/proguanil (1999)

Cost, resistance potential

Tetracycline (1940s), doxycycline (1960s)

Contra-indicated for those aged less than eight years and in pregnancy

Clindamycin (Dalacin , Lincocin) (1968)

Efficacy, contra-indicated in severe hepatic or renal impairment; history of gastrointestinal disease, especially colitis

  1. Adapted from Schiltzer [68], Nwaka and Ridley [75], Nwaka and Hudson [78] and DNDi [79].