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Table 3 Limitations and desired product profiles of drugs for 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 profiles of new products

Leishmaniasis

Antimonials (1950)

Safety, poor compliance, resistance

Active against resistant strains; oral drug or safe injectable; cure in less than 28 days; pediatric formulation; potential combination with other agents; use in pregnancy; stable under tropical conditions; affordable

Pentamidine (Lomidine) (1939)

Safety, poor compliance, resistance

Amphotericin B (Fungizone) (1959)

Safety, poor compliance, resistance

Liposomal amphotericin B (AmBisome) (1990)

Safety, poor compliance, resistance

Miltefosine (2002)

Safety, poor compliance, resistance

Sodium Stibogluconate/paromomycin (SSG&PM) (2010)

Contra-indicated in pregnancy

Human African Trypanosomiasis

Suramin (1920)

Efficacy, injectable

Use against early and late stage disease; active against both major species; parenteral with option for oral use; cure in less than 14 days; pediatric formulation; potential combination with other agents; use in pregnancy; stable under tropical conditions; affordable

Melarsoprol (1949)

Safety, injectable

Pentamidine (1939)

Resistance, compliance, injectable

Eflornithine (1991)

Cost, injectable, efficacy

NECT (Nifurtimox/eflornithine) (2009)

Cost, injectable, compliance

Chagas disease

Benznidazole (1970)

Activity limited to acute stage of disease, some safety issues

Active against blood and tissue forms of parasite; active in prevention of chronic stage of the disease; pediatric formulation; potential combination with other agents; use in pregnancy; stable under tropical conditions; affordable

Nifurtimox (1974)

Activity limited to acute stage of disease, some safety issues

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