2017
DOI: 10.15406/japlr.2017.05.00136
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Antimalaria Drug Development & Pipeline

Abstract: Increasing incidence of artemisin resistance endangers very foundations of current guideline based antimalarial therapy. There is an unmet need to develop newer strategies, targeting novel pathophysiology to set high standards in antimalaria care. Of late, the antimalarial drug pipeline is becoming increasingly robust, and promises healthier outcomes. We discuss few drugs currently under pre-clinical development that have shown encouraging results.

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Cited by 5 publications
(6 citation statements)
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“…7). 111 Biosurfactants possess certain interesting physicochemical properties by which they can maintain their integrity while being delivered as an aerosol. This mode of delivery endows biosurfactants with a drug carrier-like feature considering the lungs as the main area of action.…”
Section: Biosurfactantsmentioning
confidence: 99%
See 1 more Smart Citation
“…7). 111 Biosurfactants possess certain interesting physicochemical properties by which they can maintain their integrity while being delivered as an aerosol. This mode of delivery endows biosurfactants with a drug carrier-like feature considering the lungs as the main area of action.…”
Section: Biosurfactantsmentioning
confidence: 99%
“…The amphiphilic structure of biosurfactant suggests, that the water-fearing layer can react with the lipid layer of the virus, as concomitantly reacting with hydrophobic substances like H 2 O. This unique amphiphilic nature is the cornerstone of biosurfactant structure which is very beneficial to disrupt virus structure 111.…”
mentioning
confidence: 99%
“…[ 176 ] A simpler metabolism, low toxicity, and amodiaquine‐like activity were shown by GSK369796; however, the compound was not found to be as effective as chloroquine. [ 177,178 ]…”
Section: Malariamentioning
confidence: 99%
“…[176] A simpler metabolism, low toxicity, and amodiaquine-like activity were shown by GSK369796; however, the compound was not found to be as effective as chloroquine. [177,178] ACT-451840 (53) was discovered in a phenotypic screening and showed dual activity against asexual and sexual stages of P. falciparum and P. vivax, showing good gametocidal activity, fast action, and longer half-life than artemisinin. [179,180] The exposure of 53 is increased fourteen times in the presence of fatty and caloric foods.…”
Section: Antimalarial Candidates In Phase IIImentioning
confidence: 99%
“…SC83288 (an amicarbalide derivative) is the only agent in preclinical investigation that are going to treat sever malaria [208]. It is also possible to list Genz-668764, ML238, ACT-213615, and TDR84420 within the new chemical entity group [209].…”
Section: Drugs In the Pipelinementioning
confidence: 99%