Version 2 2021-09-16, 19:11Version 2 2021-09-16, 19:11
Version 1 2021-09-15, 14:38Version 1 2021-09-15, 14:38
journal contribution
posted on 2021-09-16, 19:11authored byBarbara Forte, Sabine Ottilie, Andrew Plater, Brice Campo, Koen J. Dechering, Francisco Javier Gamo, Daniel E. Goldberg, Eva S. Istvan, Marcus Lee, Amanda K. Lukens, Case W. McNamara, Jacquin C. Niles, John Okombo, Charisse Flerida
A. Pasaje, Miles G. Siegel, Dyann Wirth, Susan Wyllie, David A. Fidock, Beatriz Baragaña, Elizabeth A. Winzeler, Ian H. Gilbert
There is a shift
in antimalarial drug discovery from phenotypic
screening toward target-based approaches, as more potential drug targets
are being validated in Plasmodium species. Given
the high attrition rate and high cost of drug discovery, it is important
to select the targets most likely to deliver progressible drug candidates.
In this paper, we describe the criteria that we consider important
for selecting targets for antimalarial drug discovery. We describe
the analysis of a number of drug targets in the Malaria Drug Accelerator
(MalDA) pipeline, which has allowed us to prioritize targets that
are ready to enter the drug discovery process. This selection process
has also highlighted where additional data are required to inform
target progression or deprioritization of other targets. Finally,
we comment on how additional drug targets may be identified.