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Scoping Review of Antimalarial Drug Candidates in Phase I and II Drug Development

The emergence and spread of parasite resistance to currently available antimalarials has highlighted the importance of developing novel antimalarials. This scoping review provides an overview of antimalarial drug candidates undergoing phase I and II studies between 1 January 2016 and 28 April 2021....

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Autores principales: Abd-Rahman, Azrin N., Zaloumis, Sophie, McCarthy, James S., Simpson, Julie A., Commons, Robert J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society for Microbiology 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8846400/
https://www.ncbi.nlm.nih.gov/pubmed/34843390
http://dx.doi.org/10.1128/aac.01659-21
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author Abd-Rahman, Azrin N.
Zaloumis, Sophie
McCarthy, James S.
Simpson, Julie A.
Commons, Robert J.
author_facet Abd-Rahman, Azrin N.
Zaloumis, Sophie
McCarthy, James S.
Simpson, Julie A.
Commons, Robert J.
author_sort Abd-Rahman, Azrin N.
collection PubMed
description The emergence and spread of parasite resistance to currently available antimalarials has highlighted the importance of developing novel antimalarials. This scoping review provides an overview of antimalarial drug candidates undergoing phase I and II studies between 1 January 2016 and 28 April 2021. PubMed, Web of Science, Embase, clinical trial registries, and reference lists were searched for relevant studies. Information regarding antimalarial compound details, clinical trial characteristics, study population, and drug pharmacokinetics and pharmacodynamics (PK-PD) were extracted. A total of 50 studies were included, of which 24 had published their results and 26 were unpublished. New antimalarial compounds were evaluated as monotherapy (28 studies, 14 drug candidates) and combination therapy (9 studies, 10 candidates). Fourteen active compounds were identified in the current antimalarial drug development pipeline together with 11 compounds that are inactive, 6 due to insufficient efficacy. PK-PD data were available from 24 studies published as open-access articles. Four unpublished studies have made their results publicly available on clinical trial registries. The terminal elimination half-life of new antimalarial compounds ranged from 14.7 to 483 h. The log(10) parasite reduction ratio over 48 h and parasite clearance half-life for Plasmodium falciparum following a single-dose monotherapy were 1.55 to 4.1 and 3.4 to 9.4 h, respectively. The antimalarial drug development landscape has seen a number of novel compounds, with promising PK-PD properties, evaluated in phase I and II studies over the past 5 years. Timely public disclosure of PK-PD data is crucial for informative decision-making and drug development strategy.
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spelling pubmed-88464002022-03-03 Scoping Review of Antimalarial Drug Candidates in Phase I and II Drug Development Abd-Rahman, Azrin N. Zaloumis, Sophie McCarthy, James S. Simpson, Julie A. Commons, Robert J. Antimicrob Agents Chemother Minireview The emergence and spread of parasite resistance to currently available antimalarials has highlighted the importance of developing novel antimalarials. This scoping review provides an overview of antimalarial drug candidates undergoing phase I and II studies between 1 January 2016 and 28 April 2021. PubMed, Web of Science, Embase, clinical trial registries, and reference lists were searched for relevant studies. Information regarding antimalarial compound details, clinical trial characteristics, study population, and drug pharmacokinetics and pharmacodynamics (PK-PD) were extracted. A total of 50 studies were included, of which 24 had published their results and 26 were unpublished. New antimalarial compounds were evaluated as monotherapy (28 studies, 14 drug candidates) and combination therapy (9 studies, 10 candidates). Fourteen active compounds were identified in the current antimalarial drug development pipeline together with 11 compounds that are inactive, 6 due to insufficient efficacy. PK-PD data were available from 24 studies published as open-access articles. Four unpublished studies have made their results publicly available on clinical trial registries. The terminal elimination half-life of new antimalarial compounds ranged from 14.7 to 483 h. The log(10) parasite reduction ratio over 48 h and parasite clearance half-life for Plasmodium falciparum following a single-dose monotherapy were 1.55 to 4.1 and 3.4 to 9.4 h, respectively. The antimalarial drug development landscape has seen a number of novel compounds, with promising PK-PD properties, evaluated in phase I and II studies over the past 5 years. Timely public disclosure of PK-PD data is crucial for informative decision-making and drug development strategy. American Society for Microbiology 2022-02-15 /pmc/articles/PMC8846400/ /pubmed/34843390 http://dx.doi.org/10.1128/aac.01659-21 Text en Copyright © 2022 Abd-Rahman et al. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International license (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Minireview
Abd-Rahman, Azrin N.
Zaloumis, Sophie
McCarthy, James S.
Simpson, Julie A.
Commons, Robert J.
Scoping Review of Antimalarial Drug Candidates in Phase I and II Drug Development
title Scoping Review of Antimalarial Drug Candidates in Phase I and II Drug Development
title_full Scoping Review of Antimalarial Drug Candidates in Phase I and II Drug Development
title_fullStr Scoping Review of Antimalarial Drug Candidates in Phase I and II Drug Development
title_full_unstemmed Scoping Review of Antimalarial Drug Candidates in Phase I and II Drug Development
title_short Scoping Review of Antimalarial Drug Candidates in Phase I and II Drug Development
title_sort scoping review of antimalarial drug candidates in phase i and ii drug development
topic Minireview
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8846400/
https://www.ncbi.nlm.nih.gov/pubmed/34843390
http://dx.doi.org/10.1128/aac.01659-21
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