Evidence map›Paper›PMID 28992431›Full record

ReviewAnnual review of pharmacology and toxicology2018

Model-Informed Drug Development for Malaria Therapeutics.

Kayla Ann Andrews, David Wesche, James McCarthy, Jörg J Möhrle, Joel Tarning, Luann Phillips, Steven Kern, Thaddeus Grasela

Abstract readReview
In one paragraph

Review in Annual review of pharmacology and toxicology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed, 2 pooled it
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

13 citing papers in PubMed, 2 syntheses or guidelines pooled it.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors.

Kayla Ann AndrewsCognigen Corporation, a subsidiary of Simulations Plus, Buffalo, New York 14221, USA; email: Kayla.Andrews@cognigencorp.com , Luann.Phillips@cognigencorp.com , grasela@cognigencorp.com.
David WescheBill and Melinda Gates Foundation, Seattle, Washington 98109, USA; email: David.Wesche@gatesfoundation.org , Steven.Kern@gatesfoundation.org.
James McCarthyQIMR Berghofer Medical Research Institute, Brisbane, Australia.
Jörg J MöhrleMedicines for Malaria Venture, Geneva 1215, Switzerland; email: moehrlej@mmv.org.
Joel TarningMahidol-Oxford Tropical Medicine Research Unit, Faculty of Tropical Medicine, Mahidol University, Bangkok, Thailand; email: joel@tropmedres.ac.
Luann PhillipsCognigen Corporation, a subsidiary of Simulations Plus, Buffalo, New York 14221, USA; email: Kayla.Andrews@cognigencorp.com , Luann.Phillips@cognigencorp.com , grasela@cognigencorp.com.
Steven KernBill and Melinda Gates Foundation, Seattle, Washington 98109, USA; email: David.Wesche@gatesfoundation.org , Steven.Kern@gatesfoundation.org.
Thaddeus GraselaCognigen Corporation, a subsidiary of Simulations Plus, Buffalo, New York 14221, USA; email: Kayla.Andrews@cognigencorp.com , Luann.Phillips@cognigencorp.com , grasela@cognigencorp.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Malaria is a critical public health problem resulting in substantial morbidity and mortality, particularly in developing countries. Owing to the development of resistance toward current therapies, novel approaches to accelerate the development efforts of new malaria therapeutics are urgently needed. There have been significant advancements in the development of in vitro and in vivo experiments that generate data used to inform decisions about the potential merit of new compounds. A comprehensive disease-drug model capable of integrating discrete data from different preclinical and clinical components would be a valuable tool across all stages of drug development. This could have an enormous impact on the otherwise slow and resource-intensive process of traditional clinical drug development.

Indexed as

AnimalsAntimalarialsDrug DevelopmentHumansMalariaAntimalarialscontrolled human malaria infectiondisease-drug modelmalariamodel-informed drug developmentpharmacodynamicspharmacokinetics

Identifiers

PMID28992431
PMCPMC7198115

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.