Evidence map›Paper›PMID 29802605›Full record

ReviewDrugs2018

Drugs in Development for Malaria.

Elizabeth A Ashley, Aung Pyae Phyo

Open access · hybridAbstract readReview
In one paragraph

Review in Drugs, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 82 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
82citing papers in PubMed, 1 pooled it
23.7field-weighted citation impact, top 1% of its field
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

82 citing papers in PubMed, 1 synthesis or guideline pooled it, 218 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. Review
  5. Article
  6. Article
  7. Application of a Non-Targeted Metabolomics Study inInternational journal of molecular sciences · 2025
    Article
  8. Article
  9. Article
  10. Review
  11. Article
  12. Controlling Malaria on the Road to Elimination: A View from 10 Years Later.The American journal of tropical medicine and hygiene · 2025
    Article
  13. Review
  14. Article
  15. Review
  16. Article
  17. Malaria during COVID-19 Travel Restrictions in Makkah, Saudi Arabia.Tropical medicine and infectious disease · 2024
    Article
  18. Article
  19. Review
  20. Review

22 more citing papers are in PubMed but not listed here.

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

2 authors at 2 institutions in 3 countries.

Elizabeth A AshleyMyanmar Oxford Clinical Research Unit, Yangon, Myanmar. liz@tropmedres.ac.ORCID http://orcid.org/0000-0002-7620-4822
Aung Pyae PhyoMyanmar Oxford Clinical Research Unit, Yangon, Myanmar.
Angkor Hospital for Children · KHMyanmar Oxford Clinical Research Unit · MM

Funding

Wellcome Trust
6 · The paper itself

Abstract

The last two decades have seen a surge in antimalarial drug development with product development partnerships taking a leading role. Resistance of Plasmodium falciparum to the artemisinin derivatives, piperaquine and mefloquine in Southeast Asia means new antimalarials are needed with some urgency. There are at least 13 agents in clinical development. Most of these are blood schizonticides for the treatment of uncomplicated falciparum malaria, under evaluation either singly or as part of two-drug combinations. Leading candidates progressing through the pipeline are artefenomel-ferroquine and lumefantrine-KAF156, both in Phase 2b. Treatment of severe malaria continues to rely on two parenteral drugs with ancient forebears: artesunate and quinine, with sevuparin being evaluated as an adjuvant therapy. Tafenoquine is under review by stringent regulatory authorities for approval as a single-dose treatment for Plasmodium vivax relapse prevention. This represents an advance over standard 14-day primaquine regimens; however, the risk of acute haemolytic anaemia in patients with glucose-6-phosphate dehydrogenase deficiency remains. For disease prevention, several of the newer agents show potential but are unlikely to be recommended for use in the main target groups of pregnant women and young children for some years. Latest predictions are that the malaria burden will continue to be high in the coming decades. This fact, coupled with the repeated loss of antimalarials to resistance, indicates that new antimalarials will be needed for years to come. Failure of the artemisinin-based combinations in Southeast Asia has stimulated a reappraisal of current approaches to combination therapy for malaria with incorporation of three or more drugs in a single treatment under consideration.

Indexed as

AminoquinolinesAntimalarialsArtemisininsDrug DiscoveryDrug Resistance, MultipleFerrous CompoundsHumansImidazolesLumefantrineMalariaMetallocenesPiperazinesSignal TransductionTreatment OutcomeAminoquinolinesAntimalarialsartemisininArtemisininsferroquineFerrous CompoundsganaplacideImidazolesLumefantrineMetallocenesPiperazinestafenoquine

Identifiers

PMID29802605
PMCPMC6013505
OpenAlexW2803912078

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.