Evidence map›Paper›PMID 22877082›Full record

ArticleMalaria journal2012

Review of pyronaridine anti-malarial properties and product characteristics.

Simon L Croft, Stephan Duparc, Sarah J Arbe-Barnes, J Carl Craft, Chang-Sik Shin, Lawrence Fleckenstein, Isabelle Borghini-Fuhrer, Han-Jong Rim

Registry-linked trialOpen access · goldAbstract read
In one paragraph

Article in Malaria journal, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT04783051 (Comparison of IST Using Ultra-sensitive Malaria Rapid Diagnostic Test and Pyronaridine - Artesunate - PYRAMAX®) to Standard IPT Sulfadoxine-pyrimethamine to Prevent Malaria in Pregnant Women Living in Endemic Areas), which is not on this map. Cited by 84 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
84citing papers in PubMed, 3 pooled it
9.1field-weighted citation impact, top 2% 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.

NCT04783051 phase3completednot on this mapstarted 2021, after this paper: background citation

Comparison of IST Using Ultra-sensitive Malaria Rapid Diagnostic Test and Pyronaridine - Artesunate - PYRAMAX®) to Standard IPT Sulfadoxine-pyrimethamine to Prevent Malaria in Pregnant Women Living in Endemic Areas

TypeinterventionalSponsorUniversity of KinshasaRan2021 to 2022Enrolled250ConditionsMalaria in PregnancyArmsSulfadoxine pyrimethamine, Pyramax
3 · Its place in the literature

Who cites it

84 citing papers in PubMed, 3 syntheses or guidelines pooled it, 155 citations in OpenAlex.

  1. Pooled it
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  8. Mass balance and metabolism of the antimalarial pyronaridine in healthy volunteers.European journal of drug metabolism and pharmacokinetics · 2015
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  11. Article
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  16. Review
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  18. Malaria: past, present, and future.Signal transduction and targeted therapy · 2025
    Review
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  20. Review

24 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

8 authors at 6 institutions in 4 countries.

Simon L CroftFaculty of Infectious and Tropical Diseases, London School of Hygiene and Tropical Medicine, Keppel Street, London, WC1E 7HT, UK. simon.croft@lshtm.ac.uk
Stephan Duparc
Sarah J Arbe-Barnes
J Carl Craft
Chang-Sik Shin
Lawrence Fleckenstein
Isabelle Borghini-Fuhrer
Han-Jong Rim
Medicines for Malaria Venture · CHKorea University · KRLondon School of Hygiene & Tropical Medicine · GBShin Poong Pharm (South Korea) · KRStevenage Bioscience Catalyst · GBUniversity of Iowa · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Pyronaridine was synthesized in 1970 at the Institute of Chinese Parasitic Disease and has been used in China for over 30 years for the treatment of malaria. Pyronaridine has high potency against Plasmodium falciparum, including chloroquine-resistant strains. Studies in various animal models have shown pyronaridine to be effective against strains resistant to other anti-malarials, including chloroquine. Resistance to pyronaridine appears to emerge slowly and is further retarded when pyronaridine is used in combination with other anti-malarials, in particular, artesunate. Pyronaridine toxicity is generally less than that of chloroquine, though evidence of embryotoxicity in rodents suggests use with caution in pregnancy. Clinical pharmacokinetic data for pyronaridine indicates an elimination T1/2 of 13.2 and 9.6 days, respectively, in adults and children with acute uncomplicated falciparum and vivax malaria in artemisinin-combination therapy. Clinical data for mono or combined pyronaridine therapy show excellent anti-malarial effects against P. falciparum and studies of combination therapy also show promise against Plasmodium vivax. Pyronaridine has been developed as a fixed dose combination therapy, in a 3:1 ratio, with artesunate for the treatment of acute uncomplicated P. falciparum malaria and blood stage P. vivax malaria with the name of Pyramax® and has received Positive Opinion by European Medicines Agency under the Article 58 procedure.

Indexed as

AntimalarialsChinaDrug-Related Side Effects and Adverse ReactionsDrug Therapy, CombinationHumansMalaria, FalciparumMalaria, VivaxNaphthyridinesPlasmodium falciparumPlasmodium vivaxTreatment OutcomeAntimalarialsNaphthyridinespyronaridine

Identifiers

PMID22877082
PMCPMC3483207
OpenAlexW2139242164

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

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.