Evidence map›Paper›PMID 33983371›Full record

Trial reportClinical infectious diseases : an official publication of the Infectious Diseases Society of America2022

Efficacy, Safety and Tolerability of Pyronaridine-artesunate in Asymptomatic Malaria-infected Individuals: a Randomized Controlled Trial.

Edgard D Dabira, Sebastian Hachizovu, Bakary Conteh, Alieu Mendy, Haddy Nyang, Bolarinde Lawal, Mamadou Ousmane Ndiath, Joyce M Mulenga, Sydney Mwanza, Isabelle Borghini-Fuhrer and 7 more

Registry-linked trialOpen access · hybridAbstract readClinical Trial, Phase IIMulticenter StudyRandomized Controlled Trial
In one paragraph

Trial report in Clinical infectious diseases : an official publication of the Infectious Diseases Society of America, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT03814616 (A Randomized, Open-Label Exploratory Study To Determine The Efficacy Of Different Treatment Regimens Of Pyramax®), which is not on this map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.4field-weighted citation impact, top 35% 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.

NCT03814616 phase2unknown statusnot on this map

A Randomized, Open-Label Exploratory Study To Determine The Efficacy Of Different Treatment Regimens Of Pyramax® (Pyronaridine-Artesunate) In Asymptomatic Carriers Of Plasmodium Falciparum Monoinfections

TypeinterventionalSponsorShin Poong Pharmaceutical Co. Ltd.Ran2018 to 2019Enrolled300ConditionsMalaria,FalciparumArmsPyronaridine tetraphosphate 180mg:artesunate 60mg
3 · Its place in the literature

Who cites it

3 citing papers in PubMed, 6 citations in OpenAlex.

  1. Trial
  2. Review
  3. Review
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

17 authors at 4 institutions in 4 countries.

Edgard D DabiraDisease Control and Elimination Theme, Medical Research Council Unit, The Gambia at London School of Hygiene & Tropical Medicine, Fajara, The Gambia.
Sebastian HachizovuTropical Diseases Research Centre, Ndola, Zambia.
Bakary ContehDisease Control and Elimination Theme, Medical Research Council Unit, The Gambia at London School of Hygiene & Tropical Medicine, Fajara, The Gambia.
Alieu MendyDisease Control and Elimination Theme, Medical Research Council Unit, The Gambia at London School of Hygiene & Tropical Medicine, Fajara, The Gambia.
Haddy NyangDisease Control and Elimination Theme, Medical Research Council Unit, The Gambia at London School of Hygiene & Tropical Medicine, Fajara, The Gambia.
Bolarinde LawalDisease Control and Elimination Theme, Medical Research Council Unit, The Gambia at London School of Hygiene & Tropical Medicine, Fajara, The Gambia.
Mamadou Ousmane NdiathDisease Control and Elimination Theme, Medical Research Council Unit, The Gambia at London School of Hygiene & Tropical Medicine, Fajara, The Gambia.
Joyce M MulengaTropical Diseases Research Centre, Ndola, Zambia.
Sydney MwanzaTropical Diseases Research Centre, Ndola, Zambia.
Isabelle Borghini-FuhrerMedicines for Malaria Venture (MMV), Geneva, Switzerland.
Sarah Arbe-BarnesArtemida Pharma Ltd, Stevenage, United Kingdom.
Robert MillerArtemida Pharma Ltd, Stevenage, United Kingdom.
Jangsik ShinShin Poong Pharmaceutical Co, Ltd, Seoul, Korea.
Stephan DuparcMedicines for Malaria Venture (MMV), Geneva, Switzerland.
Umberto D'AlessandroDisease Control and Elimination Theme, Medical Research Council Unit, The Gambia at London School of Hygiene & Tropical Medicine, Fajara, The Gambia.
Christine ManyandoTropical Diseases Research Centre, Ndola, Zambia.
Jane AchanDisease Control and Elimination Theme, Medical Research Council Unit, The Gambia at London School of Hygiene & Tropical Medicine, Fajara, The Gambia.
MRC Unit the Gambia · GMTropical Diseases Research Centre · ZMMedicines for Malaria Venture · CHShin Poong Pharm (South Korea) · KR

Funding

Medical Research Council MC_UU_00026/1Shin Poong Pharmaceutical and Medicines for Malaria Venture
6 · The paper itself

Abstract

backgroundPyronaridine-artesunate (PA) is a registered artemisinin-based combination therapy, potentially useful for mass drug administration campaigns. However, further data are needed to evaluate its efficacy, safety and tolerability as full or incomplete treatment in asymptomatic Plasmodium falciparum-infected individuals.

methodsThis phase II, multi-center, open label, randomized clinical trial was conducted in The Gambia and Zambia. Participants with microscopically confirmed asymptomatic P. falciparum infection were randomly assigned (1:1:1) to receive a 3-day, 2-day, or 1-day treatment regimen of PA (180:60 mg), dosed according to bodyweight. The primary efficacy outcome was polymerase chain reaction (PCR)-adjusted adequate parasitological response (APR) at day 28 in the per-protocol population.

resultsA total of 303 participants were randomized. Day 28 PCR-adjusted APR was 100% for both the 3-day (98/98) and 2-day regimens (96/96), and 96.8% (89/94) for the 1-day regimen. Efficacy was maintained at 100% until day 63 for the 3-day and 2-day regimens but declined to 94.4% (84/89) with the 1-day regimen. Adverse event frequency was similar between the 3-day (51.5% [52/101]), 2-day (52.5% [52/99]), and 1-day (54.4% [56/103]) regimens; the majority of adverse events were of grade 1 or 2 severity (85% [136/160]). Asymptomatic, transient increases (>3 times the upper limit of normal) in alanine aminotransferase/aspartate aminotransferase were observed for 6/301 (2.0%) participants.

conclusionsPA had high efficacy and good tolerability in asymptomatic P. falciparum-infected individuals, with similar efficacy for the full 3-day and incomplete 2-day regimens. Although good adherence to the 3-day regimen should be encouraged, these results support the further investigation of PA for mass drug administration campaigns. CLINICAL TRIALS REGISTRATION: NCT03814616.

Indexed as

AntimalarialsMalariaMalaria, FalciparumArtesunateDrug CombinationsHumansNaphthyridinesPlasmodium falciparumTreatment OutcomeAntimalarialsArtesunateDrug CombinationsNaphthyridinespyronaridine tetraphosphate, artesunate drug combinationasymptomaticmalariapediatricpyronaridine-artesunaterandomized controlled clinical trial

Identifiers

PMID33983371
PMCPMC8800175
OpenAlexW3163383176

What OpenQuestion holds

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LicenceCC BY
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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.