Evidence map›Paper›PMID 38840151›Full record

Trial reportMalaria journal2024

Bioequivalence of a new coated 15 mg primaquine formulation for malaria elimination.

Julie Nguyen Ngoc Pouplin, Thoopmanee Kaendiao, Bilal Ahmad Rahimi, Mayur Soni, Hensi Basopia, Darshana Shah, Jitendra Patil, Vyom Dholakia, Yash Suthar, Joel Tarning and 2 more

Abstract readRandomized Controlled Trial
In one paragraph

Trial report in Malaria journal, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

12 authors.

Julie Nguyen Ngoc PouplinRéseau Médicaments et Développement, 21Bis Avenue du Commandant l'Herminier, 44600, Saint-Nazaire, France. julie.nguyen@remed.org.
Thoopmanee KaendiaoMahidol Oxford Tropical Medicine Clinical Research Unit, Mahidol University, Bangkok, Thailand.
Bilal Ahmad RahimiDepartment of Paediatrics, Faculty of Medicine, Kandahar University, Kandahar, Afghanistan.
Mayur SoniCliantha Research Limited, Cliantha Corporate, Ahmedabad, Gujarat, India.
Hensi BasopiaCliantha Research Limited, Cliantha Corporate, Ahmedabad, Gujarat, India.
Darshana ShahCliantha Research Limited, Cliantha Corporate, Ahmedabad, Gujarat, India.
Jitendra PatilCliantha Research Limited, Cliantha Corporate, Ahmedabad, Gujarat, India.
Vyom DholakiaCliantha Research Limited, Cliantha Corporate, Ahmedabad, Gujarat, India.
Yash SutharCliantha Research Limited, Cliantha Corporate, Ahmedabad, Gujarat, India.
Joel TarningMahidol Oxford Tropical Medicine Clinical Research Unit, Mahidol University, Bangkok, Thailand.
Mavuto MukakaMahidol Oxford Tropical Medicine Clinical Research Unit, Mahidol University, Bangkok, Thailand.
Walter R TaylorMahidol Oxford Tropical Medicine Clinical Research Unit, Mahidol University, Bangkok, Thailand.

Funding

MRC MR/V027522/1Wellcome Trust
6 · The paper itself

Abstract

backgroundWith only one 15 mg primaquine tablet registered by a stringent regulatory authority and marketed, more quality-assured primaquine is needed to meet the demands of malaria elimination.

methodsA classic, two sequence, crossover study, with a 10-day wash out period, of 15 mg of IPCA-produced test primaquine tablets and 15 mg of Sanofi reference primaquine tablets was conducted. Healthy volunteers, aged 18-45 years, without glucose-6-phosphate dehydrogenase deficiency, a baseline haemoglobin ≥ 11 g/dL, creatinine clearance ≥ 70 mL/min/1.73 ms, and body mass index of 18.5-30 kg/m

results47 of 50 volunteers, median age 33 years, completed both dosing rounds and were included in the bioequivalence analysis. For primaquine, GM C

conclusionIPCA primaquine was bioequivalent to the Sanofi primaquine. This opens the door to prequalification, registration in malaria endemic countries, and programmatic use for malaria elimination. Trial registration The trial registration reference is ISRCTN 54640699.

Indexed as

AntimalarialsCross-Over StudiesPrimaquineTherapeutic EquivalencyAdolescentAdultFemaleHealthy VolunteersHumansMalariaMaleMiddle AgedTabletsYoung AdultAntimalarialsPrimaquineTabletsBioequivalenceMalariaPharmacokineticsPrimaquine

Identifiers

PMID38840151
PMCPMC11155120

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Registered trials

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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.