Evidence map›Paper›PMID 42458128›Full record

ArticleEuropean journal of clinical pharmacology2026

Unveiling the sumatriptan dose-relief relationship.

Clément Rigaut, Benoit Haut, Pierre Lambert, Jonathan Goole

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Article in European journal of clinical pharmacology, 2026. 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

4 authors.

Clément RigautTIPs (Transfers, Interfaces and Processes), Université libre de Bruxelles, Brussels, Belgium. clement.rigaut@ulb.be.ORCID https://orcid.org/0000-0003-4999-8601
Benoit HautTIPs (Transfers, Interfaces and Processes), Université libre de Bruxelles, Brussels, Belgium.
Pierre LambertTIPs (Transfers, Interfaces and Processes), Université libre de Bruxelles, Brussels, Belgium.
Jonathan GooleTherapeutic Chemistry department, Université libre de Bruxelles, Brussels, Belgium.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeThis article aims to correlate the pharmacokinetic parameters of sumatriptan to the percentage of patients experiencing relief after two hours.

methodsUsing data from the literature, a two-compartment pharmacokinetic model is developed to compute the concentration of sumatriptan in the brain across various routes of administration and doses. This concentration is then correlated to its clinical effect.

resultsThe maximum concentration of sumatriptan in the brain correlates linearly with the percentage of patients experiencing pain relief after two hours. Based on the evolution over time of the brain concentration, the action time can also be predicted for different route-dose combinations.

conclusionThe present correlation provides a relationship between the dose of sumatriptan and its effect for multiple routes of administration. The approach developed in this work could be adapted to other molecules to explore their dose-response relationships.

Indexed as

Migraine DisordersModels, BiologicalSerotonin 5-HT1 Receptor AgonistsSumatriptanBrainDose-Response Relationship, DrugHumansSerotonin 5-HT1 Receptor AgonistsSumatriptanConcentrationMigrainePharmacokineticsResponseTriptan

Identifiers

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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.