Evidence mapPaperPMID 42474239Full record

Trial reportClinical pharmacology in drug development2026

Comparative bioavailability of a novel fixed-dose combination of ticagrelor and acetylsalicylic acid.

Susana Tera-Ponce, Perla E Castañeda-Tera, Elva J García-Real, Francisco Ávila-García, Kevin F Rios-Brito, Laura A Lugo-Sánchez, Daniel E Sandoval-Colin, Paola M Medina-Cárdenas, Jorge González-Canudas

Abstract readRandomized Controlled TrialComparative Study
In one paragraph

Trial report in Clinical pharmacology in drug development, 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

9 authors.

Susana Tera-PonceDepartment of Pharmacology, Faculty of Medicine, National Autonomous University of Mexico (UNAM), Mexico City, Mexico.
Perla E Castañeda-TeraUnidad Clínica Farmacológica Bioemagno, S. A. de C. V, Mexico City, Mexico.
Elva J García-RealUnidad Clínica Farmacológica Bioemagno, S. A. de C. V, Mexico City, Mexico.
Francisco Ávila-GarcíaBioanalit Laboratorios, S.A. de C.V, Mexico City, Mexico.
Kevin F Rios-BritoResearch and Development Department, Laboratorios Silanes S.A. de C.V., Mexico City, Mexico.
Laura A Lugo-SánchezResearch and Development Department, Laboratorios Silanes S.A. de C.V., Mexico City, Mexico.
Daniel E Sandoval-ColinResearch and Development Department, Laboratorios Silanes S.A. de C.V., Mexico City, Mexico.
Paola M Medina-CárdenasResearch and Development Department, Laboratorios Silanes S.A. de C.V., Mexico City, Mexico.
Jorge González-CanudasResearch and Development Department, Laboratorios Silanes S.A. de C.V., Mexico City, Mexico.

Funding

Laboratorios Silanes, S.A. de C.V.
6 · The paper itself

Abstract

Dual antiplatelet therapy (DAPT) with acetylsalicylic acid (hereafter referred to as ASA) and ticagrelor is the standard of care for secondary prevention for atherothrombotic events, particularly in patients with noncardioembolic cerebrovascular disease or coronary artery disease. However, prolonged DAPT requires multiple daily tablets, which can compromise adherence; a fixed-dose combination could reduce pill burden and improve treatment persistence. This study evaluated the comparative bioavailability of a fixed-dose combination (FDC) capsule of ticagrelor 90 mg/ASA 100 mg (test) versus the concomitant administration of ticagrelor 90 mg tablet plus ASA 100 mg tablet (reference) under fasting conditions in healthy Mexican volunteers. We applied a randomized, open-label, two-period crossover, single-dose design with a 7-day washout and quantified plasma concentrations by liquid chromatography-tandem mass spectrometry. Twenty-four subjects were enrolled. Geometric mean ratios (90% confidence intervals) for ticagrelor maximum plasma concentration and area under the plasma concentration-time curve from 0 to 48 h, were 111.5% (102.3-121.5), and 100.3% (93.4-107.7); for salicylic acid, 95.4% (90.1-100.9), and 101.5% (96.7-106.5). All 90% confidence intervals fell within the predefined 80-125% range, and both formulations were well tolerated. These findings support the FDC as an alternative that may simplify long-term DAPT for the secondary prevention of atherothrombotic events.

Indexed as

AspirinPlatelet Aggregation InhibitorsTicagrelorAdultArea Under CurveBiological AvailabilityCapsulesCross-Over StudiesDrug CombinationsFemaleHealthy VolunteersHumansMaleMexicoTabletsTandem Mass SpectrometryAspirinCapsulesDrug CombinationsPlatelet Aggregation InhibitorsTabletsTicagreloracetylsalicylic acidcomparative bioavailabilitydual antiplatelet therapyfixed‐dose combinationhealthy Mexican volunteerspharmacokineticsticagrelor

Identifiers

PMID42474239
PMCPMC13383814

What Socratic holds

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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 Socratic graph.