Evidence map›Paper›PMID 41567011›Full record

ArticleClinical and translational science2026

Quantitative Prediction of Human Pharmacokinetics for Fc-Engineered Therapeutic Monoclonal Antibodies With Increased FcRn Binding Mutations After Subcutaneous Injection.

Kenta Haraya, Taichi Kuramochi

Abstract read
In one paragraph

Article in Clinical and translational science, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Article
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

2 authors.

Kenta HarayaResearch Division, Chugai Pharmaceutical Co., Ltd, Yokohama, Kanagawa, Japan.ORCID 0000-0002-9142-5607
Taichi KuramochiResearch Division, Chugai Pharmaceutical Co., Ltd, Yokohama, Kanagawa, Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Fc-engineered antibodies (mAbs) enhancing FcRn binding have rapidly expanded in drug discovery and development. Although an approach exists for predicting the pharmacokinetics of Fc-engineered mAbs after intravenous injections in humans, no methodology has been established for predicting pharmacokinetics after subcutaneous injections. This study aimed to establish a methodology for predicting the pharmacokinetics of Fc-engineered mAbs after subcutaneous injections in humans. First, bioavailability (F) and absorption rate constant (k

Indexed as

Antibodies, MonoclonalHistocompatibility Antigens Class IImmunoglobulin Fc FragmentsReceptors, FcAnimalsArea Under CurveBiological AvailabilityHumansInjections, SubcutaneousMacaca fascicularisMaleModels, BiologicalMutationProtein BindingProtein EngineeringAntibodies, MonoclonalFc receptor, neonatalHistocompatibility Antigens Class IImmunoglobulin Fc FragmentsReceptors, Fcallometric scalingcynomolgus monkeyFc‐engineered mAbsFcRnpharmacokineticssubcutaneous

Identifiers

PMID41567011
PMCPMC12824526

What OpenQuestion 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 OpenQuestion graph.