Evidence map›Paper›PMID 38563414›Full record

ArticleClinical and translational science2024

Pharmacokinetics, pharmacodynamics, and safety of fesomersen, a novel antisense inhibitor of factor XI, in healthy Chinese, Japanese, and Caucasian volunteers.

Tianxing Liu, Kensei Hashizume, Eva Krieg, Huijun Chen, Yuki Mukaida, Kirstin Thelen, Frauke Friedrichs, Stefan Willmann, Stephan Schwers, Alexander Solms and 1 more

Open access · goldAbstract read
In one paragraph

Article in Clinical and translational science, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
5.3field-weighted citation impact, top 4% 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.

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

8 citing papers in PubMed, 12 citations in OpenAlex.

  1. Review
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  5. RNA therapeutics in cardiovascular medicine.Current opinion in cardiology · 2025
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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

11 authors at 4 institutions in 4 countries.

Tianxing LiuResearch & Development, Pharmaceuticals, Bayer AG, Beijing, China.ORCID 0009-0004-3462-2163
Kensei HashizumeResearch & Development Japan, Bayer Yakuhin, Ltd., Tokyo, Japan.ORCID 0009-0001-6922-6548
Eva KriegResearch & Development, Pharmaceuticals, Bayer AG, Wuppertal/Leverkusen/Berlin, Germany.ORCID 0009-0005-8113-9710
Huijun ChenResearch & Development, Pharmaceuticals, Bayer AG, Beijing, China.ORCID 0000-0003-0268-2976
Yuki MukaidaResearch & Development Japan, Bayer Yakuhin, Ltd., Tokyo, Japan.ORCID 0009-0009-9895-8391
Kirstin ThelenResearch & Development, Pharmaceuticals, Bayer AG, Wuppertal/Leverkusen/Berlin, Germany.
Frauke FriedrichsResearch & Development, Pharmaceuticals, Bayer AG, Wuppertal/Leverkusen/Berlin, Germany.ORCID 0009-0002-7005-8964
Stefan WillmannResearch & Development, Pharmaceuticals, Bayer AG, Wuppertal/Leverkusen/Berlin, Germany.ORCID 0000-0001-8322-965X
Stephan SchwersResearch & Development, Pharmaceuticals, Bayer AG, Wuppertal/Leverkusen/Berlin, Germany.ORCID 0000-0001-7038-6197
Alexander SolmsResearch & Development, Pharmaceuticals, Bayer AG, Wuppertal/Leverkusen/Berlin, Germany.ORCID 0000-0002-0945-2543
Rosie YuIonis Pharmaceuticals, Inc., Carlsbad, California, USA.
Bayer (Germany) · DEBayer (China) · CNBayer (Japan) · JPIonis Pharmaceuticals (United States) · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The inhibition of coagulation factor XI (FXI) presents an attractive approach for anticoagulation as it is not expected to increase the risk of clinically relevant bleeding and is anticipated to be at least as effective as currently available anticoagulants. Fesomersen is a conjugated antisense oligonucleotide that selectively inhibits the expression of FXI. The article describes three clinical studies that investigated the safety, pharmacokinetic (PK), and pharmacodynamic (PD) profiles of fesomersen after subcutaneous (s.c.) injection to healthy participants. The studies included participants from diverse ethnic backgrounds (Caucasian, Japanese, and Chinese). Fesomersen demonstrated good safety and tolerability in all three studies. No major bleeding events were observed. After single-dose s.c. injection, fesomersen was rapidly absorbed into the systemic circulation, with maximum fesomersen-equivalent (fesomersen-eq) concentrations (C

Indexed as

Factor XIHemorrhageDose-Response Relationship, DrugDouble-Blind MethodEast Asian PeopleHealthy VolunteersHumansPartial Thromboplastin TimeWhite PeopleFactor XI

Identifiers

PMID38563414
PMCPMC10985948
OpenAlexW4393411546

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
Read underepoch 390

Registered trials

None linked

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.