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Record W4414049491 · doi:10.1055/s-0045-1810779

Linerixibat significantly improves cholestatic pruritus in primary biliary cholangitis: results of the pivotal Phase 3 GLISTEN trial

2025· article· de· W4414049491 on OpenAlexaff
Gideon M. Hirschfield, Christopher L. Bowlus, D. I. Jones, Andreas E. Kremer, Marlyn J. Mayo, Atsushi Tanaka, Pietro Andreoné, Jidong Jia, Qinglong Jin, R U Macías-Rodríguez, Alexander R. Cobitz, Brooke M. Currie, Ciara Gorey, Igor Lazic, D.A. Podmore, Andrea Ribeiro, Jennifer B. Shannon, Brandon Swift, Megan McLaughlin, C Levy

Bibliographic record

VenueZeitschrift für Gastroenterologie · 2025
Typearticle
Languagede
FieldMedicine
TopicDrug Transport and Resistance Mechanisms
Canadian institutionsToronto General Hospital
Fundersnot available
KeywordsClinical trialPhase (matter)Primary (astronomy)Primary biliary cirrhosisBiliary tract

Abstract

fetched live from OpenAlex

Background and Aims: Cholestatic pruritus is common, debilitating and undertreated in patients with primary biliary cholangitis (PBC). Here, we describe the results of GLISTEN (NCT04950127), a Phase 3 study investigating the efficacy and safety of the ileal bile acid transporter inhibitor linerixibat for pruritus in PBC. Method: In this double-blind, randomised, placebo-controlled study, patients with PBC and moderate-to-severe pruritus received oral linerixibat 40 mg or placebo twice daily. Pruritus severity and pruritus-related sleep interference were assessed using a 0–10 numerical rating scale. The primary endpoint was change from baseline in worst itch over 24 weeks. Secondary endpoints included: at Week 2, change in worst itch; over 24 weeks, change in sleep interference; at Week 24, proportion of responders (≥2-,≥3,≥4-point reduction in worst itch). Safety endpoints included adverse event (AE) reporting. Results: 238 patients were randomised (95% females), itch severity was 7.34±1.54 (mean±standard deviation (SD)), 52% had alkaline phosphatase<1.67x upper limit of normal, and 47% were receiving stable therapy for pruritus. Pruritus improvement over 24 weeks was significantly greater with linerixibat than placebo: least-squares (LS) mean change -2.86 vs -2.15, adjusted mean difference -0.72; p=0.001. The effect of linerixibat was rapid and superior to placebo at Week 2: LS mean change -1.78 vs -1.07, adjusted mean difference -0.71; p<0.001. Linerixibat significantly improved pruritus-related sleep interference over 24 weeks vs placebo: LS mean change -2.77 vs -2.24, adjusted mean difference -0.53; p=0.024. At Week 24, more patients on linerixibat than placebo achieved a≥2-point (68% vs 64%),≥3-point (56% vs 43%) or≥4-point (41% vs 29%) reduction in pruritus. A higher proportion of linerixibat than placebo-treated patients reported their pruritus was very much improved (55% vs 37%) or absent (21% vs 9%). AEs reported more frequently with linerixibat than placebo were predominantly gastrointestinal (GI), including diarrhoea (61% vs 18%) and abdominal pain (18% vs 3%); 4% of patients in the linerixibat group discontinued treatment due to diarrhoea . Conclusion: In patients with PBC and moderate-to-severe pruritus, linerixibat rapidly and significantly improved pruritus and pruritus-related sleep interference vs placebo. While GI AEs were more common with linerixibat than placebo, they rarely led to treatment discontinuation. Funding: GSK Publication History Article published online: 04 September 2025 © 2025. Thieme. All rights reserved. Georg Thieme Verlag KG Oswald-Hesse-Straße 50, 70469 Stuttgart, Germany

Fetched live from OpenAlex and de-inverted. Abstracts are not stored in this database: the inverted indexes are 8.6 GB of the frame’s 9.3 GB of text, and the host has 13 GB free.

How this classification was reachedexpand

Full frame machine prediction

Teacher imitation

Not calibrated prevalence, not ground truth. Human validation pending. The Gemma side is a direct model label for every work in the frame, read from the title-only record. The Codex side is a classifier learned from the 10,348 direct Codex labels and calibrated to design-weighted sample rates; fields without enough sample support carry no Codex call. Candidate is the union of the two sides; consensus is their intersection. These outputs are machine_predicted_unvalidated and are not human labels.

metaresearch head score (Codex)0.001
metaresearch head score (Gemma)0.001
Version: metacan-v3-hybrid-931329e0061cValidation status: machine_predicted_unvalidated
Candidate categoriesnone
Consensus categoriesnone
DomainCandidate signal: none · Consensus signal: none
Study designCandidate signal: Randomized trial · Consensus signal: Randomized trial
GenreCandidate signal: Empirical · Consensus signal: Empirical
Teacher disagreement score0.003
Threshold uncertainty score0.011

Distilled classifier scores by category (both heads)

CategoryCodexGemma
Metaresearch0.0010.001
Meta-epidemiology (narrow)0.0010.000
Meta-epidemiology (broad)0.0020.001
Bibliometrics0.0000.000
Science and technology studies0.0000.000
Scholarly communication0.0010.001
Open science0.0000.000
Research integrity0.0010.002
Insufficient payload (model declined to judge)0.0030.001

Machine scores (provisional)

The two teacher heads of the student model, read on this work. A score orders the frame for review; it never asserts a category, and the validation status ships verbatim with every row.

Baseline scores from an immature model (maturity gate not passed, 7 training rounds). Scores rank; they never assert a category.

Opus teacher head0.013
GPT teacher head0.290
Teacher spread0.277 · how far apart the two teachers sit on this one work
Validation statusscore_only:v0-immature-baseline · verbatim from the scoring run: score_only means the number may rank works, and no category label ships from it

Classification

machine, unvalidated

Machine predicted; a candidate call from one source (direct Gemma or distilled Codex), not a consensus.

The models applied no category: nothing in the taxonomy fit this work.
Study designRandomized trial
Domainnot available
GenreEmpirical

How this classification was reached, model by model and score by score, is at the end of the page under "How this classification was reached".

Quick stats

Citations0
Published2025
Admission routes1
Has abstractno

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