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Record W4414049403 · doi:10.1055/s-0045-1810745

Etrasimod efficacy in patients with mildly to moderately active ulcerative colitis (modified Mayo score 4–6) in the phase 3 ELEVATE UC clinical programme

2025· article· en· W4414049403 on OpenAlexaff
Andrés Yarur, Geert D’Haens, Filip Baert, Martina Goetsch, Chuanbo Zang, G Gu, Roman Mazur, Michael J. Keating, Elizabeth M. Kudlacz, Shabir Sidhu, K Wosik, Silvio Danese

Bibliographic record

VenueZeitschrift für Gastroenterologie · 2025
Typearticle
Languageen
FieldBiochemistry, Genetics and Molecular Biology
TopicInflammatory Bowel Disease
Canadian institutionsPfizer (Canada)
Fundersnot available
KeywordsUlcerative colitisColitisClinical trialPhases of clinical researchPhase (matter)

Abstract

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Introduction: Etrasimod is an oral, once-daily (QD), selective sphingosine 1-phosphate (S1P) 1,4,5 receptor modulator for the treatment of moderately to severely active ulcerative colitis (UC). Objectives: To evaluate the efficacy and safety of etrasimod 2 mg QD vs placebo (PBO) in a subpopulation of patients (pts) from the ELEVATE UC clinical programme with mildly to moderately active UC at baseline (BL). Methodology: Data were pooled from the phase 3, randomised ELEVATE UC 52 (NCT03945188), ELEVATE UC 12 (NCT03996369) and ELEVATE UC 40 JAPAN (NCT04706793) trials [ 1 ] [ 2 ]. This post hoc analysis used a subset of pts aged≥18 years with a BL modified Mayo score (MMS) of 4–6 (with a centrally read endoscopic subscore≥2 and a rectal bleeding subscore [RBS]≥1). Efficacy endpoints at Week (Wk) 12 and Wk 52 included clinical remission, endoscopic improvement, symptomatic remission and endoscopic improvement-histologic remission (EIHR); at Wk 52, sustained clinical remission and corticosteroid (CS)-free clinical remission were assessed. Least square mean change from BL in pt-reported outcome 2 (PRO2) score (sum of RBS and stool frequency subscore) was assessed to Wk 52. Proportions of pts with treatment-emergent adverse events (TEAEs), serious TEAEs and TEAEs leading to discontinuation were assessed. Results: In this subgroup analysis, 221 pts received etrasimod and 109 received PBO. BL characteristics were generally balanced between treatment groups; 95 (28.8%) pts were taking CS at BL; 241 (73.0%) were biologic/Janus kinase inhibitor naïve. Median BL MMS was 6.0 in both treatment groups. Significantly greater proportions of pts receiving etrasimod vs PBO achieved all efficacy endpoints at Wk 12 and Wk 52 ([ Fig. 1 ]). A significant decrease in PRO2 score for etrasimod vs PBO was observed at Wk 2 and continued to Wk 32, with numerically greater score decreases from Wk 36 to Wk 52 ([ Table 1 ]). Safety was similar across treatment groups, and consistent with the overall ELEVATE UC population [ 1 ]. Fig. 1 Table 1 LS mean change from BL up to Wk 52 in PRO2 score in pts with mildly to moderately active UC (MMS 4–6) Pooled pt population a PBO QD, LS red (SE) [n] N=109 Etrasimod 2 mg QD, LS mean (SE) [n] N=221 LS mean difference (95% CI) p value Wk 2 -0.60 (0.134) [102] -1.06 (0.096) [212] -0.46 (-0.77, -0.15) 0.004 Wk 4 -0.89 (0.131) [104] -1.63 (0.094) [211] -0.74 (-1.04, -0.43) <0.001 Wk 8 -1.11 (0.137) [101] -1.89 (0.098) [205] -0.78 (-1.10, -0.46) <0.001 Wk 12 -1.12 (0.144) [95] -1.96 (0.102) [202] -0.84 (-1.18, -0.50) <0.001 Wk 16 -1.07 (0.216) [33] -1.90 (0.152) [101] -0.82 (-1.28, -0.37) <0.001 Wk 20 -1.07 (0.211) [34] -2.06 (0.147) [104] -0.99 (-1.43, -0.55) <0.001 Wk 24 -1.36 (0.213) [31] -1.99 (0.146) [102] -0.64 (-1.08, -0.19) 0.005 Wk 32 -1.31 (0.224) [29] -1.88 (0.148) [99] -0.57 (-1.04, -0.11) 0.017 Wk 40 -1.23 (0.265) [30] -1.71 (0.171) [95] -0.48 (-1.06, 0.09) 0.096 Wk 48 -1.30 (0.263) [27] -1.75 (0.167) [90] -0.45 (-1.02, 0.11) 0.116 Wk 52 -1.42 (0.249) [29] -1.90 (0.163) [89] -0.48 (-1.01, 0.05) 0.078 p <0.05 values are highlighted in bold. PRO2 score was defined as the sum of the RBS and SFS per individual protocol. Change from BL estimates are from an MMRM model that included BL score as a covariate and factors for study, naïve to biologic/Janus kinase inhibitor therapy at study entry (yes/no), BL CS use (yes/no), treatment, visit and the treatment by visit interaction. Data are as observed without imputation for missing values. a Data were pooled from ELEVATE UC 52 and ELEVATE UC 12 up to Wk 12, and from ELEVATE UC 52 and ELEVATE UC 40 JAPAN after Wk 12 up to Wk 52. BL, baseline; CI, confidence interval; CS, corticosteroid; LS, least squares; MMRM, mixed model for repeated measures; MMS, modified Mayo score; N, total number of patients per treatment group; n, number of patients with assessment at the specified visit; PBO, placebo; pt, patient; PRO2, patient-reported outcome 2; QD, once-daily; RBS, rectal bleeding subscore; SE, standard error; SFS, stool frequency subscore; UC, ulcerative colitis; Wk, Week. Conclusion: Etrasimod demonstrated robust efficacy in clinical, symptomatic and endoscopic endpoints and safety consistent with the overall population in pts with mildly to moderately active UC (MMS 4–6). Informationen zum Einsatz von KI : Pfizer's genAI tool MAIA assisted with 1st draft development; authors assume content responsibility. Publication History Article published online: 04 September 2025 © 2025. Thieme. All rights reserved. Georg Thieme Verlag KG Oswald-Hesse-Straße 50, 70469 Stuttgart, Germany

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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 score0.002
Threshold uncertainty score0.007

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 communication0.0010.000
Open science0.0000.000
Research integrity0.0010.001
Insufficient payload (model declined to judge)0.0010.000

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 head0.026
GPT teacher head0.332
Teacher spread0.306 · 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".

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Published2025
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