Efficacy and Safety of Etrasimod in Patients with Moderately to Severely Active Isolated Proctitis: Results From the Phase 3 ELEVATE UC Clinical Programme.

S1P receptor modulator etrasimod proctitis

Journal

Journal of Crohn's & colitis
ISSN: 1876-4479
Titre abrégé: J Crohns Colitis
Pays: England
ID NLM: 101318676

Informations de publication

Date de publication:
13 Apr 2024
Historique:
received: 06 11 2023
medline: 13 4 2024
pubmed: 13 4 2024
entrez: 13 4 2024
Statut: aheadofprint

Résumé

Pivotal trials in ulcerative colitis have historically excluded patients with isolated proctitis. Etrasimod is an oral, oncedaily, selective sphingosine 1phosphate1,4,5 receptor modulator for the treatment of moderately to severely active ulcerative colitis. This post hoc analysis assessed efficacy and safety of etrasimod 2 mg once daily in patients with isolated proctitis (centrally read) from the phase 3 ELEVATE UC 52 and ELEVATE UC 12 trials. Patients, including those with isolated proctitis (<10 cm rectal involvement) who met all other inclusion criteria in ELEVATE UC 52 and ELEVATE UC 12, were randomised 2:1 to receive etrasimod or placebo. Primary, secondary and other identified efficacy endpoints and safety were assessed. We analysed data from 64 and 723 patients at Week 12 (both trials pooled), and 36 and 397 patients at Week 52 (ELEVATE UC 52 only) with isolated proctitis and more extensive colitis (≥10 cm rectal involvement), respectively. Patients with isolated proctitis receiving etrasimod demonstrated significant improvements versus placebo, including clinical remission rates at Weeks 12 (42.9% vs 13.6%) and 52 (44.4% vs 11.1%), endoscopic improvement (52.4% vs 22.7%) at Week 12 and bowel urgency numerical rating scale score at Week 12 (all p<0.01). Generally similar trends were observed in patients with more extensive colitis. Safety was consistent across subgroups, with no new findings. Etrasimod demonstrated significant improvements versus placebo in patients with isolated proctitis, and those with more extensive disease, in most efficacy endpoints at Week 12 and 52.

Sections du résumé

BACKGROUND AND AIMS OBJECTIVE
Pivotal trials in ulcerative colitis have historically excluded patients with isolated proctitis. Etrasimod is an oral, oncedaily, selective sphingosine 1phosphate1,4,5 receptor modulator for the treatment of moderately to severely active ulcerative colitis. This post hoc analysis assessed efficacy and safety of etrasimod 2 mg once daily in patients with isolated proctitis (centrally read) from the phase 3 ELEVATE UC 52 and ELEVATE UC 12 trials.
METHODS METHODS
Patients, including those with isolated proctitis (<10 cm rectal involvement) who met all other inclusion criteria in ELEVATE UC 52 and ELEVATE UC 12, were randomised 2:1 to receive etrasimod or placebo. Primary, secondary and other identified efficacy endpoints and safety were assessed.
RESULTS RESULTS
We analysed data from 64 and 723 patients at Week 12 (both trials pooled), and 36 and 397 patients at Week 52 (ELEVATE UC 52 only) with isolated proctitis and more extensive colitis (≥10 cm rectal involvement), respectively. Patients with isolated proctitis receiving etrasimod demonstrated significant improvements versus placebo, including clinical remission rates at Weeks 12 (42.9% vs 13.6%) and 52 (44.4% vs 11.1%), endoscopic improvement (52.4% vs 22.7%) at Week 12 and bowel urgency numerical rating scale score at Week 12 (all p<0.01). Generally similar trends were observed in patients with more extensive colitis. Safety was consistent across subgroups, with no new findings.
CONCLUSIONS CONCLUSIONS
Etrasimod demonstrated significant improvements versus placebo in patients with isolated proctitis, and those with more extensive disease, in most efficacy endpoints at Week 12 and 52.

Identifiants

pubmed: 38613425
pii: 7645267
doi: 10.1093/ecco-jcc/jjae038
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Informations de copyright

© The Author(s) 2024. Published by Oxford University Press on behalf of European Crohn’s and Colitis Organisation. All rights reserved. For commercial re-use, please contact reprints@oup.com for reprints and translation rights for reprints. All other permissions can be obtained through our RightsLink service via the Permissions link on the article page on our site—for further information please contact journals.permissions@oup.com.

Auteurs

Laurent Peyrin-Biroulet (L)

Department of Gastroenterology, Nancy University Hospital, F-54500 Vandœuvre-lès-Nancy, France.
INSERM, NGERE, University of Lorraine, F-54000 Nancy, France.
INFINY Institute, Nancy University Hospital, F-54500 Vandœuvre-lès-Nancy, France.
FHU-CURE, Nancy University Hospital, F-54500 Vandœuvre-lès-Nancy, France.
Groupe Hospitalier privé Ambroise Paré - Hartmann, Paris IBD Center, 92200 Neuilly sur Seine, France.
Division of Gastroenterology and Hepatology, McGill University Health Centre, Montreal, QC, Canada.

Marla C Dubinsky (MC)

Susan and Leonard Feinstein IBD Center, Icahn School of Medicine at Mount Sinai, New York, NY, USA.

Bruce E Sands (BE)

Dr. Henry D. Janowitz Division of Gastroenterology, Icahn School of Medicine at Mount Sinai, New York, NY, USA.

Julian Panés (J)

Formerly Department of Gastroenterology, Hospital Clínic de Barcelona, IDIBAPS, CIBERehd, Barcelona, Spain.

Stefan Schreiber (S)

Department of Internal Medicine I, University Hospital Schleswig-Holstein, Kiel University, Kiel, Germany.

Walter Reinisch (W)

Department of Internal Medicine III, Medical University of Vienna, Vienna, Austria.

Brian G Feagan (BG)

Division of Gastroenterology, Department of Medicine, Western University, London, ON, Canada.
Alimentiv Inc, London, ON, Canada.

Silvio Danese (S)

Division of Gastroenterology and Endoscopy, IRCCS San Raffaele Hospital and Vita Salute San Raffaele University, Milan, Italy.

Andres J Yarur (AJ)

Inflammatory Bowel Disease Center and Division of Gastroenterology and Hepatology, Cedars-Sinai Medical Center, Los Angeles, CA, USA.

Geert R D'Haens (GR)

Department of Gastroenterology and Hepatology, Amsterdam University Medical Centers, Amsterdam, The Netherlands.

Martina Goetsch (M)

Pfizer AG, Zürich, Switzerland.

Karolina Wosik (K)

Pfizer Inc, Kirkland, QC, Canada.

Michael Keating (M)

Pfizer Inc, New York, NY, USA.

Krisztina Lazin (K)

Pfizer AG, Zürich, Switzerland.

Joseph Wu (J)

Pfizer Inc, Cambridge, MA, USA.

Irene Modesto (I)

Pfizer Inc, New York, NY, USA.

Aoibhinn McDonnell (A)

Pfizer Ltd, Sandwich, Kent, UK.

Lauren Bartolome (L)

Pfizer Inc, New York, NY, USA.

Séverine Vermeire (S)

Department of Gastroenterology and Hepatology, University Hospitals Leuven, Leuven, Belgium.

Classifications MeSH