Efficacy and Safety of the Anti-mucosal Addressin Cell Adhesion Molecule-1 Antibody Ontamalimab in Patients with Moderate-to-Severe Ulcerative Colitis or Crohn’s Disease

Author:

Vermeire Séverine1ORCID,Danese Silvio2ORCID,Sandborn William J3,Schreiber Stefan4,Hanauer Stephen5,D’Haens Geert6,Nagy Peter78ORCID,Thakur Manoj910,Bliss Caleb911,Cataldi Fabio912,Goetsch Martina713,Gorelick Kenneth J14,Reinisch Walter15ORCID

Affiliation:

1. Department of Gastroenterology & Hepatology, University Hospitals Leuven , Leuven , Belgium

2. Inflammatory Bowel Diseases Center, Department of Gastroenterology, Humanitas Clinical and Research Center–IRCSS, and Department of Biomedical Sciences, Humanitas University , Milan , Italy

3. Division of Gastroenterology, University of California San Diego , La Jolla, CA , USA

4. Department of General Internal Medicine, Christian-Albrechts-Universität , Kiel , Germany

5. Department of Medicine [Gastroenterology and Hepatology], Northwestern University Feinberg School of Medicine , Chicago, IL , USA

6. Department of Gastroenterology and Hepatology, Amsterdam UMC, University of Amsterdam , Amsterdam , The Netherlands

7. Shire, a Takeda company , Zug , Switzerland

8. Takeda Pharmaceuticals , Glattpark , Switzerland

9. Shire, a Takeda company , Lexington, MA , USA

10. Takeda Pharmaceuticals , Lexington, MA , USA

11. Apellis Pharmaceuticals , Waltham, MA , USA

12. Landos Biopharma , Blacksburg, VA , USA

13. Arena Pharmaceuticals, wholly owned subsidiary of Pfizer , Zurich , Switzerland

14. Zymo Consulting Group , Newtown Square, PA , USA

15. Department of Internal Medicine III, Division of Gastroenterology and Hepatology, Medical University of Vienna , Vienna , Austria

Abstract

Abstract Background and Aims Ontamalimab is a fully human immunoglobulin G2 monoclonal antibody against mucosal addressin cell adhesion molecule-1, developed as treatment for inflammatory bowel disease. Methods Six phase 3, multicentre, randomised, double-blind, placebo-controlled clinical trials compared efficacy and safety of ontamalimab [25 mg and 75 mg once every 4 weeks] with placebo in patients with moderate-to-severe ulcerative colitis or Crohn’s disease [two induction studies and one re-randomised maintenance study per condition]. This clinical trial programme was discontinued in 2020 for reasons unrelated to drug safety/efficacy; Crohn’s disease studies are described in the Supplementary data. Results The induction [12-week] and maintenance [52-week] studies included 659 and 366 randomised patients, respectively. More patients who received ontamalimab induction than placebo achieved the primary endpoint of clinical remission at Week 12 [25 mg, 18.5% vs 15.8%, p = 0.617, 27.0% vs 12.5%, p = 0.027; 75 mg, 29.8% vs 15.8%, p = 0.018, 29.5% vs 12.5% p = 0.014]; significantly more patients who received ontamalimab maintenance therapy than placebo achieved Week 52 clinical remission [25 mg, 53.5% vs 8.2%, p <0.001; 75 mg, 40.2% vs 12.8%, p <0.001]. Endoscopic improvement was generally significantly different vs placebo [induction: 25 mg, 27.8% vs 21.1%, p = 0.253, 35.1% vs 12.5%, p = 0.001; 75 mg, 41.1% vs 21.1%, p = 0.002, 33.9% vs 12.5%, p = 0.003; maintenance: 25 mg, 56.3% vs 9.6%, p <0.001; 75 mg, 48.8% vs 15.1%, p <0.001]. Adverse event rates were similar between ontamalimab and placebo groups. Conclusions Ontamalimab 75 mg was effective, with no safety concerns, as induction and maintenance therapy for patients with moderate-to-severe ulcerative colitis. [NCT03259334; NCT03259308; NCT03290781; NCT03559517; NCT03566823; NCT03627091]

Funder

Takeda Foundation

Publisher

Oxford University Press (OUP)

Subject

Gastroenterology,General Medicine

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