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the REMONO-CD and the REMONO-UC Studies
Sponsor: University Hospital, Clermont-Ferrand
Summary
Infliximab was the first-in-class anti-TNF agent approved for treating patients with IBD, both for Crohn's disease (CD)1 and ulcerative colitis (UC)2. Infliximab is administered by intravenous infusions and demonstrated its superiority over placebo to induce and maintain steroid-free clinical remission. Besides, SONIC and SUCCESS trials showed that combination therapy (infliximab + immunosuppressant) was more effective than infliximab alone to induce clinical remission3,4. Moreover, the PANTS cohort confirmed the benefits of combination therapy to induce remission and to prevent immunogenicity over time5. Accordingly, current guidelines recommend to use infliximab in combination with an immunosuppressive therapy. Recently, subcutaneous (SC) infliximab has been developed and is now approved for patients with CD and UC6. The LIBERTY-CD and LIBERTY-UC trials showed that SC infliximab is more effective than placebo to maintain clinical remission7. Real-world evidence studies, such as the REMSWITCH program8,9, reported that switching from IV to SC infliximab is feasible, safe and well accepted leading to a low risk of relapse including in patients with intensified IV doses. In addition to its better acceptability compared to IV regimen, SC infliximab seems to have a better pharmacokinetic profile that can lead to reduced risk of immunogenicity and thus question the need for using combination therapy with SC infliximab6-9. No data enables to draw any firm conclusion on this topic10. In the REMONO studies (REMONO-UC and REMONO-CD), we aim to show the non-inferiority of SC infliximab monotherapy to maintain steroid-free clinical remission compared to combination therapy in patients with CD and UC.
Official title: Non-inferiority REal-world Evidence Study Comparing the Effectiveness of Subcutaneous Infliximab MONOtherapy and Subcutaneous Infliximab Combined With Immunosuppressive Therapy in Patients With Crohn's Disease and Ulcerative Colitis.
Key Details
Gender
All
Age Range
18 Years - Any
Study Type
OBSERVATIONAL
Enrollment
420
Start Date
2025-08-01
Completion Date
2026-10
Last Updated
2026-05-04
Healthy Volunteers
No
Locations (18)
CHU Amiens
Amiens, France
CHU Besançon
Besançon, France
CHU Clermont Ferrand
Clermont-Ferrand, France
Hôpital Beaujon AP-HP
Clichy, France
Hôpital Henri-Mondor AP-HP
Créteil, France
CHU Dijon
Dijon, France
CHU Grenoble
Grenoble, France
Hôpital Bicêtre AP-HP
Le Kremlin-Bicêtre, France
CHU Lille
Lille, France
Hospice Civil de Lyon
Lyon, France
Hôpital Henri-Mondor AP-HP
Marseille, France
CHU Monptellier
Montpellier, France
CHU Nancy
Nancy, France
CHU Nantes
Nantes, France
Institut des MICI
Neuilly-sur-Seine, France
CHU Nîmes
Nîmes, France
CHU Rouen
Rouen, France
CHU Toulouse
Toulouse, France