ECCO 2024 Symposium – Early Action, Major Impact: S1Ps for the Moderate Ulcerative Colitis Patient - European Medical Journal

ECCO 2024 Symposium – Early Action, Major Impact: S1Ps for the Moderate Ulcerative Colitis Patient

Gastroenterology

This information is for Healthcare Professionals only.

These promotional video was organised and funded by Bristol Myers Squibb. BMS medicines and/or production information may be discussed.


Click here for Prescribing Information

This BMS-sponsored promotional symposium, presented at the European Crohn’s and Colitis Organisation (ECCO) Congress 2024, presents a thought-provoking view on the latest developments in therapeutic modalities for ulcerative colitis (UC).

‘Early Action, Major Impact: S1Ps for the Moderate Ulcerative Colitis Patient’ highlights the broad spectrum of therapeutic modalities within the current treatment landscape in managing patients progressing to moderate-to-severe UC, and reviews the latest data from clinical studies of S1P receptor modulators.

Prof. Remo Panaccione and Prof. Marla Dubinksy address the current limitations of traditional UC treatments and the importance of early intervention in the disease course. Discussion continues to reflect on the positioning of S1P receptor modulators early in the treatment algorithm.

Prof. James Lindsay reviews the latest clinical trials and real-world evidence of S1P receptor modulators including the 4-year data from the TRUE NORTH OLE1 trial which evaluates the long-term efficacy and safety data of ozanimod of patients with moderate-to-severe UC.

Job code: IMM-GB-2400112

Date of Prep: April 2024

Ozanimod is indicated for the treatment of adult patients with moderately-to-severely active UC who have had an inadequate response, lost response, or were intolerant to either conventional therapy or a biologic agent.

Click here to view ECCO 2023 Symposium – Multidisciplinary Perspectives in UC: A Closer Look at S1P Receptor Modulators

Adverse events should be reported. Reporting forms and information can be found via: Great Britain & Northern Ireland – The Yellow Card Scheme at: www.mhra.gov.uk/yellowcard or search for MHRA Yellow Card in the Goggle Play or Apple App store; Ireland – HPRA Pharmacovigilance at www.hpra.ie. Adverse events should also be reported to Bristol-Myers Squibb via [email protected] or 08007311736 (Great Britain & Northern Ireland); 1 800 749 749 (Ireland).

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