Symptomatic relief (post hoc analysis)

Patients on ZEPOSIA achieved rapid symptomatic relief one week after
completing the 7-day dose titration (post hoc analysis)¹

Symptomatic response* in the
TRUE NORTH induction period^†

Adapted from Siegmund B et al. 2022.¹

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Patients on ZEPOSIA achieved higher rates of symptomatic remission vs placebo as early as Week 5 after treatment initiation (post hoc analysis)¹

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Adapted from Siegmund B et al. 2022.¹

*Symptomatic response was defined as a decrease from baseline of ≥1 point and ≥30% in the adapted partial Mayo score (sum of the RBS, SFS, and Physician Global Assessment subscore, ranging from 0–9 points) and a decrease of ≥1 point from baseline in RBS or an absolute RBS ≤1 point.¹
^†Data are based on the non-responder imputation.¹
^‡Symptomatic remission was defined as a RBS of 0 points and a SFS ≤1 point (and a decrease of ≥1 point from the baseline SFS).¹

CI, confidence interval; RBS, rectal-bleeding subscore; SFS, stool-frequency subscore.

Reference

Siegmund B et al. Poster presented at: European Crohn’s and Colitis Organisation, Virtual; 16–19 February, 2022. Poster: DOP43.

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Legal Notice | Privacy Policy

Adverse events should be reported. Reporting forms and information can be found at: UK – www.mhra.gov.uk/yellowcard, or search for MHRA Yellow Card in the Google Play or Apple App Store. Ireland-via HPRA Pharmacovigilance at www.hpra.ie Adverse events should also be reported to Bristol-Myers Squibb via medical.information@bms.com or 0800 731 1736 (UK); 1800 749 749 (Ireland).

Symptomatic relief (post hoc analysis)

Symptomatic relief (post hoc analysis)

Patients on ZEPOSIA achieved rapid symptomatic relief one week after completing the 7-day dose titration (post hoc analysis)1

Symptomatic response* in the TRUE NORTH induction period†

Patients on ZEPOSIA achieved higher rates of symptomatic remission vs placebo as early as Week 5 after treatment initiation ​(post hoc analysis)1

Reference

Patients on ZEPOSIA achieved rapid symptomatic relief one week after
completing the 7-day dose titration (post hoc analysis)¹

Symptomatic response* in the
TRUE NORTH induction period^†

Patients on ZEPOSIA achieved higher rates of symptomatic remission vs placebo as early as Week 5 after treatment initiation (post hoc analysis)¹