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New SKYRIZI and RINVOQ data show disease control in inflammatory bowel disease

New data from pharmaceutical research suggest that two medicines, SKYRIZI (risankizumab) and RINVOQ (upadacitinib), may help people with inflammatory bowel disease, including Crohn’s disease, achieve better disease control. The findings come from phase 3 studies and real-world observations presented at a major gastroenterology meeting, and they may affect treatment options for patients who have not had satisfactory control with other therapies.

What the new data show

The new phase 3AFFIRM data indicate higher rates of clinical and endoscopic response for Crohn’s disease patients treated with subcutaneous SKYRIZI compared with placebo across multiple efficacy endpoints. Open-label extension analyses suggest sustained endoscopic improvements over time, even for patients with more complex disease and prior treatments. Real-world observations point to disease control with RINVOQ in advanced Crohn’s disease, suggesting potential benefits for patients who are hard to treat. These results were presented in the context of discussions at the American College of Gastroenterology 2026 Annual Scientific Meeting.

Key facts explained in plain terms

Who could be affected

People living with Crohn’s disease or other inflammatory bowel diseases who have not achieved adequate control with current therapies might be candidates for SKYRIZI or RINVOQ based on the reported data. The new results emphasize potential options for patients who have tried multiple medicines without satisfactory results, though decisions depend on individual medical history and physician judgment.

Practical next steps for patients and clinicians

Limits of the current data and questions to monitor

The explainer summarizes data reported at a scientific meeting and from open-label extensions; such presentations are not the same as final regulatory approvals or long-term, real-world registries. Further peer-reviewed publication and regulatory review are needed to confirm results and determine exact clinical roles. Clinicians will weigh individual risk-benefit for each patient and may require additional safety monitoring.

Which sources did Setup in Bahrain review?

Setup in Bahrain reviewed the following source material before preparing this explanatory article.

The links remain visible so readers can inspect the evidence, compare dates and context, and confirm current requirements with the relevant authority.

Information and responsibility notice: This article is general information based on the cited material available when published. It is not legal, tax, immigration, medical, financial, banking, or investment advice; it does not create a professional-client relationship; and it is not a guarantee of outcome, availability, accuracy, or eligibility. Rules, schedules, prices, and third-party information can change. Confirm material decisions with the relevant authority and an appropriately qualified adviser before acting.

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