← Issue №2/ week of Jul 12, 2026/ the whole section, in full

IBD, in full.

All 1 IBD paper in this issue, as full cards, ranked by clinical utility. The issue page carries the strongest few; this is the section, whole.

Sections this issue
Filter

All 1, in full

most clinically useful first
IBD rct · n=137 · Jul 16, 2026 · Lancet GH · IF 30.9

Efficacy and safety of duvakitug in patients with ulcerative colitis (RELIEVE UCCD): a phase 2b, randomised, placebo-controlled trial.

New therapyulcerative colitisbiologicsanti-TNF
Clinical takeawayConsider duvakitug 900 mg every 2 weeks as a potential therapy for adults (18-75 years) with moderately to severely active ulcerative colitis, including those with prior inadequate response, loss of response, or intolerance to conventional or advanced therapies. Monitor for adverse events similarly to placebo.
What it foundDuvakitug 900 mg every 2 weeks achieved clinical remission (modified Mayo score ≤2 with no subscore >1) in 48% of patients vs 20% with placebo at week 14 (26% absolute difference, 95% CrI 8-44); 450 mg achieved 36% vs placebo (15% absolute difference, 95% CrI -3 to 33). Adverse events occurred in 43-49% of duvakitug patients vs 52% on placebo, with similar profiles.
ContextThis introduces a novel anti-TL1A monoclonal antibody with efficacy in a refractory population, though phase 3 confirmation is needed.
Emergingsuggested applicable standard· ACG Clinical Guideline Update: Ulcerative Colitis in Adults, Am J Gastroenterol 2025;120(6):1187-1224; AGA Living Guideline on Pharmacological Management of Moderate-to-Severe UC, Gastroenterology 2024 (panel review March 2026, no changes)

Decision at stakethe choice of advanced therapy for moderate to severe ulcerative colitis

Confirm ulcerative colitis with endoscopy showing continuous colonic inflammation from the rectum plus histology, after excluding infection with two-step CDI testing. Position advanced therapy by EFFICACY TIER, not by an anti-TNF-first rule.

From our summary of this standard, unedited — the part the paper bears on. marks omitted text. Our wording, not the guideline's; read the source for its own text.

Our full summary of this standard

Confirm ulcerative colitis with endoscopy showing continuous colonic inflammation from the rectum plus histology, after excluding infection with two-step CDI testing. Treat mild-moderate disease with 5-ASA by route and extent (suppository for proctitis, enema for left-sided, oral plus rectal for extensive); if 5-ASA fails, treat as moderate-to-severe rather than stepping up gradually. Position advanced therapy by EFFICACY TIER, not by an anti-TNF-first rule. Advanced-therapy-naive, higher efficacy: infliximab, vedolizumab, ozanimod, etrasimod, upadacitinib, risankizumab, guselkumab; intermediate: golimumab, ustekinumab, tofacitinib, filgotinib, mirikizumab; lower: adalimumab. PREVIOUSLY TNF-EXPOSED, higher efficacy: tofacitinib, upadacitinib, ustekinumab; lower: adalimumab, vedolizumab, ozanimod, etrasimod - S1P modulators are weakest in exactly this group. Do not cycle within the anti-TNF class after primary non-response; switch mechanism. Apply treat-to-target (STRIDE-II) to endoscopic improvement (MES 0-1). Screen for acute severe UC by Truelove-Witts and admit for IV steroids. Begin CRC surveillance 8-10 years after DIAGNOSIS for extensive or left-sided disease; isolated proctitis follows average-risk screening.

ACG Clinical Guideline Update: Ulcerative Colitis in Adults, Am J Gastroenterol 2025;120(6):1187-1224; AGA Living Guideline on Pharmacological Management of Moderate-to-Severe UC, Gastroenterology 2024 (panel review March 2026, no changes) ↗
Reinisch W … Jairath V · Lancet Gastroenterology & Hepatology · IF 30.9 · PubMed ↗Permalink
← Back to issue №2 Every section of this issue is one click away, at the top of this page. Follow IBD by RSS