Maintenance Risankizumab Sustains Induction Response in Patients with Crohn’s Disease in a Randomized Phase 3 Trial

Author:

Ferrante Marc1ORCID,Irving Peter M2ORCID,Abreu Maria T3,Axler Jeffrey4,Gao Xiang5,Cao Qian6,Fujii Toshimitsu7,Rausch Astrid8,Torres Joana91011ORCID,Neimark Ezequiel12,Song Alexandra12,Wallace Kori12,Kligys Kristina12,Berg Sofie12,Liao Xiaomei12,Zhou Qing12,Kalabic Jasmina13,Feagan Brian14,Panaccione Remo15ORCID

Affiliation:

1. Department of Gastroenterology and Hepatology, University Hospitals Leuven, KU Leuven , Leuven , Belgium

2. IBD Centre, Guy’s and St Thomas’ NHS Foundation Trust , London , UK

3. University of Miami Miller School of Medicine , Miami, FL , USA

4. Toronto Digestive Disease Associates Inc. , Vaughan, ON , Canada

5. Department of Gastroenterology, The Center for Inflammatory Bowel Disease, The Sixth Affiliated Hospital, Sun Yat-sen University , Guangzhou, Guangdong , China

6. Department of Gastroenterology, Sir Run Run Shaw Hospital, Zhejiang University School of Medicine , Hangzhou, Zhejiang , China

7. Department of Gastroenterology and Hepatology, Tokyo Medical and Dental University , Tokyo , Japan

8. Gastroenterology Department, British Hospital , Buenos Aires , Argentina

9. Division of Gastroenterology, Hospital Beatriz Ângelo , Loures , Portugal

10. Hospital da Luz , Lisbon , Portugal

11. Faculdade de Medicina, Universidade de Lisboa , Lisbon , Portugal

12. AbbVie Inc. , North Chicago, IL , USA

13. AbbVie Deutschland GmbH & Co. KG , Ludwigshafen , Germany

14. University of Western Ontario , London, ON , Canada

15. Division of Gastroenterology and Hepatology, Cumming School of Medicine, University of Calgary , Calgary, AB , Canada

Abstract

Abstract Background and Aims Durable clinical remission, endoscopic healing, and biomarker normalization are key treatment goals for Crohn’s disease. The selective anti-interleukin-23 p19 inhibitor risankizumab has demonstrated efficacy and safety in moderately to severely active Crohn’s disease. This post-hoc analysis of data from the pivotal risankizumab maintenance study assessed whether risankizumab maintenance therapy sustained the clinical and endoscopic outcomes achieved with risankizumab induction therapy. Methods We evaluated 462 patients who achieved a clinical response to risankizumab intravenous induction treatment and were re-randomized to receive subcutaneous risankizumab 360 mg, subcutaneous risankizumab 180 mg, or placebo [withdrawal] every 8 weeks for 52 weeks in the randomized, controlled FORTIFY maintenance study. Maintenance of clinical, endoscopic, and biomarker endpoints at week 52 among patients who achieved these endpoints after 12 weeks of induction treatment was evaluated. Results A significantly higher proportion of patients receiving maintenance treatment with risankizumab 360 or 180 mg compared with placebo [withdrawal] maintained Crohn’s Disease Activity Index remission [68.6%, 70.8%, vs 56.3%; p < 0.05], stool frequency/abdominal pain remission [69.2%, 64.1%, vs 50.5%; p < 0.01], endoscopic response [70.2%, 68.2%, vs 38.4%; p < 0.001], endoscopic remission [74.4%, 45.5%, vs 23.9%; p < 0.05], and Simple Endoscopic Score for Crohn’s Disease of 0–2 [65.5%, 36.7%, vs 21.9%]. Most patients [56.8–83.3%] who achieved normalized faecal calprotectin or C-reactive protein during induction sustained them with maintenance risankizumab. Conclusions Subcutaneous risankizumab maintenance therapy results in durable improvement in clinical and endoscopic outcomes over 1 year in patients with moderately to severely active Crohn’s disease. Clinical trial registration number NCT03105102.

Funder

AbbVie

Publisher

Oxford University Press (OUP)

Subject

Gastroenterology,General Medicine

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