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Long-Term Safety and Efficacy of Risankizumab Treatment in Patients with Crohn's Disease: Results from the Phase 2 Open-Label Extension Study.
- Source :
-
Journal of Crohn's & colitis [J Crohns Colitis] 2021 Dec 18; Vol. 15 (12), pp. 2001-2010. - Publication Year :
- 2021
-
Abstract
- Background and Aims: Risankizumab, an interleukin-23 antibody, demonstrated efficacy and acceptable safety in a phase 2 study of patients with moderate-to-severe refractory Crohn's disease. This open-label extension investigated the long-term safety, pharmacokinetics, immunogenicity and efficacy of risankizumab in responders to risankizumab in the parent phase 2 study.<br />Methods: Enrolled patients had achieved clinical response [decrease in Crohn's Disease Activity Index from baseline ≥100] without clinical remission [Crohn's Disease Activity Index <150] at Week 26, or clinical response and/or remission at Week 52 in the parent phase 2 study and received open-label subcutaneous risankizumab 180 mg every 8 weeks.<br />Results: Sixty-five patients were enrolled, including four who had lost response in the parent study and were first reinduced with risankizumab 600 mg every 4 weeks [three infusions]. Patients received risankizumab for a median of 33 months [total: 167.0 patient-years]. The rate of serious adverse events was 24.6 events/100 patient-years; the majority were gastrointestinal in nature. Rates of serious infections, opportunistic infections and fungal infections were 4.2, 1.8, and 6.6 events/100 patient-years, respectively. No deaths, malignancies, adjudicated major adverse cardiovascular events, latent/active tuberculosis or herpes zoster were reported. Treatment-emergent anti-drug antibodies developed in eight patients [12.3%]; none were neutralizing. Efficacy outcomes were maintained during the study, including the proportions of patients [observed analysis] with clinical remission [>71%] and endoscopic remission [>42%].<br />Conclusions: Long-term maintenance treatment with subcutaneous risankizumab 180 mg every 8 weeks was well tolerated by patients with Crohn's disease, with no new safety signals. Clinical trial registration number: NCT02513459.<br /> (© The Author(s) 2021. Published by Oxford University Press on behalf of European Crohn’s and Colitis Organisation.)
- Subjects :
- Adolescent
Adult
Aged
Antibodies, Monoclonal administration & dosage
Antibodies, Monoclonal pharmacokinetics
Female
Gastrointestinal Agents administration & dosage
Gastrointestinal Agents pharmacokinetics
Humans
Injections, Subcutaneous
Male
Middle Aged
Treatment Outcome
Young Adult
Antibodies, Monoclonal therapeutic use
Crohn Disease drug therapy
Gastrointestinal Agents therapeutic use
Opportunistic Infections etiology
Subjects
Details
- Language :
- English
- ISSN :
- 1876-4479
- Volume :
- 15
- Issue :
- 12
- Database :
- MEDLINE
- Journal :
- Journal of Crohn's & colitis
- Publication Type :
- Academic Journal
- Accession number :
- 34077509
- Full Text :
- https://doi.org/10.1093/ecco-jcc/jjab093