التفاصيل البيبلوغرافية
| العنوان: |
Efficacy and safety of risankizumab for active psoriatic arthritis: 52-week results from the KEEPsAKE 2 study. |
| المؤلفون: |
Östör, Andrew, Bosch, Filip Van den, Papp, Kim, Asnal, Cecilia, Blanco, Ricardo, Aelion, Jacob, Lu, Wenjing, Wang, Zailong, Soliman, Ahmed M, Eldred, Ann, Padilla, Byron, Kivitz, Alan |
| المصدر: |
Rheumatology; Jun2023, Vol. 62 Issue 6, p2122-2129, 8p |
| مصطلحات موضوعية: |
BIOTHERAPY, THERAPEUTIC use of monoclonal antibodies, PSORIATIC arthritis, INTERLEUKINS, DRUG efficacy, PSORIASIS, TREATMENT effectiveness, PLACEBOS, RANDOMIZED controlled trials, STATISTICAL sampling, PATIENT safety, LONGITUDINAL method, CHEMICAL inhibitors |
| مستخلص: |
Objective PsA is a chronic inflammatory disease in which the skin and joints are affected. In this follow-up analysis, the 52-week efficacy and safety of risankizumab 150 mg in patients with active PsA who had previous inadequate response/intolerance to one or two biologic therapies (Bio-IR) or one or more conventional synthetic DMARDs (csDMARD-IR) were evaluated. Methods In the ongoing, phase 3, KEEPsAKE 2 trial, patients with active PsA were randomized 1:1 to receive subcutaneous risankizumab 150 mg or placebo at weeks 0, 4 and 16 (period 1). At week 24 (period 2), patients who received placebo were switched to risankizumab, and all patients received risankizumab 150 mg every 12 weeks from weeks 28 to 208. Results At week 24, 51.3% of risankizumab-treated patients (n = 224) achieved ≥20% improvement in ACR criteria (ACR 20) vs 26.5% of placebo-treated patients (n = 220; P < 0.001). At week 52, 58.5% of patients randomized to receive continuous risankizumab achieved ACR20, and 55.7% of patients who switched from placebo to risankizumab at week 24 achieved ACR20. Similar trends were observed for other efficacy measures. Rates of serious treatment-emergent adverse events (TEAEs) and TEAEs leading to discontinuation remained stable through week 52, and no deaths were reported. Conclusion Risankizumab was well tolerated and improved symptoms of PsA in Bio-IR/csDMARD-IR patients, with a consistent long-term safety profile from weeks 24 to 52. Trial registration United States National Library of Medicine clinical trials database www.clinicaltrials.gov ; KEEPsAKE 2; NCT03671148. [ABSTRACT FROM AUTHOR] |
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| قاعدة البيانات: |
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