Abstract
In April 2019, the USFDA has approved the humanized monoclonal antibody IgG, Risankizumab, that targets the protein p19 subunit of interleukin (IL-23), for the treatment of moderate to severe plaque psoriasis. The drug was developed by the AbbVie in collaboration with known Boehringer Ingelheim for the management similar immune-mediated inflammatory disorders like inflammatory bowel disease, rheumatic arthritis, etc. The recommended treatment in the case of plague psoriasis with Risankizumab was to begin with 2 initial doses amounts to 150 mg given at baseline (week 0) and again at week 4 that will be followed by 150 mg thereafter by 2 injections every 12 weeks. This article provides a hand on review regarding the drug with all the recent trials and indications.
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References
Boehncke W-H, Schön MP. Psoriasis. Lancet. 2015;386(9997):983–94.
Chiricozzi A, Antonioli L, Panduri S, Fornai M, Romanelli M, Blandizzi C. Risankizumab for the treatment of moderate to severe psoriasis. Expert Opin Biol Ther. 2019;19(1):1–8.
Kaplon H, Reichert JM. Antibodies to watch in 2019. InMAbs. 2019;11(2):219–38.
Menter A, Strober BE, Kaplan DH, Kivelevitch D, Prater EF, Stoff B, et al. Joint AAD-NPF guidelines of care for the management and treatment of psoriasis with biologics. J Am Acad Dermatol. 2019;80(4):1029–72.
Hawkes JE, Chan TC, Krueger JG. Psoriasis pathogenesis and the development of novel targeted immune therapies. J Allergy Clin Immunol. 2017;140(3):645–53.
Fotiadou C, Lazaridou E, Sotiriou E, Ioannides D. Targeting IL-23 in psoriasis: current perspectives. Psoriasis (Auckl). 2018;8:1–5.
Machado Á, Torres T. Spotlight on risankizumab and its potential in the treatment of plaque psoriasis: evidence to date. Psoriasis (Auckl). 2018;8:83–92.
Krueger JG, Ferris LK, Menter A, Wagner F, White A, Visvanathan S, et al. Anti-IL-23A mAb BI 655066 for treatment of moderate-to-severe psoriasis: safety, efficacy, pharmacokinetics, and biomarker results of a single-rising-dose, randomized, double-blind, placebo-controlled trial. J Allergy Clin Immunol. 2015;136(1):116–24.
Gordon KB, Strober B, Lebwohl M, Augustin M, Blauvelt A, Poulin Y, et al. Efficacy and safety of risankizumab in moderate-to-severe plaque psoriasis (UltIMMa-1 and UltIMMa-2): results from two double-blind, randomised, placebo-controlled and ustekinumab-controlled phase 3 trials. Lancet. 2018;392(10148):650–61.
Khatri A, Cheng L, Camez A, Ignatenko S, Pang Y, Othman AA. Lack of effect of 12-week treatment with risankizumab on the pharmacokinetics of cytochrome P450 probe substrates in patients with moderate to severe chronic plaque psoriasis. Clin Pharmacokinet. 2019;58(6):805–14.
Drugs and Lactation Database (LactMed) [Internet]. Bethesda (MD): National Library of Medicine (US);2006. Risankizumab.[Updated 2019 May 1].
Ohtsuki M, Fujita H, Watanabe M, Suzaki K, Flack M, Huang X, et al. Efficacy and safety of risankizumab in Japanese patients with moderate to severe plaque psoriasis: results from the SustaIMM phase 2/3 trial. J Dermatol. 2019;46(8):686–94.
Zhang TT, Ma J, Durbin KR, Montavon T, Lacy SE, Jenkins GJ, et al. Determination of IL-23 pharmacokinetics by highly sensitive accelerator mass spectrometry and subsequent modeling to project IL-23 suppression in psoriasis patients treated with anti-IL-23 antibodies. AAPS J. 2019;21(5):82.
Feldman SR, Krueger GG. Psoriasis assessment tools in clinical trials. Ann Rheum Dis. 2005;64:ii 65–8.
Papp KA, Blauvelt A, Bukhalo M, Gooderham M, Krueger JG, Lacour JP, et al. Risankizumab versus ustekinumab for moderate-to-severe plaque psoriasis. N Engl J Med. 2017;376(16):1551–60.
Blauvelt A, Papp KA, Gooderham M, Langley RG, Leonardi C, Lacour JP, et al. Risankizumab efficacy/safety in moderate-to-severe plaque psoriasis: 16-week results from immhance. Acta Dermatol Venereol. 2018;98(Supplement 219):30. https://doi.org/10.2340/00015555-2978.
McKeage K, Duggan S. Risankizumab: first global approval. Drugs. 2019;79(8):893–900.
Suleiman AA, Minocha M, Khatri A, Pang Y, Othman AA. Population pharmacokinetics of Risankizumab in healthy volunteers and subjects with moderate to severe plaque psoriasis: integrated analyses of phase I-III clinical trials. Clin Pharmacokinet. 2019;58(10):1309–21.
Khatri A, Eckert D, Oberoi R, Suleiman A, Pang Y, Cheng L, et al. Pharmacokinetics of Risankizumab in Asian healthy subjects and patients with moderate to severe plaque psoriasis, generalized pustular psoriasis, and erythrodermic psoriasis. J Clin Pharmacol. 2019;59(12):1656–68.
Puig L. The role of IL 23 in the treatment of psoriasis. Expert Rev Clin Immunol. 2017;13(6):525–34.
Crowley JJ, Warren RB, Cather JC. Safety of selective IL-23p19 inhibitors for the treatment of psoriasis. J Eur Acad Dermatol Venereol. 2019;33(9):1676–84.
Gaspari AA, Tyring S. New and emerging biologic therapies for moderate-to-severe plaque psoriasis: mechanistic rationales and recent clinical data for IL-17 and IL-23 inhibitors. Dermatol Ther. 2015;28(4):179–93.
Reich K, Gooderham M, Thaçi D, Crowley JJ, Ryan C, Krueger JG, et al. Risankizumab compared with adalimumab in patients with moderate-to-severe plaque psoriasis (IMMvent): a randomised, double-blind, active-comparator-controlled phase 3 trial. Lancet. 2019;394(10198):576–86.
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Varthya, S.B., Thangaraju, P., Venkatesan, S. et al. A Nonsystematic Review on Risankizumab: a Novel Drug Recently Approved for Moderate to Severe Psoriasis. SN Compr. Clin. Med. 2, 1174–1180 (2020). https://doi.org/10.1007/s42399-020-00356-3
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DOI: https://doi.org/10.1007/s42399-020-00356-3