Affiliation:
1. Saratov State Medical Universit y named after V. I. Razumovsky, Ministr y of Health of the Russian Federation
2. S. M. Kirov Militar y Medical Academy, Ministr y of Defence of the Russian Federation
3. State Research Center of Dermatovenereology and Cosmetology, Ministr y of Health of the Russian Federation
4. Ural Research Institute for Dermatovenerology and Immunopatology
5. BIOCAD
Abstract
Netakimabis original monoclonal antibody against IL-17. This article outlines the key results of a phase II open-label extension trial of netakimab 80 mg and 120 mg in patients with moderate-to-severe psoriasis.The main aim of the trial is to estimate efficacy, safety and immunogenicity of long-term treatment with netakimab 80 mg and 120 mg in patients with moderate-to-severe psoriasis.Materials and methods. The BCD-085-2-ext study is a comparative, open-label phase 2 clinical study of the effi - cacy and safety of netakimab in patients with moderate-to-severe plaque psoriasis who had finished BCD-085-2 (NCT02762994) trial. Main efficacy endpoints includePASI75, PASI90, PASI100, sPGA = 0–1 on week 38 of the trial, long-term PASI75/90/100 retention, efficacy keeping after switch from once every 2 week regimen to once every 4 week regimen. Safety endpoints include adverse events, serious adverse events number and their profile.Results. 103 patients were included. PASI75 at week 38 was reached by 98.06 %, PASI90 — by 92.23 %, PASI100 — by 59.22 % of patients. There were no cases of serious adverse event, early with drawal due to adverse events and cases of grade 4 toxicity according to CTCAE 4.03. There were no cases of binding antibodies to netakimab during the 38 weeks of the study.Conclusion. The first Russian original IL-17 inhibitor netakimabis promising modern medicine for moderate-to-severe plaque psoriasis treatment. Netakimabshowed high efficacy, favorable safety profile and low immunogenicity during one year of the treatment.
Publisher
Rossijskoe Obschestvo Dermatovenerologov i Kosmetologov
Reference18 articles.
1. Кубанова А. А., Кубанов А. А., Знаменская Л. Ф., Чикин В.В., Бакулев А. Л., Хобейш М. М. и др. Псориаз. В кн.: Федеральные клинические рекомендации. Дерматовенерология, 2015: Болезни кожи. Инфекции, передаваемые половым путем. 5-е изд., перераб. и доп. М.: Деловой экспресс, 2016. С. 415–470. [Kubanova A. A., Kubanov A. A., Znamenskaya L. F., Chikin V. V., Bakulev A. L., Khobeysh M. M. et al. Psoriasis. In: Federal clinical guidelines. Dermatovenerology, 2015: Diseases of the skin. Sexually transmitted infections. 5th ed., revised and enlarged. Moscow: Delovoy ekspress, 2016. P. 415–470. (In Russ.)]
2. Бакулев А. Л. Эволюция представлений о псориазе и терапевтических подходах по ведению пациентов. BCD-085 — первый отечественный генно-инженерный биологический препарат для лечения больных псориазом. Вестник дерматологии и венерологии. 2018;94(5):26–32. [Bakulev A. L. Evolution of the understanding of psoriasis and therapeutic approaches used to managesuch patients. BCD-085 is the first Russian genetically- engineered biological preparation for the treatment of patients suffering from psoriasis. Vestnik Dermatologii i Venerologii. 2018;94(5):26–32. (In Russ.)]. DOI: 10.25208/0042-4609-2018-94-5-26-32
3. Bovenschen H. J., Van de Kerkhof P. C., Van Erp P. E. et al. Foxp3+ Regulatory T Cells of Psoriasis Patients Easily Differentiate into IL-17A-Producing Cells and Are Found in Lesional Skin. Journal of Investigative Dermatology. 2011;131:1853–1860.
4. Cua Daniel J., Tato Cristina M. Innate IL-17-producing cells: the sentinels of the immune system. Nature Reviews Immunology. 2010/06/18/online. DOI: 10.1038/nri2800
5. Korn T., Bettelli E., Oukka M., Kuchroo V. K. IL-17 and Th17 Cells. Annu Rev Immunol. 2009;27:485–517.
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