Long-term efficacy and safety of netakimab in patients with moderate-to-severe psoriasis. Results of phase II open-label extension clinical study BCD-085-2-ext

Author:

Bakulev A. L.1,Samtsov A. V.2,Kubanov A. A.3,Khairutdinov V. R.2,Kokhan M. M.4,Artemyeva A. V.5,Derbin S. I.5,Chernyaeva E. V.5,Ivanov R. A.5

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.

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