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Volume 4, Issue 3 (Suppl) J Pigment Disord
ISSN: 2376-0427 JPD, an open access journal Dermatology Conference 2017
October 26-28, 2017
Page 14
conferenceseries.com
October 26-28, 2017 Osaka, Japan
23rd Asia-Pacific
Dermatology Conference
Anti-IL-17 nanobody: A future option in treatment of psoriasis
An improved understanding of the pathogenesis of psoriasis has led to the development of multiple new potential targets for
therapy. The first pathway targeted by new biologics focus on the p40 subunit that is shared by interleukin (IL)-12 and IL-
23. Second new strategy focuses IL-17 or its receptor. Secukinumab is fully human monoclonal G1 antibody targeting IL-17A,
approved in EU for the first-line systemic therapy of moderate-to-severe plaque psoriasis. New IL-17 inhibitors, Ixekizumab and
Brodalumab achieved very good efficacy and are currently in administration approved review. We demonstrate the preliminary
results of the anti-IL-17 A/F bispecific nanobody that neutralize the pro-inflammatory cytokines IL-17A and IL-17F. We
present results of multicentric, phase I, randomized, double -blind, placebo controlled study investigated multiple ascending
doses of anti-IL-17 A/F nanobody (M1095) in patients with moderate-to-severe psoriasis. Body surface area (BSA) ≥10%,
Psoriasis Area and Severity Index (PASI) ≥12 and static Physician’s Global Assessment (sPGA) ≥3 were evaluated. Patients
received 30, 60, 120 or 240 mg anti-IL-17 A/F nanobody or placebo every two weeks subcutaneously for 6 weeks. Primary
endpoints were safety, tolerability, immunogenicity and pharmacokinetics. Secondary endpoints were pharmacodynamics,
efficacy and histological analysis. On day 85, 6 weeks after the last dose of the drug, PASI 75 was achieved in 7/8 patients (88%)
receiving 30 or 60 mg, 8/8 (100%) receiving 120 mg and 9/9 (100%) receiving 240 mg of drug. PASI 90 was achieved in 4/8
(50%), 7/8 (88%) and 9/9 (100%) patients receiving 30 mg, 60 mg, 120 mg or 240 mg, respectively. PASI 100 was achieved in
1/8 (13%), 2/8 (25%), 4/8 (50%) and 5/9 (56%) patients receiving 30 mg, 60 mg, 120 mg or 240 mg, respectively. Improved PASI
scores were seen 7 days post-first dose in all 4 cohorts. Biopsy assessment of skin lesion showed complete reversal of disease
pathology in majority of patients in high dose groups. Conclusion can be drawn that Anti-IL-17 A/F bispecific nanobody
presents a new treatment option well tolerated and effective in patients with moderate-to-severe psoriasis associated with skin
clearance improvement in all indices of psoriasis studied.
Biography
Danka Svecova is presently a Professor of Dermatovenerology, Head of Bullous Disorders Unit, Department of Dermatovenerology, University Hospital and Faculty
of Medicine, Comenius University, Slovakia. She is a Board Member of Committee for Dermatovenerology and Immunology dissertation for PhD at Comenius
University and a Member of Committee for Probation of Specialization for Dermatovenerology at Comenius University and University of JP Safarik in Kosice. She
has participated in research on Skin Allergology and Immunology under the supervision of Professor Akira Ohkawara at Hokkaido University in Sapporo, Japan.
She wrote two monographs about blistering disorders-Pemphigus vulgaris autoimmune disease and Pemphigus.
Danka Svecova
Comenius University, Slovakia
Danka Svecova, J Pigment Disord 2017, 4:3(Suppl)
DOI: 10.4172/2376-0427-C1-004