WO2023203549 - METHODS OF ACHIEVING SAFE AND SUSTAINED CONTROL OF IL-17-DEPENDENT CONDITIONS IN SUBJECTS RESPONSIVE TO TREATMENT WITH AN ANTI-IL 17A/F NANOBODY

National phase entry:
Publication Number WO/2023/203549
Publication Date 26.10.2023
International Application No. PCT/IB2023/054122
International Filing Date 21.04.2023
Title **
[English] METHODS OF ACHIEVING SAFE AND SUSTAINED CONTROL OF IL-17-DEPENDENT CONDITIONS IN SUBJECTS RESPONSIVE TO TREATMENT WITH AN ANTI-IL 17A/F NANOBODY
[French] PROCÉDÉS D'OBTENTION D'UNE COMMANDE SÛRE ET PROLONGÉE D'ÉTATS DÉPENDANTS DE L'IL-17 CHEZ DES SUJETS SENSIBLES À UN TRAITEMENT AVEC UN NANOCORPS ANTI-IL17A/F
Applicants **
MOONLAKE IMMUNOTHERAPEUTICS AG
Inventors
REICH, Kristian
Priority Data
63/333,920   22.04.2022   US
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Quotation for National Phase entry

Country StagesTotal
China Filing, Examination, Granting2890
EPO Filing, Examination, Granting21544
Japan Filing, Examination, Granting2962
South Korea Filing, Examination, Granting3576
USA Filing, Examination, Granting9340
MasterCard Visa
Total: 40,312

The term for entry into the National Phase has expired. This quotation is for informational purposes only

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Abstract[English] Disclosed herein are methods of treating psoriasis and other IL-17-dependent conditions with an anti-interleukin 17A/F nanobody for approximately 24 weeks, followed by withdrawal of treatment in responding patients with the anti-interleukin 17A/F nanobody for a period of at least 4-20 weeks. Disease modification may be achieved by no later than week 24 with the anti- interleukin 17A/F nanobody such that responders may demonstrate sustained normalization of peripheral and/or cutaneous biomarkers such as IL-17A, IL-17F, and/or IL-22. Treatment methods as contemplated herein which have been paused may be re-started based on the subject's condition. Treatment beyond 24 weeks also achieves unexpectedly high efficacy in responders who have not quite reached full skin clearance in the initial treatment period.[French] L'invention concerne des procédés de traitement du psoriasis et d'autres affections dépendantes de l'IL-17 avec un nanocorps anti-interleukine 17A/F pendant environ 24 semaines, suivis de l'arrêt du traitement chez des patients répondant au nanocorps anti-interleukine 17A/F pendant une période d'au moins 4 à 20 semaines. Une modification de maladie peut être obtenue par pas plus tard que la semaine 24 avec le nanocorps anti-interleukine 17A/F de telle sorte que les répondeurs peuvent démontrer une normalisation prolongée de biomarqueurs périphériques et/ou cutanés tels que l'IL-17A, l'IL-17 F, et/ou l'IL-22. Les procédés de traitement selon la présente invention qui ont été mis en pause peuvent être redémarrés sur la base de l'état du sujet. Le traitement au-delà de 24 semaines atteint également une efficacité étonnamment élevée chez des répondeurs qui n'ont pas atteint de clairance de peau complète dans la période de traitement initiale.

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