WO2026105071 - ANTI-THYMIC STROMAL LYMPHOPOIETIN (TSLP) MONOCLONAL ANTIBODIES AND METHODS OF TREATING ATOPIC DERMATITIS

National phase entry is expected:
Publication Number WO/2026/105071
Publication Date 21.05.2026
International Application No. PCT/IB2025/061679
International Filing Date 15.11.2025
Title **
[English] ANTI-THYMIC STROMAL LYMPHOPOIETIN (TSLP) MONOCLONAL ANTIBODIES AND METHODS OF TREATING ATOPIC DERMATITIS
[French] ANTICORPS MONOCLONAUX ANTI-LYMPHOPOÏÉTINE STROMALE THYMIQUE (TSLP) ET MÉTHODES DE TRAITEMENT DE LA DERMATITE ATOPIQUE
Applicants **
BIOSION INC.
Inventors
CHEN, Mingjiu
DAVIS, Hugh Michael
Priority Data
63/721,235   15.11.2024   US
63/869,888   25.08.2025   US
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Quotation for National Phase entry

Country StagesTotal
China Filing, Examination, Granting2672
EPO Filing, Examination, Granting12499
Japan Filing, Examination, Granting2327
South Korea Filing, Examination, Granting2393
USA Filing, Examination, Granting4740
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Total: 24,631
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Abstract[English] The present disclosure relates to monoclonal antibodies that specifically bind to thymic stromal lymphopoietin (TSLP) and methods for treating atopic dermatitis. The antibodies block TSLP interaction with its receptor complex, preventing downstream inflammatory signaling. Administration involves weekly loading doses followed by biweekly maintenance doses, achieving superior clinical efficacy with >90% reduction in disease severity. The antibodies demonstrate favorable pharmacokinetics with a 25-day half-life, low immunogenicity, and a well-tolerated safety profile. This disclosure also covers methods for evaluating treatment efficacy and safety in moderate to severe atopic dermatitis patients.[French] La présente divulgation concerne des anticorps monoclonaux qui se lient de manière spécifique à la lymphopoïétine stromale thymique (TSLP) et des méthodes de traitement de la dermatite atopique. L'anticorps bloque l'interaction TSLP avec son complexe récepteur, empêchant une signalisation inflammatoire en aval. L'administration implique le chargement hebdomadaire de doses suivies par des doses d'entretien bihebdomadaire, ce qui permet d'obtenir une efficacité clinique supérieure avec > 90% de réduction de la gravité de la maladie. Les anticorps démontrent une pharmacocinétique favorable avec une demi-vie de 25 jours, une faible immunogénicité et un profil de sécurité bien toléré. La présente divulgation concerne également des procédés d'évaluation de l'efficacité de traitement et de la sécurité chez des patients atteints de dermatite atopique modérée à grave.

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