Dry powder formulations of thymic stromal lymphopoietin (TSLP)-binding antibody and use methods thereof

The combination of leucine and trileucine in the dry powder formulation solved the problem of lung delivery of anti-TSLP antibodies, enabling effective treatment of asthma patients in primary care settings, reducing adverse reactions, and improving compliance.

JP2025169423APending Publication Date: 2025-11-12MEDIMMUNE LTD
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Patent Information

Application Number
JP2025140274
Authority / Receiving Office
JP · JP
Patent Type
Applications
Current Assignee / Owner
Priority Date
2019-10-28
Filing Date
2025-08-26
Publication Date
2025-11-12

AI Technical Summary

Technical Problem

Existing technologies make it difficult to deliver anti-TSLP antibodies to asthma patients via an effective pulmonary route, especially those managed in primary care settings, and systemic administration may lead to adverse reactions.

Method used

Develop a dry powder formulation comprising an anti-TSLP antibody-binding fragment in particulate form, leucine, and trileucine, suitable for pulmonary delivery via a dry powder inhaler.

Benefits of technology

It enables efficient delivery of anti-TSLP antibodies in primary care settings, reduces adverse reactions to systemic administration, improves patient compliance, and increases treatment coverage for asthma patients.

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Abstract

To provide dry powder formulations of antigen-binding fragments derived from a thymic stromal lymphopoietin-specific antibody.SOLUTION: Disclosed is a dry powder formulation comprising a plurality of microparticles, where the microparticles comprise: a. 8-11 wt.% of leucine; b. 2-4 wt.% of trileucine; and c. an antigen-binding fragment of an anti-thymic stromal lymphopoietin antibody.SELECTED DRAWING: None
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