Oral solid pharmaceutical composition, preparation method therefor, and use thereof

By optimizing the formulation and process of onradivir, especially by using internal and external addition of fillers, the disintegration and dissolution problems of onradivir have been solved, achieving high bioavailability and stable formulation effects, making it suitable for the treatment of influenza A.

WO2026119226A1PCT designated stage Publication Date: 2026-06-11GUANGDONG RAYNOVENT BIOTECH CO LTD

Patent Information

Authority / Receiving Office
WO · WO
Patent Type
Applications
Current Assignee / Owner
GUANGDONG RAYNOVENT BIOTECH CO LTD
Filing Date
2025-12-04
Publication Date
2026-06-11

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  • Figure PCTCN2025139932-FTAPPB-I100001
    Figure PCTCN2025139932-FTAPPB-I100001
  • Figure PCTCN2025139932-FTAPPB-I100002
    Figure PCTCN2025139932-FTAPPB-I100002
  • Figure PCTCN2025139932-FTAPPB-I100003
    Figure PCTCN2025139932-FTAPPB-I100003
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Abstract

The present invention provides an oral solid pharmaceutical composition, comprising onradivir as an active ingredient, an alkaline reagent, and a solubilizer, and further comprising a filler. The oral solid pharmaceutical composition of the present invention effectively improves the solubility of onradivir, improves the bioavailability of onradivir in the human body, and can solve formulation issues, such as the issue where effective disintegration cannot be achieved by means of conventional formulas and processes, which is conducive to achieving the clinical application of onradivir.
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