High-surface-area lyophilized composition containing arsenic for oral administration to patients
The development of an oral lyophilized arsenic trioxide formulation addresses the limitations of intravenous administration by providing comparable bioavailability and convenience, enhancing solubility and stability for treating hematological malignancies.
Patent Information
- Authority / Receiving Office
- JP · JP
- Patent Type
- Patents
- Current Assignee / Owner
- Filing Date
- 2024-08-14
- Publication Date
- 2026-07-06
AI Technical Summary
Conventional arsenic treatments for hematological malignancies require daily intravenous administration, which is inconvenient, risky, and costly, and there is no FDA-approved oral formulation available.
A lyophilized composition containing arsenic trioxide is developed, which can be administered orally, enhancing bioavailability and solubility through a process involving solubilization and freeze-drying, and optionally incorporating fillers and lubricants.
The oral formulation provides systemic bioavailability comparable to intravenous administration, offers a convenient and less dangerous method, and maintains stability for over three months, with improved solubility and bioavailability.
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