(9R,13S)-13-{4-[5-chloro-2-(4-chloro-1H-1,2,3-triazole-1-yl)phenyl]-6-oxo-1,6-dihydropyrimidine-1-yl}-3-(difluoromethyl)-9-methyl-3,4,7,15-tetraazatricyclo[12.3.1.02,6]octadeca-1(18),2(6),4,14,16-pentaen-8-one crystal
Patent Information
- Authority / Receiving Office
- JP · JP
- Patent Type
- Applications
- Current Assignee / Owner
- BRISTOL MYERS SQUIBB CO
- Filing Date
- 2025-12-17
- Publication Date
- 2026-06-16
AI Technical Summary
Existing pharmaceutical formulations of Compound (I) lack a balance of desirable properties such as dissolution rate, solubility, and bioavailability, making them unpredictable and challenging to manufacture and store, and there is a need for specific polymorphic crystalline forms to address these issues.
The development of crystalline forms A, B, C, D, E, F, G, H, and J of Compound (I), characterized by unique PXRD, IR, DSC, and TGA patterns, which provide a balance of stability, solubility, and bioavailability, suitable for oral administration.
These crystalline forms enhance the stability, solubility, and bioavailability of Compound (I), ensuring consistent and effective pharmaceutical compositions for treating thromboembolic disorders.
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