Claims for Patent: 10,350,171
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Summary for Patent: 10,350,171
| Title: | Celecoxib and amlodipine formulation and method of making the same |
| Abstract: | Provided herein is a celecoxib and amlodipine composition and method of making the same. The composition contains granules containing celecoxib. The amlodipine is incorporated into the composition as an extragranulate. |
| Inventor(s): | Efrati; Yitshak Itsik (Modiin, IL) |
| Assignee: | Dexcel Ltd. (Or-Akiva, IL) Kitov Pharmaceuticals (Tel Aviv, IL) |
| Application Number: | 16/008,538 |
| Patent Litigation and PTAB cases: | See patent lawsuits and PTAB cases for patent 10,350,171 |
| Patent Claims: |
1. A method of preparing a pharmaceutical composition comprising celecoxib and amlodipine or pharmaceutically acceptable salts thereof, the method comprising the steps
of: (i) wet granulating celecoxib or a pharmaceutically acceptable salt thereof and one or more excipients to obtain a wet granulate, wherein said wet granulate does not include amlodipine; (ii) drying the wet granulate of step (i) to obtain a dry
granulate having a loss on drying (LOD) % of about 2.5% or less; and (iii) admixing the dry granulate of step (ii) with an extragranulate comprising amlodipine or a pharmaceutically acceptable salt thereof and optionally one or more excipients.
2. The method of claim 1, wherein the dry granulate has LOD % in the range of from about 0.5% to about 2%. 3. The method of claim 2, wherein the dry granulate has LOD % in the range of from about 0.5% to about 1.5%. 4. The method of claim 1, wherein step (i) comprises dry mixing celecoxib or a pharmaceutically acceptable salt thereof and one or more excipients to obtain a dry mixture, and spraying the dry mixture with a granulation solution or suspension to obtain a wet granulate. 5. The method of claim 4, wherein the granulation solution or suspension comprises an aqueous medium. 6. The method of claim 4, wherein the granulation solution or suspension comprises an organic medium. 7. The method of claim 1, wherein the extragranulate in step (iii) comprises one or more excipients, and wherein the one or more excipients in the wet granulate of step (i) and the one or more excipients in the extragranulate of step (iii) are the same or different selected from the group consisting of a diluent, a disintegrant, a surfactant, a binder, a glidant, a lubricant, and combinations thereof. 8. The method of claim 1 further comprising a step of milling the dry granulate of step (ii) to produce a milled dry granulate prior to step (iii). 9. The method of claim 1, further comprising a step of compressing the phamiaceutical composition to obtain a tablet or a caplet. 10. A pharmaceutical composition prepared by the method of claim 1. |
