Methods and compositions for treating post-operative pain comprising clonidine
The present invention is directed to an implantable drug depot useful for reducing, preventing or treating post-operative pain in a patient in need of such treatment, the implantable drug depot comprising a therapeutically effective amount of clonidine or pharmaceutically acceptable salt thereof and a polymer; wherein the depot is implantable at a site beneath the skin to reduce, prevent or treat post-operative pain, and the depot is capable of releasing (i) about 5% to about 45% of the clonidine or pharmaceutically acceptable salt thereof relative to a total amount of the clonidine or pharmaceutically acceptable salt thereof loaded in the drug depot over a first period of up to 48 hours and (ii) about 55% to about 95% of the clonidine or pharmaceutically acceptable salt thereof relative to a total amount of the clonidine or pharmaceutically acceptable salt thereof loaded in the drug depot over a subsequent period of at least 3 days.
1. An implantable drug depot useful for reducing or treating post-operative pain in a patient in need of such treatment, the implantable drug depot comprising a therapeutically effective amount of clonidine or pharmaceutically acceptable salt thereof in an amount of from about 1% to about 10% by weight based on the total weight of the depot and a polymer; wherein the depot is implantable at a site beneath the skin to reduce or treat post-operative pain, and the depot has an initial burst surface and releases (i) about 5% to about 45% of the clonidine or pharmaceutically acceptable salt thereof relative to a total amount of the clonidine or pharmaceutically acceptable salt thereof loaded in the drug depot over a first period of up to 48 hours, and (ii) about 55% to about 95% of the clonidine or pharmaceutically acceptable salt thereof relative to a total amount of the clonidine or pharmaceutically acceptable salt thereof loaded in the drug depot over a subsequent period of at least 3 days, wherein the polymer comprises poly(D,L-lactide-co-caprolactone) or poly(L-lactide-co-caprolactone) or a combination thereof and the polymer has an inherent viscosity of from about 0.45 dL/g to about 1.00 dL/g.
2. An implantable drug depot according to claim 1 , wherein the clonidine is in the form of a hydrochloric salt.
3. An implantable drug depot according to claim 1 , wherein the polymer comprises about 60% to about 90% of the total wt. % of the drug depot.
4. An implantable drug depot according to claim 1 , wherein the polymer is capable of degrading in 30 days or less after the drug depot is implanted at the site.
5. An implantable drug depot according to claim 1 , wherein the clonidine is released in an amount between 0.05 ug and 3 mg per day for a period of 3 to 10 days.
6. An implantable drug depot according to claim 1 , wherein the clonidine is present in an amount of about 5 wt. % to about 10 wt. % of the implantable drug depot and the polymer is present in an amount of about 75 to about 94 wt. % of the implantable drug depot, and the drug depot further comprises from about 5 to about 15 wt. % of an excipient.
7. An implantable drug depot according to claim 1 , wherein the depot further comprises from about 5 to about 15 wt. % mPEG.
8. A method of making an implantable drug depot of claim 1 , the method comprising combining the polymer and the clonidine or pharmaceutically acceptable salt thereof and forming the implantable drug depot from the combination.
9. A method of treating or preventing post-operative pain in a patient in need of such treatment, the method comprising delivering one or more biodegradable drug depots of claim 1 comprising a therapeutically effective amount of clonidine or pharmaceutically acceptable salt thereof to a target tissue site beneath the skin before, during or after surgery, wherein the drug depot is capable of releasing an initial bolus dose of the clonidine or pharmaceutically acceptable salt thereof at a site beneath the skin followed by a sustained release dose of an effective amount of the clonidine or pharmaceutically acceptable salt thereof over a period of at least 3 days.
10. A method of treating or preventing post-operative pain according to claim 9 , wherein the drug depot releases about 55% to about 85% of the clonidine or pharmaceutically acceptable salt thereof relative to a total amount of the clonidine loaded in the drug depot over a period of 3 to 10 days after the drug depot is administered to the target tissue site.
11. A method of treating or preventing post-operative pain according to claim 9 , wherein the drug depot releases between 0.05 ug and 3 mg/day of the clonidine or pharmaceutically acceptable salt thereof for a period of 4 to 10 days.
12. A method of treating or preventing post-operative pain according to claim 9 , wherein the drug depot comprises a polymer comprising one or more of poly(lactide-co-glycolide), polylactide, polyglycolide, polyorthoester, D-lactide, D,L-lactide, poly(D,L-lactide), L-lactide, poly(D,L-lactide-co-caprolactone), poly(D,L-lactide-co-glycolide-co-caprolactone), polycaprolactone or a combination thereof.
13. A method of treating or preventing post-operative pain according to claim 12 , wherein the polymer comprises about 60% to about 90% of the total wt. % of the drug depot.
14. An implantable drug depot comprising: (i) a therapeutically effective amount of clonidine or pharmaceutically acceptable salt thereof in the depot in an amount of from about 1% to about 10% by weight based on the total weight of the depot; and (ii) a polymer; wherein the drug depot releases an initial bolus dose of clonidine or pharmaceutically acceptable salt thereof at a site beneath the skin, and the drug depot releases a sustained release dose of an effective amount of clonidine or pharmaceutically acceptable salt thereof over a subsequent period of 3 to 10 days; and wherein the polymer comprises poly(D,L-lactide-co-caprolactone), or poly(L-lactide-co-caprolactone) or a combination thereof, wherein the initial bolus dose of the clonidine is about 15% to about 45% of the clonidine or pharmaceutically acceptable salt thereof relative to a total amount of clonidine loaded in the drug depot in 24 hours and the clonidine has a particle size of 1 micrometer to about 200 micrometers and the polymer has an inherent viscosity of from about 0.45 dL/g to about 0.6 dL/g.
15. An implantable drug depot according to claim 14 , wherein the drug depot releases about 55% to about 85% of the clonidine or pharmaceutically acceptable salt thereof relative to a total amount of clonidine loaded in the drug depot over the subsequent period of 3 to 10 days after the drug depot is administered.
16. An implantable drug depot according to claim 14 wherein the drug depot releases between 0.05 ug and 3 mg/day of clonidine or pharmaceutically acceptable salt thereof.
17. An implantable drug depot according to claim 14 , wherein the polymer comprises about 60% to about 90% of the total wt. % of the drug depot.
18. An implantable drug depot according to claim 14 , wherein the clonidine is in the form of a hydrochloric salt.
19. An implantable drug depot according to claim 14 , wherein the initial bolus dose of the clonidine is about 15% relative to a total amount of clonidine loaded in the drug depot.
20. An implantable drug depot according to claim 1 , wherein the drug depot releases 30 mcg to 50 mcg per day of clonidine or pharmaceutically acceptable salt thereof for at least 3 days.
21. An implantable drug depot according to claim 1 , wherein the drug depot has a length of from about 0.5 mm to 100 mm and a thickness of from about 0.01 mm to about 5 mm.
22. An implantable drug depot according to claim 21 , wherein the clonidine has a particle size of 1 micrometer to about 20 micrometers.
23. An implantable drug depot according to claim 21 , wherein the molar ratio of lactide to caprolactone is 10:90.
24. An implantable drug depot according to claim 21 , wherein the molar ratio of lactide to caprolactone is between from 45:55 to 65:35.
25. An implantable drug depot according to claim 23 , wherein the polymer has an average molecular weight of about 10,000 to about 100,000.
26. An implantable drug depot according to claim 24 , wherein the polymer has an average molecular weight of about 20,000 to about 50,000.
27. An implantable drug depot according to claim 21 , wherein the initial burst surface releases from about 5% to about 15% of the clonidine or pharmaceutically acceptable salt thereof relative to a total amount of clonidine loaded in the drug depot.
28. An implantable drug depot according to claim 1 , wherein the polymer has an inherent viscosity of about 0.45 dL/g to about 0.6 dL/g and comprises poly(L-lactide-co-caprolactone).
29. An implantable drug depot according to claim 1 , wherein the polymer has an inherent viscosity of about 0.45 dL/g and comprises poly(L-lactide-co-caprolactone).
30. An implantable drug depot according to claim 1 , wherein the initial burst surface releases about 15% to about 45% of the clonidine or pharmaceutically acceptable salt thereof relative to a total amount of clonidine loaded in the drug depot in 24 hours and the polymer has an inherent viscosity of about 0.45 dL/g and comprises poly(L-lactide-co-caprolactone).