IP Library Granted Patent US 9,375,420
Granted Patent B2
US 9,375,420 · App. 14/657,667 · Granted Jun 28, 2016

Methods and compositions for treating infections comprising a local anesthetic

Inventor: Vanja Margareta King (Memphis, TN)
Assignee: Warsaw Orthopedic, Inc.
A61K31/445A61K9/0024A61K9/06A61K9/7007A61K47/34
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Quick Facts
Patent No.
US 9,375,420
App. No.
14/657,667
Granted
Jun 28, 2016
Kind
B2
Abstract

The present invention is directed to a drug depot useful for reducing, preventing or treating an infection in a patient in need of such treatment. The drug depot includes a polymer and a therapeutically effective amount of a local anesthetic or pharmaceutically acceptable salt thereof. The drug depot is administered at a site to reduce, prevent or treat an infection. The drug depot is capable of releasing (i) a bolus dose of the local anesthetic or pharmaceutically acceptable salt thereof at the site and (ii) a sustained release dose of an effective amount of the local anesthetic or pharmaceutically acceptable salt thereof over a period of at least 4 days at the site.

Claims (3)

1. A method of treating or preventing an infection in a patient in need of such treatment, the method comprising administering one or more biodegradable drug depots comprising a polymer and a therapeutically effective amount of a local anesthetic comprising bupivacaine or pharmaceutically acceptable salt thereof, the drug depot being administered at a site to reduce, prevent or treat an infection, wherein the drug depot is capable of releasing (i) a bolus dose of the local anesthetic or pharmaceutically acceptable salt thereof at the site from a layer, wherein between 15 and 25% of the bupivacaine is released within a 24 hour period and (ii) a sustained release dose of an effective amount of the local anesthetic or pharmaceutically acceptable salt thereof over a period of at least 4 days at the site, wherein the polymer comprises a particle size of about 10 μm to about 40 μm and is capable of degrading in less than 30 days after the drug depot is administered at the site.

2. A method of treating or preventing an infection according to claim 1 , wherein the drug depot is capable of releasing between 50 and 800 mg/day of the local anesthetic or pharmaceutically acceptable salt thereof for a period of 4 to 10 days.

3. A method of treating or preventing an infection according to claim 1 , 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.

Continuity (3)
Division 12614711 · Nov 9, 2009
Provisional Application 61140368 · Dec 23, 2008
Related Publication 20150182512A1 · Jul 2, 2015