Risperidone-containing implants and methods of use thereof
The present invention provides implants comprising a therapeutic drug and a polymer containing polylactic acid (PLA) and optionally polyglycolic acid (PGA). The present invention also provides methods of maintaining a therapeutic level of a drug in a subject, releasing a therapeutic drug at a substantially linear rate, and treating schizophrenia and other diseases and disorders, utilizing implants of the present invention.
1. A method for treating schizophrenia in a subject in need thereof, the method comprising: administering to said subject a controlled release composition for providing an implant, said composition comprising a therapeutic drug and a polymer, said polymer comprising polylactic acid (PLA) and optionally polyglycolic acid (PGA) in a PLA:PGA molar ratio between 50:50 and 100:0, wherein said therapeutic drug is present in an amount of about 10%-60% of the mass of said composition, wherein the presence of said polymer in said composition extends the release duration of said therapeutic drug in a subject, and wherein said therapeutic drug is risperidone or 9-OH-risperidone, thereby treating said schizophrenia in said subject.
2. The method of claim 1 , wherein said drug is present in an amount of about 40%.
3. The method of claim 1 , wherein said drug is present in an amount of about 30%.
4. The method of claim 1 , wherein said drug is present in an amount of about 20%.
5. The method of claim 1 , wherein said drug is present in an amount of about 10%.
6. The method of claim 1 , wherein said at least one biodegradable polymer is present in an amount of about 20-90%.
7. The method of claim 1 , wherein said polymer is a biodegradable polymer.
8. The method of claim 1 , wherein said polymer is present in an amount of about 20%.
9. The method of claim 1 , wherein said polymer is present in an amount of about 30%.
10. The method of claim 1 , wherein said polymer is present in an amount of about 40%.
11. The method of claim 1 , wherein said composition exhibits an inherent viscosity ranging from about 0.2 dl/g to about 0.9 dl/g.
12. A method for treating schizophrenia in a subject in need thereof, the method comprising: administering to said subject a controlled release composition for providing an implant, said composition comprising a therapeutic drug and a polymer, said polymer comprising polylactic acid (PLA) and optionally polyglycolic acid (PGA), wherein said therapeutic drug is risperidone or 9-OH-risperidone and is present in an amount of about 10%-60% of the mass of said composition, said composition maintaining a therapeutic level of the therapeutic drug over a period ranging from about 1 month to about 6 months upon subcutaneous placement into a subject, thereby treating said schizophrenia in said subject.
13. A method for treating schizophrenia in a subject in need thereof, the method comprising: administering to said subject a biodegradable implant comprising a therapeutic drug and a polymer, said polymer comprising polylactic acid (PLA) and optionally polyglycolic acid (PGA), wherein said therapeutic drug is present in an amount of about 10%-60% of the mass of said implant, said therapeutic drug is risperidone or 9-OH-risperidone, and wherein said implant maintains a therapeutic level of the therapeutic drug over a period ranging from about 1 month to about 6 months and said implant is of a shape suitable for tolerability in the subcutaneous space of a subject, thereby treating said schizophrenia in said subject.
14. A method for treating schizophrenia in a subject in need thereof, the method comprising: subcutaneously providing a controlled release composition into said subject, said composition comprising a therapeutic drug and a polymer, said polymer comprising polylactic acid (PLA) and optionally polyglycolic acid (PGA), wherein said therapeutic drug is present in an amount of about 10%-60% of the mass of said composition, wherein said therapeutic drug comprises risperidone or 9-OH-risperidone, wherein said composition provides a biodegradable implant, and wherein said implant is capable of maintaining a therapeutic level of said drug for a period ranging from about 1 month to about 6 months, thereby treating said schizophrenia in said subject.