Implantable device for continuous delivery of interferon
View Patent ↗An implantable device includes a reservoir containing a suspension of an interferon in an amount sufficient to provide continuous delivery of the interferon at a therapeutically effective rate of 1 ng/day to 600 μg/day to maintain and achieve therapeutic blood or plasma levels of the interferon throughout a substantial period of the administration period.
1. An implantable device comprising:
a reservoir containing a suspension formulation comprising
a non-aqueous, single-phase vehicle consisting essentially of about 20% to 60% (w/w) benzyl benzoate and about 40% to 80% (w/w) polyvinylpyrrolidone, the vehicle exhibiting viscous fluid characteristics; and
a particle formulation dispersed in the vehicle, the particle formulation comprising an interferon, a carbohydrate, methionine, and a buffer.
2. The implantable device of claim 1 , wherein the reservoir contains 0.5 to 2.5 mg of the interferon.
3. The implantable device of claim 1 , the device capable of providing continuous delivery of the interferon at a therapeutically effective rate within 1 ug/day to 100 ug/day.
4. The implantable device of claim 1 , the device capable of providing continuous delivery of the interferon at a therapeutically effective rate within 10 ug/day to 50 ug/day.
5. The implantable device of claim 1 , wherein the polyvinylpyrrolidone has a molecular weight of between about 2,000 to about 1,000,000.
6. The implantable device of claim 1 , wherein a concentration of the buffer in the particle formulation is in a range from 5 mM to 50 mM.
7. The implantable device of claim 1 , wherein the interferon is interferon omega.
8. The implantable device of claim 1 , wherein the carbohydrate is sucrose and the buffer is citrate.
9. The implantable device of claim 1 , wherein the vehicle is present in the suspension formulation in an amount greater than 60 wt %.
10. The implantable device of claim 1 , wherein the particle formulation is present in the suspension formulation in a range from 0.01 to 40 wt %.
11. The implantable device of claim 1 , wherein the interferon is present in the particle formulation in an amount ranging from 0.1 to 99.9 wt %.
12. The implantable device of claim 1 , wherein the carbohydrate, methionine, and buffer are each stabilizers and a weight ratio of each stabilizer to the interferon is in a range from 0.1 to 99.9.
13. The implantable device of claim 12 , wherein the carbohydrate, methionine, and buffer are each stabilizers and a weight ratio of each stabilizer to the interferon is greater than 0.5.
14. The implantable device of claim 1 , wherein the interferon is selected from the group consisting of Type I and Type II interferons.
15. The implantable device of claim 1 , wherein the suspension particle formulation comprises 1:2:1:1.5-2.5 interferon:carbohydrate:antioxidant and/or amino acid:buffer.
16. The implantable device of claim 15 , wherein the interferon is interferon omega, the carbohydrate is sucrose, the antioxidant and/or amino acid is methionine, and the buffer is citrate.
17. The implantable device of claim 1 , wherein the particle formulation is spray dried.
18. The implantable device of claim 1 , wherein the particle formulation is lyophilized.
19. The implantable device of claim 1 , further comprising an osmotic pump and a delivery orifice.
20. The implantable device of claim 19 , wherein particles of the particle formulation are sized for delivery through the delivery orifice.
21. The implantable device of claim 20 , wherein the particles have an average particle diameter less than 50 um.
22. The implantable device of claim 20 , wherein the particles have an average particle diameter less than 10 um.
23. The implantable device of claim 20 , wherein the particles have an average particle diameter less than 7 um.
24. A method of treating an interferon-responsive disorder comprising implanting in a subject the device of claim 1 .
25. The method of claim 24 , wherein the disorder is hepatitis C virus disorder.
26. A method of treating an interferon-responsive disorder comprising implanting in a subject the device of claim 16 .
27. The method of claim 26 , wherein the disorder is hepatitis C virus disorder.
28. The implantable device of claim 1 , the device capable of providing continuous delivery of the interferon at a therapeutically effective rate within about 1 ng/day to about 600 ug/day.
29. An implantable device comprising:
a reservoir containing a flowable suspension formulation comprising
a non-aqueous, single-phase vehicle consisting essentially of about 20% to 60% (w/w) benzyl benzoate and about 40% to 80% (w/w) polyvinylpyrrolidone, the vehicle exhibiting viscous fluid characteristics; and
a particle formulation dispersed in the vehicle, the particle formulation comprising an interferon, a carbohydrate, methionine, and a buffer, wherein the device comprises an osmotic pump and is capable of delivering the flowable suspension formulation at a uniform, controlled rate over at least about 1 month.
30. An implantable device comprising:
a reservoir containing a flowable suspension formulation comprising a non-aqueous, single-phase vehicle consisting essentially of about 20% to 60% (w/w) benzyl benzoate and about 40% to 80% (w/w) polyvinylpyrrolidone, the vehicle exhibiting viscous fluid characteristics; and
a particle formulation dispersed in the vehicle, the particle formulation comprising an interferon, a carbohydrate, methionine and a buffer, wherein the particle formulation has a moisture content of about 5% or below by weight.
31. The implantable device of claim 1 , wherein the non-aqueous, single-phase vehicle consists essentially of about 50% (w/w) polyvinylpyrrolidone and about 50% (w/w) benzyl benzoate.
32. The implantable device of claim 1 , wherein the carbohydrate of the particle formulation is selected from the group consisting of monosaccharides, disaccharides, and alditols.
33. The implantable device of claim 1 , wherein the interferon of the particle formulation is selected from the group consisting of interferon alpha, interferon beta, interferon gamma, and interferon omega.