Method for delivering pramlintide into a lumen of the intestinal tract using a swallowable drug delivery device
View Patent ↗Embodiments of the invention provide swallowable devices, preparations and methods for delivering drugs and other therapeutic agents within the GI tract. Many embodiments provide a swallowable device for delivering the agents. Particular embodiments provide a swallowable device such as a capsule for delivering drugs into the intestinal wall or other GI lumen. Embodiments also provide various drug preparations that are configured to be contained within the capsule, advanced from the capsule into the intestinal wall and degrade to release the drug into the bloodstream to produce a therapeutic effect. The preparation can be operably coupled to delivery means having a first configuration where the preparation is contained in the capsule and a second configuration where the preparation is advanced out of the capsule into the intestinal wall. Embodiments of the invention are particularly useful for the delivery of drugs which are poorly absorbed, tolerated and/or degraded within the GI tract.
1. A method for delivering Pramlintide into a wall of an intestine, the method comprising:
providing a swallowable drug delivery device comprising a shell, an actuator having a first configuration and a second configuration and a solid Pramlintide preparation operably coupled to the actuator, the Pramlintide preparation shaped for penetration into the intestine and comprising a therapeutically effective dose of Pramlintide, the preparation being contained within the shell in the first configuration and advanced out of the shell and into the intestinal wall in the second configuration to deliver the Pramlintide preparation into the intestinal wall; and
actuating the actuator within the intestine responsive to a condition in the intestine to deliver the Pramlintide preparation into the wall of the intestine.
2. The method of claim 1 , wherein the condition is a selected pH.
3. The method of claim 2 , wherein the pH is above about 7.1.
4. The method of claim 1 , wherein the intestine is the small intestine.
5. The method of claim 1 , wherein a weight per cent of Pramlintide in the Pramlintide preparation comprises between about 3 to 6 %.
6. The method of claim 1 , wherein a dose of Pramlintide in the Pramlintide preparation is in a range from about 0.1 to 1 mg.
7. The method of claim 6 , wherein the dose of Pramlintide is about 0.6 mg.
8. The method of claim 1 , wherein the Pramlintide preparation comprises at least one pharmaceutical excipient.
9. The method of claim 8 , wherein the at least one pharmaceutical excipient comprises at least one of a binder, a preservative or a disintegrant.
10. The method of claim 9 , wherein the binder comprises PEG.
11. The method of claim 1 , further comprising retaining the Pramlintide preparation within the intestinal wall after insertion.
12. The method of claim 11 , wherein retaining comprises anchoring at least one of a barb or an inverse taper shape of the Pramlintide preparation in the intestinal tissue.
13. The method of claim 1 , wherein delivering the Pramlintide preparation comprises applying a force to the Pramlintide preparation.
14. The method of claim 13 , wherein the Pramlintide preparation is advanced completely into the intestinal wall by such application of force.
15. The method of claim 1 , wherein the Pramlintide preparation produces a long-term release of Pramlintide.
16. The method of claim 1 , further comprising:
using the dose of delivered Pramlintide to control a blood glucose level of a patient.
17. The method of claim 1 , wherein the Pramlintide preparation comprises a therapeutically effective dose of another therapeutic agent for the control of diabetes or other blood glucose regulation disorder.
18. The method of claim 17 , further comprising:
using the dose of delivered Pramlintide and other therapeutic agent to control a blood glucose level of the patient.
19. The method of claim 18 , wherein the other therapeutic agent comprises a therapeutically effective dose of insulin.
20. The method of claim 19 , wherein the dose of insulin in the preparation is in a range from about 1 to 50 units of insulin.