IP Library Granted Patent US 10,752,681
Granted Patent B2
US 10,752,681 · App. 15/220,249 · Granted Aug 25, 2020

Therapeutic agent preparations for delivery into a lumen of the intestinal tract using a swallowable drug delivery device

Inventor: Mir Imran (Los Altos Hills, CA)
Assignee: Rani Therapeutics, LLC
C07K16/241A61K9/0002A61M5/00A61M25/10A61K9/4808A61K2039/54A61K2039/542A61M31/002C07K2317/24
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Quick Facts
Patent No.
US 10,752,681
App. No.
15/220,249
Granted
Aug 25, 2020
Kind
B2
Abstract

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.

Claims (23)

1. A method for delivering Adalimumab into a wall of the small intestine, the method comprising:

swallowing a drug delivery device comprising a capsule, an actuator having a first configuration and a second configuration, and a solid Adalimumab preparation operably coupled to the actuator, the solid Adalimumab preparation comprising a therapeutically effective dose of Adalimumab, the preparation being contained within the capsule in the first configuration and advanced out of the capsule and into the wall of the small intestine in the second configuration so as to insert the solid Adalimumab preparation into the wall of the small intestine wherein the solid Adalimumab preparation has a tissue penetrating shape configured for penetration of the wall of the small intestine; and

actuating the actuator responsive to a condition in the small intestine to deliver the solid Adalimumab preparation into the wall of the small 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 a weight percent of Adalimumab in the preparation comprises between 8 to 12%.

5. The method of claim 1 , wherein the dose of Adalimumab in the Adalimumab preparation is in a range from 1 to 5 mg.

6. The method of claim 5 , wherein the dose of Adalimumab is in the Adalimumab preparation is in a range from 2 to 4 mg.

7. The method of claim 1 , wherein the Adalimumab preparation comprises at least one pharmaceutical excipient.

8. The method of claim 7 , wherein the at least one pharmaceutical excipient comprises at least one of a binder, a preservative or a disintegrant.

9. The method of claim 1 , further comprising retaining the Adalimumab preparation within the intestinal wall after insertion.

10. The method of claim 9 , wherein retaining comprises anchoring at least one of a barb or an inverse taper shape of the Adalimumab preparation in intestinal wall tissue.

11. The method of claim 1 , wherein delivering the Adalimumab preparation comprises applying a force to the Adalimumab preparation.

12. The method of claim 11 , wherein the Adalimumab preparation is advanced completely into the intestinal wall by such application of force.

13. The method of claim 11 , wherein the force is a mechanical force applied to a surface of Adalimumab preparation.

14. The method of claim 1 , wherein the Adalimumab preparation produces a release of Adalimumab with a t½ in a range of 6 to 24 hours.

15. The method of claim 1 , wherein the Adalimumab preparation produces a release of Adalimumab with a t½ of 40 days.

16. The method of claim 1 , further comprising:

using the dose of delivered Adalimumab to treat an autoimmune disease selected from the group consisting of rheumatoid arthritis, juvenile idiopathic arthritis, psoriatic arthritis, ankylosing spondylitis, Crohn's disease, plaque psoriasis, and ulcerative colitis.

17. The method of claim 16 , where the autoimmune disease is rheumatoid arthritis.

18. The method of claim 16 , where the autoimmune disease is psoriatic arthritis.

19. The method of claim 16 , where the autoimmune disease is ankylosing spondylitis.

20. The method of claim 16 , where the autoimmune disease is juvenile idiopathic arthritis.

Assignments (3)
RELEASE OF SECURITY INTEREST Recorded Dec 19, 2025
From: AVENUE VENTURE OPPORTUNITIES FUND, L.P.
To: RANI THERAPEUTICS, LLC
Reel/Frame 073971/0117 →
SECURITY INTEREST Recorded Aug 9, 2022
From: RANI THERAPEUTICS, LLC
To: AVENUE VENTURE OPPORTUNITIES FUND, L.P., AS AGENT
Reel/Frame 061131/0478 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 4, 2018
From: IMRAN, MIR
To: RANI THERAPEUTICS, LLC
Reel/Frame 045003/0248 →
Continuity (7)
Continuation 13538912 · Jun 29, 2012
Continuation In Part 12978233 · Dec 23, 2010
Continuation In Part 12978164 · Dec 23, 2010
Continuation In Part 12978301 · Dec 23, 2010
Provisional Application 61571642 · Jun 30, 2011
Provisional Application 61571641 · Jun 29, 2011
Related Publication 20170174758A1 · Jun 22, 2017
Cited By (2)
US 12,263,325 US 12,268,831