Granted Patent B2

US 12,201,720 · App. 17/725,677 · Granted Jan 21, 2025

Inventors: Paras Rameshlal Jain (Dayton, NJ); Sachin Vasant Chaudhari (Dayton, NJ)

Assignee: TRIS PHARMA INC

A61K9/0065A61K9/1611A61K9/1623A61K9/1635A61K9/1652A61K9/5078

Abstract

Claims (29)

1. An orally administrable drug powder composition which forms a gastro-retentive RAFT having at least two trigger pulses, the composition comprising:

(a) at least one drug in a first pulse which releases in less than about 3 hours;

(b) at least one drug in a delayed trigger release form;

(c) at least one non-toxic gas generating agent; and

(d) a RAFT system, and

wherein following oral ingestion, the composition provides a self-assembling gastro-retentive RAFT having entrapped therein, the at least one drug of (a) and (b) and the gas generated in situ by the non-toxic gas generating agent, thereby providing a floating gastro-retentive RAFT having a dual pulse system wherein at least the second pulse is a trigger pulse and which retains the at least one drug in the stomach for at least about 3 hours,

wherein the at least one drug of (a) and (b) is an active pharmaceutical ingredient (API) which is a free base or acid, or a pharmaceutically acceptable salt, solvate or hydrate, thereof,

wherein the at least one drug comprises a gamma hydroxybutyrate or its salts, hydrates, tautomers, or solvates, or mixtures thereof,

wherein the at least one delayed trigger release form of (b) comprises a pH sigmoidal delayed trigger system, an erosion delayed trigger system, a pH plus swelling delayed trigger system or a swelling delayed trigger system.

2. The orally administrable powder composition according to claim 1 , wherein the RAFT has two or more different delayed trigger pulse releases.

3. The orally administrable powder composition according to claim 1 , wherein the RAFT formed is initially at least 2 cm in size.

4. The orally administrable powder composition according to claim 1 , wherein the composition comprises two or more different RAFT systems.

5. The orally administrable powder composition according to claim 1 , wherein the raft forming system comprises at least one crosslinkable polysaccharide, at least one crosslinking agent, and at least one gas generating agent which reacts with stomach acid to form a gas.

6. The orally administrable drug composition according to claim 5 , wherein the crosslinkable polysaccharide is a galactomannan selected from guar gum, fenugreek gum, or locust bean gum and the at least one cross-linking agent selected from borax, glutaraldehyde, and/or zirconium.

7. The orally administrable drug composition according to claim 1 , wherein the RAFT comprises a gelling agent which comprises the crosslinkable polymer and crosslinking agent, wherein the gelling agent is liquid at room temperature and gels at body temperature, and is selected from xyloglucan or a poloxamer.

8. An orally administrable drug powder composition which forms a gastro-retentive RAFT having at least two trigger pulses, the composition comprising:

(a) at least one drug in a first pulse which releases in less than about 3 hours;

(b) at least one drug in a delayed trigger release form;

(c) at least one non-toxic gas generating agent; and

(d) a RAFT system, and

wherein following oral ingestion, the composition provides a self-assembling gastro-retentive RAFT having entrapped therein, the at least one drug of (a) and (b) and the gas generated in situ by the non-toxic gas generating agent, thereby providing a floating gastro-retentive RAFT having a dual pulse system wherein at least the second pulse is a trigger pulse and which retains the at least one drug in the stomach for at least about 3 hours,

wherein the RAFT is a liquid crystal RAFT comprising a cubic phase-forming lipid

wherein the at least one drug of (a) and (b) is an active pharmaceutical ingredient (API) which is a free base or acid, or a pharmaceutically acceptable salt, solvate or hydrate, thereof,

wherein the at least one drug comprises a gamma hydroxybutyrate or its salts, hydrates, tautomers, or solvates, or mixtures thereof,

wherein the at least one delayed trigger release form of (b) comprises a pH sigmoidal delayed trigger system, an erosion delayed trigger system, a pH plus swelling delayed trigger system or a swelling delayed trigger system.

9. The orally administrable drug composition according to claim 8 , wherein the gas-generating agent is selected from carbonates or bicarbonates of an alkali or alkaline earth metal, sulfites, or combinations thereof, or combinations thereof with an acid source which create a gas-generating couple.

10. The orally administrable drug composition according to claim 9 , wherein the carbonate or bicarbonate of an alkali or alkaline earth metal are selected from potassium carbonate, potassium bicarbonate, sodium carbonate, sodium bicarbonate, calcium carbonate, sodium glycine carbonate, magnesium carbonate, or aluminum carbonate.

11. The orally administrable powder composition according to claim 8 , wherein the at least one drug, selected from a gamma hydroxybutyrate or its salts, hydrates, tautomers, or solvates, or mixtures thereof, is at least sodium oxybate, calcium oxybate, magnesium oxybate, potassium oxybate, or lithium oxybate.

12. The orally administrable powder composition according to claim 1 , wherein the RAFT formed is initially at least 15 mm in width.

Assignments (3)

Continuity (3)

References Cited (185)