IP Library Granted Patent US 11,666,573
Granted Patent B2
US 11,666,573 · App. 16/759,287 · Granted Jun 6, 2023

Dosage regimen of paliperidone palmitate extended-release injectable suspension

Inventors: Youxin Li (Shandong, CN); Chunjie Sha (Shandong, CN); Fengjuan Zhao (Shandong, CN); Changbing Tu (Shandong, CN); Kaoxiang Sun (Shandong, CN); Wanhui Liu (Shandong, CN); Lifang Sun (Shandong, CN); Ying Meng (Shandong, CN)
Assignee: Geneora Pharma (Shijiazhuang) Co., Ltd.
A61K31/519A61K9/0019
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Quick Facts
Patent No.
US 11,666,573
App. No.
16/759,287
Granted
Jun 6, 2023
Kind
B2
Abstract

Provided herein are simplified dosing regimens for administering paliperidone palmitate to a patient in need of treatment of schizophrenia or schizoaffective disorders.

Claims (34)

1. A dosing regimen for administering paliperidone palmitate to a patient in need of treatment of schizophrenia or schizoaffective disorders, the dosing regimen consisting of:

(1) administering intramuscularly to the patient an initial loading dose of 312 mg-468 mg paliperidone palmitate on the first day of treatment; and

(2) beginning on the 29th day±7 days from the initial loading dose, administering intramuscularly to the patient at least one monthly maintenance dose in the range of 39 mg to 234 mg paliperidone palmitate, wherein each dose of paliperidone palmitate is formulated in an aqueous suspension formulation.

2. The dosing regimen of claim 1 , wherein the initial loading dose comprises 351 mg paliperidone palmitate.

3. The dosing regimen of claim 1 , wherein the at least one monthly maintenance dose includes a first monthly maintenance dose of 78 mg-234 mg paliperidone palmitate following the initial loading dose.

4. The dosing regimen of claim 3 , wherein the first monthly maintenance dose following the initial loading dose comprises 156 mg paliperidone palmitate.

5. The dosing regimen of claim 3 , wherein the at least one monthly maintenance dose includes, subsequent to the first monthly maintenance dose, one or more further monthly maintenance doses in the range of 39 mg-234 mg paliperidone palmitate.

6. The dosing regimen of claim 5 , wherein each of the one or more further monthly maintenance doses is 117 mg paliperidone palmitate.

7. The dosing regimen of claim 1 , wherein the paliperidone palmitate is in the form of submicron-sized particles having specific surface areas in the range of 2-8 m 2 /g.

8. The dosing regimen of claim 1 , wherein the paliperidone palmitate is in the form of submicron-sized particles having specific surface areas in the range of 10-15 m 2 /g.

9. The dosing regimen of claim 1 as a monotherapy.

10. The dosing regimen of claim 1 as an adjunct therapy to antidepressant or mood stabilizer.

11. The dosing regimen of claim 1 , wherein the aqueous suspension formulation for each dose comprises:

(a) from 3 to 20% (w/w) of the paliperidone palmitate having a mass median diameter (d(0.5)) in the range of 900 nm-1.2 μm;

(b) from 0.5 to 3% (w/w) of polysorbate 20;

(c) from 0.5 to 4% (w/w) of polyethylene glycol 4000; and

(d) up to 2% (w/w) preservatives; and

(e) water q.s. ad 100%, wherein the formulation has a pH in the range of 7-8.5.

12. The dosing regimen of claim 11 , wherein the aqueous suspension composition for each dose comprises, by w/w %,

15.04% of paliperidone palmitate;

0.48% of citric acid monohydrate;

0.48% disodium hydrogen phosphate anhydrous;

0.24% sodium dihydrogen phosphate monohydrate;

0.27% sodium hydroxide;

2.89% polyethylene glycol 4000;

1.16% polysorbate 20; and

79.43% water.

13. A dosing regimen for administering paliperidone palmitate to a patient in need of treatment of schizophrenia or schizoaffective disorders, the dosing regimen comprising:

(1) administering intramuscularly to the patient an initial loading dose of 312 mg-468 mg paliperidone palmitate on the first day of treatment; and

(2) beginning on the 29 th day±7 days from the initial loading dose, administering intramuscularly to the patient a first monthly maintenance dose in the range of 39 mg-234 mg paliperidone palmitate without administering any dose between the initial loading dose and the first monthly maintenance dose, wherein each dose of paliperidone palmitate is formulated in an aqueous suspension formulation.

14. The dosing regimen of claim 13 , wherein the initial loading dose comprises 351 mg paliperidone palmitate.

15. The dosing regimen of claim 13 , wherein the first monthly maintenance dose comprises 156 mg paliperidone palmitate.

16. The dosing regimen of claim 13 further comprising, subsequent to the first monthly maintenance dose, one or more further monthly maintenance doses in the range of 39 mg-234 mg paliperidone palmitate.

17. The dosing regimen of claim 16 , wherein each of the one or more further monthly maintenance doses is 117 mg paliperidone palmitate.

Assignments (3)
CHANGE OF NAME Recorded Aug 30, 2024
From: GENEORA PHARMA (SHIJIAZHUANG) CO., LTD.
To: LUYE INNOMIND PHARMA SHIJIAZHUANG CO., LTD.
Reel/Frame 068823/0161 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 24, 2023
From: SHANDONG LUYE PHARMACEUTICAL CO., LTD.
To: GENEORA PHARMA (SHIJIAZHUANG) CO., LTD.
Reel/Frame 063090/0338 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 28, 2020
From: LI, YOUXIN; SHA, CHUNJIE; ZHAO, FENGJUAN; TU, CHANGBING; SUN, KAOXIANG; LIU, WANHUI; SUN, LIFANG; MENG, YING
To: SHANDONG LUYE PHARMACEUTICAL CO., LTD.
Reel/Frame 052507/0734 →
Continuity (3)
Provisional Application 62647333 · Mar 23, 2018
Provisional Application 62578082 · Oct 27, 2017
Related Publication 20200297729A1 · Sep 24, 2020