IP Library Granted Patent US 10,682,340
Granted Patent B2
US 10,682,340 · App. 15/857,259 · Granted Jun 16, 2020

Depot formulations

Inventors: Wilma Tamraz (San Jose, CA); Huey-Ching Su (San Jose, CA); WeiQi Lin (Emerald Hills, CA); Kazuhito Yamada (Nara, JP); Naoki Matsumoto (Nara, JP); Sreenivasu Mudumba (Emeryville, CA); Komei Okabe (Nara, JP)
Assignees: DURECT CORPORATION; SANTEN PHARMACEUTICAL CO., LTD.
A61K31/436A61K9/0048A61K9/0051A61K31/355A61K47/10A61K47/14A61K47/22A61K47/26A61P27/02A61K9/0019
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Quick Facts
Patent No.
US 10,682,340
App. No.
15/857,259
Granted
Jun 16, 2020
Kind
B2
Abstract

Pharmaceutical compositions comprising an active pharmaceutical ingredient, a high viscosity liquid carrier material, a hydrophobic solvent, and a hydrophilic solvent are disclosed. Also disclosed are methods of manufacturing and using the compositions. The compositions are suitable for use, e.g., as depot formulations.

Claims (26)

1. A composition comprising:

sirolimus present in an amount ranging from about 1 wt % to about 5 wt %, based on weight of the composition;

sucrose acetate isobutyrate (SAIB) present in an amount ranging from about 0.5 wt % to about 5 wt %, based on weight of the composition;

benzyl benzoate present in an amount ranging from about 35 wt % to about 50 wt %, based on weight of the composition;

ethanol present in an amount ranging from about 1 wt % to about 10 wt %, based on weight of the composition;

polyethylene glycol (PEG) present in an amount ranging from about 40 wt % to about 50 wt %, based on weight of the composition; and

vitamin E in an amount ranging from about 0.01 wt % to about 5 wt % wherein when the composition is administered intra-ocularly as a single dose to a rabbit, a median amount of sirolimus released from the composition at 6 months after administration ranges from 30% to 100% of a total amount of the sirolimus in the composition at the time of administration.

2. The composition of claim 1 , wherein

the vitamin E is present in an amount ranging from about 0.5 wt % to about 2 wt %, based on weight of the composition.

3. The composition of claim 1 , wherein the benzyl benzoate is present in an amount ranging from about 35 wt % to about 45 wt %, based on weight of the composition.

4. The composition of claim 1 , wherein the composition has a weight ratio of SAIB:vitamin E ranging from about 0.5 to about 10.

5. The composition of claim 1 , wherein the benzyl benzoate is present in an amount ranging from about 40 wt % to about 50 wt %, based on weight of the composition.

6. The composition of claim 1 , wherein the ethanol is present in an amount ranging from about 1 wt % to about 7 wt %, based on weight of the composition.

7. The composition of claim 1 , wherein the ethanol is present in an amount ranging from about 3 wt % to about 10 wt %, based on weight of the composition.

8. The composition of claim 1 , wherein at least 98% of the sirolimus in the composition remains after storage in a 2 mL crimp sealed glass vial for 18 weeks at 5° C./60% RH.

9. The composition of claim 1 , wherein at least 90% of the sirolimus in the composition remains after storage in a 2 mL crimp sealed glass vial for 18 weeks at 25° C./60% RH.

10. The composition of claim 1 , wherein a weight ratio of SAIB to vitamin E ranges from about 60:1 to about 1:2.

11. The composition of claim 1 , wherein a weight ratio of SAIB to vitamin E ranges from about 10:1 to about 1:1.8.

12. The composition of claim 1 , wherein a weight ratio of SAIB to vitamin E ranges from about 5:1 to about 1:1.5.

13. The composition of claim 1 , wherein a weight ratio of SAIB to vitamin E ranges from about 2:1 to about 1:1.5.

14. The composition of claim 1 , wherein the composition has a density at 25° C. and 1 atmosphere ranging from 1.02 g/mL to 1.15 g/mL.

15. The composition of claim 1 , wherein the composition has a viscosity ranging from about 1 cP to about 150 cP at 25° C. and 1 atmosphere.

16. The composition of claim 1 , wherein the composition has a viscosity ranging from about 5 cP to about 50 cP at 25° C. and 1 atmosphere.

17. The composition of claim 1 , wherein the composition has a viscosity ranging from about 10 cP to about 30 cP at 25° C. and 1 atmosphere.

18. The composition of claim 1 , wherein the vitamin E is present in an amount ranging from about 0.1 wt % to about 5 wt %, based on weight of the composition.

19. The composition of claim 1 , wherein the vitamin E is present in an amount ranging from about 0.02 wt % to about 0.09 wt %, based on weight of the composition.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 17, 2018
From: TAMRAZ, WILMA; SU, HUEY-CHING; LIN, WEIQI; YAMADA, KAZUHITO; MATSUMOTO, NAOKI; MUDUMBA, SREENIVASU; OKABE, KOMEI
To: DURECT CORPORATION; SANTEN PHARMACEUTICAL CO., LTD.
Reel/Frame 045565/0081 →
Continuity (4)
Continuation 15637401 · Jun 29, 2017
Provisional Application 62440658 · Dec 30, 2016
Provisional Application 62356613 · Jun 30, 2016
Related Publication 20180117016A1 · May 3, 2018
Cited By (1)
US 12,329,748