IP Library Granted Patent US 7,541,384
Granted Patent B2
US 7,541,384 · App. 12/245,648 · Granted Jun 2, 2009

Mesalamine suppository

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Quick Facts
Patent No.
US 7,541,384
App. No.
12/245,648
Granted
Jun 2, 2009
Kind
B2
Abstract

The present invention relates to a mesalamine rectal suppository designed to provide improved comfort of use. One embodiment of the invention is a mesalamine rectal suppository containing mesalamine and one or more pharmaceutically acceptable excipients, wherein the drug load of the suppository ranges from 35% to 50%. Another embodiment of the invention is a mesalamine rectal suppository containing from about 850 to about 1150 mg mesalamine and one or more pharmaceutically acceptable excipients, wherein the total weight of the suppository ranges from about 2250 to about 2700 mg. Yet another embodiment of the invention is a mesalamine rectal suppository comprising mesalamine having a tap density ranging from about 600 to about 800 g/L (as measured by USP <616>) and a hard fat having an ascending melting point of 32 to 35.5° C. Methods of preparing and methods of treatment with mesalamine suppositories are also provided. The invention further provides a method of determining a dissolution parameter (such as dissolution rate) of a mesalamine rectal suppository, such as a 1 g mesalamine suppository, by measuring its dissolution with USP Apparatus #2 at 40° C. and a paddle rotation speed of 125 rpm in 0.2 M phosphate buffer at a pH of 7.5.

Claims (16)

1. A mesalamine rectal suppository comprising from about 850 to about 1150 mg of mesalamine and a fatty base, wherein the mesalamine has a tap density ranging from about 600 to about 800 g/L (as measured by USP <616>), the drug load of the suppository ranges from 35% to 46%, and the suppository releases at least 75% by weight of the mesalamine within 2 hours of dissolution as measured with USP Apparatus #2 at 40° C., a paddle rotation speed of 125 rpm, and 3 sinker turns in 0.2 M phosphate buffer at a pH of 7.5.

2. The mesalamine suppository of claim 1 , wherein the amount of mesalamine ranges from about 950 to about 1050 mg.

3. The mesalamine suppository of claim 1 , wherein the fatty base is hard fat.

4. The mesalamine suppository of claim 1 , wherein the fatty base has an ascending melting point ranging from 32 to 33.5° C.

5. The mesalamine suppository of claim 1 , wherein the fatty base has an ascending melting point from 33 to 35.5° C.

6. The mesalamine suppository of claim 4 , the base is hard fat.

7. The mesalamine suppository of claim 5 , the fatty base is hard fat.

8. The mesalamine suppository of claim 1 , wherein the drug load ranges from about 39 to about 45%.

9. The mesalamine suppository of claim 8 , wherein the drug load ranges from about 41 to about 43%.

10. The mesalamine suppository of claim 1 , wherein the suppository releases at least 80% by weight of the mesalamine within 2 hours of dissolution as measured with USP Apparatus #2 at 40° C., a paddle rotation speed of 125 rpm, and 3 sinker turns in 0.2 M phosphate buffer at a pH of 7.5.

11. The mesalamine suppository of claim 1 , wherein the suppository releases at least 80% by weight of the mesalamine within 1 hour of dissolution as measured with USP Apparatus #2 at 40° C., a paddle rotation speed of 125 rpm, and 3 sinker turns in 0.2 M phosphate buffer at a pH of 7.5.

12. The mesalamine suppository of claim 1 , wherein the suppository releases at least 90% by weight of the mesalamine within 30 minutes of dissolution as measured with USP Apparatus #2 at 40° C., a paddle rotation speed of 125 rpm, and 3 sinker turns in 0.2 M phosphate buffer at a pH of 7.5.

13. A method of treating active ulcerative proctitis in a patient in need thereof comprising administering the mesalamine rectal suppository of claim 1 to the patient.

14. The method of claim 13 , wherein the mesalamine rectal suppository is administered once a day.

15. The method of claim 14 , wherein the mesalamine rectal suppository is administered once a day at bedtime.

16. The mesalamine suppository of claim 1 , wherein the suppository is a moulded suppository.

Assignments (5)
CHANGE OF NAME Recorded Mar 18, 2016
From: APTALIS PHARMA CANADA INC.
To: APTALIS PHARMA CANADA ULC
Reel/Frame 038037/0424 →
TERMINATION AND RELEASE Recorded Jan 31, 2014
From: BANK OF AMERICA, N.A., AS ADMINISTRATIVE AGENT
To: APTALIS PHARMA US, INC.; APTALIS PHARMATECH, INC.; APTALIS PHARMA CANADA INC.
Reel/Frame 032149/0111 →
PATENT SECURITY AGREEMENT Recorded Oct 31, 2013
From: APTALIS PHARMA CANADA INC.; APTALIS PHARMA US, INC.; APTALIS PHARMATECH, INC.
To: BANK OF AMERICA, N.A., AS ADMINISTRATIVE AGENT
Reel/Frame 031531/0488 →
CHANGE OF NAME Recorded Dec 16, 2011
From: AXCAN PHARMA INC.
To: APTALIS PHARMA CANADA INC.
Reel/Frame 027401/0722 →
CHANGE OF NAME Recorded Dec 13, 2011
From: AXCAN PHARMA INC.
To: AXCAN PHARMA CANADA INC.
Reel/Frame 027373/0622 →