IP Library Granted Patent US 7,067,151
Granted Patent B1
US 7,067,151 · App. 09/606,629 · Granted Jun 27, 2006

Controlled absorption diltiazem pharmaceutical formulation

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Quick Facts
Patent No.
US 7,067,151
App. No.
09/606,629
Granted
Jun 27, 2006
Kind
B1
Abstract

A controlled absorption diltiazem pellet formulation for oral administration comprises a core having diltiazem or a pharmaceutically acceptable salt thereof as the active ingredient. The core is surrounded by a coating which has only a single layer which is comprised of a relatively major proportion of talc and relatively minor proportion of sodium lauryl sulfate admixed with a minor proportion of a pharmaceutically acceptable film-forming, first polymer permeable to water and diltiazem, and a major proportion of a pharmaceutically acceptable film-forming, second polymer that is less permeable to water and diltiazem than the first polymer. The core and the coating layer both exclude organic acids. The composition of the coating layer as well as the proportion of core to coating layer are effective to permit release of the diltiazem allowing controlled absorption following oral administration. By combining short lag and long lag pellets into a single formulation, the release of diltiazem is controlled over a twenty four hour period.

Claims (55)

1. A long lag pellet suitable for use in a once-a-day diltiazem formulation comprising a core and a coating layer sufficiently enveloping the core, wherein

1) the core comprises an effective amount of diltiazem or a pharmaceutically acceptable salt and is substantially free of organic acid; and

2) the long lag pellet substantially exhibits the following dissolution profile when measured according to U.S. Pharmacopoeia XXII in a type 2 dissolution apparatus at 37° C. in 0.1N HCl at 100 rpm;

a) 0 to 10% of the diltiazem is released after 2 hours;

b) 0 to 10% of the diltiazem is released after 4 hours;

c) 0 to 15% of the diltiazem is released after 6 hours;

d) 0 to 15% of the diltiazem is released after 8 hours;

e) 4.5% to 24.5% of the diltiazem is released after 14 hours;

f) 41% to 61% of the diltiazem is released after 16 hours; and

g) more than 60% of the diltiazem is released after 18 hours.

2. A long lag pellet suitable for use in a once-a-day diltiazem formulation comprising a core and a coating layer sufficiently enveloping the core, wherein

1) the core comprises an effective amount of diltiazem or a pharmaceutically acceptable salt and is substantially free of organic acid; and

2) the long lag pellet substantially exhibits the following dissolution profile when measured according to U.S. Pharmacopoeia XXII in a type 2 dissolution apparatus at 37° C. in 0.1N HCl at 100 rpm;

a) 0 to 10.3% of the diltiazem is released after 2 hours;

b) 0 to 10.5% of the diltiazem is released after 4 hours;

c) 0 to 10.7% of the diltiazem is released after 6 hours;

d) 0 to 10.9% of the diltiazem is released after 8 hours;

e) 4.5% to 24.5% of the diltiazem is released after 14 hours;

f) 41% to 61% of the diltiazem is released after 16 hours; and

g) more than 60% of the diltiazem is released after 18 hours.

3. A once-a-day diltiazem formulation for oral administration comprising a mixture of two types of pellets, one of which is a long lag pellet that comprises a core and a coating layer sufficiently enveloping the core, wherein

1) the core comprises an effective amount of diltiazem or a pharmaceutically acceptable salt and is substantially free of organic acid; and

2) the long lag pellet substantially exhibits the following dissolution profile when measured according to U.S. Pharmacopoeia XXII in a type 2 dissolution apparatus at 37° C. in 0.1N HCl at 100 rpm;

a) 0 to 10% of the diltiazem is released after 2 hours;

b) 0 to 10% of the diltiazem is released after 4 hours;

c) 0 to 15% of the diltiazem is released after 6 hours;

d) 0 to 15% of the diltiazem is released after 8 hours;

e) 4.5% to 24.5% of the diltiazem is released after 14 hours;

f) 41% to 61% of the diltiazem is released after 16 hours; and

g) more than 60% of the diltiazem is released after 18 hours.

4. A once-a-day diltiazem formulation for oral administration comprising a mixture of two types of pellets one of which is a long lag pellet that comprises a core and a coating layer sufficiently enveloping the core, wherein

1) the core comprises an effective amount of diltiazem or a pharmaceutically acceptable salt and is substantially free of organic acid; and

2) the long lag pellet substantially exhibits the following dissolution profile when measured according to U.S. Pharmacopoeia XXII in a type 2 dissolution apparatus at 37° C. in 0.1N HCl at 100 rpm;

a) 0 to 10.3% of the diltiazem is released after 2 hours;

b) 0 to 10.5% of the diltiazem is released after 4 hours;

c) 0 to 10.7% of the diltiazem is released after 6 hours;

d) 0 to 10.9% of the diltiazem is released after 8 hours;

e) 4.5% to 24.5% of the diltiazem is released after 14 hours;

f) 41% to 61% of the diltiazem is released after 16 hours; and

g) more than 60% of the diltiazem is released after 18 hours.

5. A long lag pellet according to claims 1 through 4 where 14.5% to 24.5% of the diltiazem is released after 14 hours.

6. A long lag pellet according to claims 1 through 4 where 51% to 61% of the diltiazem is released after 16 hours.

7. A long lag pellet according to claims 1 through 4 where 41% to 51% of the diltiazem is released after 16 hours.

8. A long lag pellet according to claims 1 through 4 where 14.5% to 24.5% of the diltiazem is released after 14 hours and 51% to 61% of the diltiazem is released after 16 hours.

9. A long lag pellet according to claims 1 through 4 where 14.5% to 24.5% of the diltiazem is released after 14 hours and 41% to 51% of the diltiazem is released after 16 hours.

10. A long lag pellet according to claims 1 through 4 where

a) 0-10.3% of the diltiazem is released after 1 hour;

b) 0-11.3% of the diltiazem is released after 10 hours; and

c) 0-13.1% of the diltiazem is released after 12 hours.

11. A long lag pellet according to claims 1 through 4 where

a) 0-10.3% of the diltiazem is released after 1 hour;

b) 0-11.3% of the diltiazem is released after 10 hours;

c) 0-13.1% of the diltiazem is released after 12 hours;

d) 14.5% to 24.5% of the diltiazem is released after 14 hours; and

e) 51% to 61% of the diltiazem is released after 16 hours.

Assignments (10)
CORRECTIVE ASSIGNMENT TO CORRECT THE ASSIGNEE NAME PREVIOUSLY RECORDED ON REEL 029229, FRAME 0836. Recorded Dec 7, 2012
From: DEUTSCHE BANK AG, LONDON BRANCH
To: ACTAVIS ELIZABETH LLC
Reel/Frame 029459/0297 →
RELEASE OF SECURITY INTEREST IN INTELLECTUAL PROPERTY Recorded Nov 1, 2012
From: DEUTSCHE BANK AG, LONDON BRANCH
To: ACTAVIS GROUP PTC EHF
Reel/Frame 029227/0314 →
RELEASE OF SECURITY INTEREST IN INTELLECTUAL PROPERTY Recorded Nov 1, 2012
From: DEUTSCHE BANK AG, LONDON BRANCH
To: ACTAVIS GROUP LLC
Reel/Frame 029229/0836 →
PATENT SECURITY AGREEMENT SUPPLEMENT Recorded Dec 10, 2010
From: ACTAVIS GROUP PTC EHF.
To: DEUTSCHE BANK AG, LONDON BRANCH
Reel/Frame 025463/0758 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Feb 4, 2008
From: F.H. FAULDING & CO. LIMITED
To: PUREPAC PHARMACEUTICAL CO.
Reel/Frame 020451/0871 →
CONVERSION Recorded Feb 4, 2008
From: PUREPAC PHARMACEUTICAL CO.
To: ACTAVIS ELIZABETH LLC
Reel/Frame 020451/0919 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Dec 6, 2007
From: HEINICKE, GRANT WAYNE; LEPORE, ANGELO; MORELLA, ANGELO MARIO
To: F.H. FAULDING & CO., LTD.
Reel/Frame 020234/0804 →
GRANT OF SECURITY INTEREST Recorded Nov 28, 2007
From: ACTAVIS ELIZABETH LLC, A LIMITED LIABILITY COMPANY
To: DEUTSCHE BANK AG, LONDON BRANCH, AS SECURITY AGENT
Reel/Frame 020540/0425 →
RELEASE OF SECURITY INTEREST Recorded Nov 4, 2005
From: BANK OF AMERICA, N.A.
To: PUREPAC PHARMACEUTICAL CO.
Reel/Frame 016722/0849 →
SECURITY AGREEMENT Recorded Feb 15, 2002
From: US ORAL PHARMACEUTICALS PTY LTD; PUREPAC PHARMACEUTICALS CO.; FAULDING PHARMACEUTICALS INC.
To: BANK OF AMERICA, N.A.
Reel/Frame 012631/0017 →