Compositions and Methods Using a Cardiac Glycoside

Abstract

A method of treating patients suffering from renal failure and concomitant cardiovascular disease with a low dose of the cardiac glycoside known as digoxin, and novel dosage forms to accomplish the method and to perform other uses.

Description

BRIEF DESCRIPTION OF THE DRAWINGS

FIG. 1 depicts a perspective view of an embodiment of an elongated, two segment, unscored tablet in accordance with the subject invention.

FIG. 2 depicts a perspective view of an embodiment of an elongated, two segment unscored tablet in accordance with the subject invention, the tablet marked at the middle, perpendicular to the tablet length, for guiding breakage.

FIG. 3 depicts a side view of an embodiment of an elongated, two segment tablet in accordance with the subject invention, the tablet having a score formed at the middle, perpendicular to the tablet length.

FIG. 4 depicts a side view of an embodiment of an elongated, two segment tablet in the middle, perpendicular to the tablet length.

FIG. 5 depicts a side view of an embodiment of an elongated, two segment tablet in accordance with the subject invention, the tablet having two scores, one each in opposing faces of the tablet at the middle, perpendicular to the tablet length.

FIG. 6 depicts a side view of an embodiment of an elongated, two segment tablet in accordance with the subject invention, the tablet having two parallel, eccentric scores formed in the same face, perpendicular to the tablet length.

FIG. 7 depicts a side view of an embodiment of an elongated, two segment tablet in accordance with the subject invention, the tablet having two eccentric scores, one each in opposing faces of the tablet away from the midline, perpendicular to the tablet length.

FIG. 8 depicts a side view of an embodiment of an elongated, two segment tablet in accordance with the subject invention, the tablet having a deep score formed into a single layer, at the middle, perpendicular to the tablet length.

FIG. 9 depicts a side view of an embodiment of an elongated, two segment tablet in accordance with the subject invention, the tablet having a deep score formed into both segments, at the middle, perpendicular to the tablet length.

FIG. 10 depicts a side view of an embodiment of an elongated, two segment tablet in accordance with the subject invention, the tablet having three scores in one face of the tablet, perpendicular to the tablet length.

FIG. 11 depicts a side view of an embodiment of an elongated, three segment, unscored tablet in accordance with the subject invention.

FIG. 12 depicts a side view of an embodiment of an elongated, tri-segmented tablet in accordance with the subject invention, the tablet having a score formed at the midline of the inactive interposed segment, perpendicular to the tablet length.

FIG. 13 depicts a round, two segment tablet configuration in accordance with the subject invention showing a single deep score formed therein.

FIG. 14 depicts a round, two segment scored tablet embodiment in accordance with the subject invention showing the scoring in a “cross” configuration.

FIG. 15 depicts a two segment rectangular, scored tablet embodiment in accordance with the subject invention showing the scoring in a “cross” configuration at the midlines of one face of the tablet.

FIG. 16 depicts a two segment rectangular, scored tablet embodiment in accordance with the subject invention showing the scoring in a “cross” configuration, corner-to-corner of one face of the tablet.

Claims

1. A method of treating a human patient in need of treatment with a cardiac glycoside, said method comprising enterally administering a solid dosage form containing about 60 mcg or less of said cardiac glycoside selected from the group consisting of digoxin and digitoxin.

2. The method of claim 1 wherein said patient suffers from renal failure.

3. The method of claim 1 in which said dosage form is ingested orally.

4. The method of claim 1 in which said dosage form comprises a tablet.

5. The method of claim 4 in which said tablet is scored.

6. A method of treatment using digoxin, said method comprising administering to a person in need of digoxin a daily dose of digoxin, said daily dose selected from the group consisting of about 12.5, 25, 50, 75, and 100 mcg.

7. The method of treatment as defined in claim 6 in which said dose is provided as a tablet or as an encapsulated tablet.

8. The method of treatment as defined in claim 7, said method comprising administering a whole or half of a 50 mcg tablet or encapsulated tablet.

9. The method of treatment as defined in claim 8 in which the patient suffers from chronic atrial fibrillation with all undesirably rapid ventricular response rate.

10. The method of treatment defined in claim 8 in which said patient suffers from congestive heart failure.

11. The method of claim 6 wherein said patient has anuria or a corrected creatinine clearance of approximately zero.

12. A method of administering digoxin to a patient in need of digoxin therapy who has a corrected creatinine clearance of about 5-50 mL/min/70 kg and who weighs about 40-100 kg or less, said method comprising enterally administering about 50 to about 100 mcg of digoxin daily in doses of 25 mcg or a whole multiple thereof.

13. The method of administering digoxin as defined in claim 12 in which said patient suffers from congestive heart failure.

14. The method of administering digoxin as defined in claim 12 in which said patient suffers from atrial fibrillation with an undesirably rapid ventricular response.

15. The method of administering digoxin as defined in claim 12 in which the corrected creatinine clearance is about 30-40 mL/min/70 kg and the patient's weight is about 50-60 kg.

16. A pharmaceutical tablet comprising about 120 mcg or less of digoxin as an active pharmaceutical ingredient, wherein said tablet is scored when the dosage strength of said digoxin in the tablet is between, and inclusive of about 60 mcg and about 120 mcg.

17. The pharmaceutical tablet of claim 16 wherein said tablet is scored when the dosage strength is less than about 60 mcg.

18. The pharmaceutical tablet of claim 16, said tablet comprising about 25 mcg of digoxin as an active pharmaceutical ingredient.

19. A pharmaceutical dosage form comprising a cardiac glycoside, said dosage form being breakable into divided doses, said dosage form comprising: a) a tablet formed from a single layer that has other than a circular dimension; orb) a plurality of layers or segments; orc) an elongated shape having a longest dimension and a second-longest dimension, and a ratio of the longest dimension to the second longest dimension preferably of about 1.5:1 to about 3:1; ord) a score selected from a deep score and a pattern comprising a plurality of scores; or.e) a height or width of greater than about 8 mm.

20. The pharmaceutical dosage form of claim 19 wherein said dosage form comprises a tablet.

21. The pharmaceutical dosage form of claim 19 wherein the cardiac glycoside is digoxin.

22. The pharmaceutical dosage form of claim 21, wherein said dosage form comprises about 25 micrograms to about 500 micrograms of digoxin.

23. The dosage form of claim 19, said dosage form being an elongated tablet.

24. The dosage form of claim 19, said dosage form comprising a quadrisecting score pattern, said pattern selected from the group consisting of a cross-scored pattern and the pattern comprising three parallel scores.

25. The pharmaceutical dosage form of claim 19, said dosage form comprising a plurality of segments wherein a first segment is pharmacologically active and a second segment is pharmacologically inactive.

26. The pharmaceutical dosage form of claim 25 that comprises a tablet consisting essentially of one segment comprising digoxin and one segment that is pharmacologically inactive.

27. The pharmaceutical dosage form of claim 25 having a first pharmacologically inactive segment interposed between an upper active segment and a lower active segment, wherein at least one of said upper and lower active segments comprises digoxin.

28. The pharmaceutical dosage form of claim 25 wherein said segmented dosage form is scored.

29. The pharmaceutical dosage form of claim 19 in which the dosage form further comprises a pharmacologically effective quantity of a drug other than a cardiac glycoside.

30. The pharmaceutical dosage form, of claim 27 in which one segment comprises a pharmacologically effective quantity of a cardiac glycoside and a different segment comprises a pharmacologically effective dose of a different drug.

31. The pharmaceutical dosage form of claim 19 in which the ratio of the height to the width or the width to the depth of the tablet is from about 2:1 to about 2.5:1.

32. The pharmaceutical dosage form of claim 19 in which said tablet is substantially homogeneous.

33. The pharmaceutical dosage form of claim 19 comprising a first segment containing a therapeutic quantity of digoxin and a second segment comprising a lesser quantity of digoxin.

34. The pharmaceutical dosage form of claim 19 containing an amount of digoxin in a range selected from the group consisting of from 10-750 mcg., from 25 to 500 mcg, and from 50 to 500 mcg.

35. The pharmaceutical dosage form of claim 19 wherein said dosage form has a printed mark designating a desired breaking region of said dosage form.

36. A method for treating a patient in need of cardiac glycoside therapy, said method comprising: providing a cardiac glycoside pharmaceutical dosage form as a substantially elongated tablet or having a deep score, said dosage form being readily breakable into a plurality of tablettes containing predictable quantities of said cardiac glycoside.

37. The method of claim 36, said elongated tablet having a longest dimension and a second-longest dimension, and a ratio of the longest dimension to the second longest dimension of about 1.5:1 to about 3:1.

38. The method of claim 36 wherein said cardiac glycoside is digoxin.