Menaquinol compositions and methods of treatment
AssigneeEpizon Pharma, Inc.
InventorsKeith E. Drouet, James A. Tumlin, John M. Rudey
Life of this patent
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Abstract
The present application discloses methods for the efficient preparation of high purity compounds of the Formula I, and their methods of use.
Claims21
A method of treating, preventing, slowing the progression of, arresting, and/or reversing calciphylaxis in a mammal in need thereof, the method comprising administering to the mammal a therapeutically effective amount of a composition comprising substantially pure menaquinol compound of the Formula I:
- and a pharmaceutically acceptable excipient, to prevent, slow the progression of, arrest, or reverse calciphylaxis, wherein:
- m is 7, 8, 9 or 10;
- R1 and R2 are both the residue 15;
- R1 and R2 are both the residue 16;
- R1 and R2 are both the residue 17;
- R1 and R2 are both the residue 18;
- R1 and R2 are both the residue 20;
- R1 and R2 are both the residue 21;
- R1 and R2 are both the residue 22;
- R1 and R2 are both the residue 23;
- R1 and R2 are both the residue 24;
- R1 and R2 are both the residue 25;
- R1 and R2 are both the residue 26;
- R1 and R2 are both the residue 27;
- R1 and R2 are both the residue 28;
- R1 is H and R2 is the residue 15;
- R2 is H and R1 is the residue 15;
- R1 is H and R2 is the residue 16;
- R2 is H and R1 is the residue 16;
- R1 is H and R2 is the residue 17;
- R2 is H and R1 is the residue 17;
- R1 is H and R2 is the residue 18;
- R2 is H and R1 is the residue 18;
- R1 is H and R2 is the residue 20;
- R2 is H and R1 is the residue 20;
- R1 is H and R2 is the residue 21;
- R2 is H and R1 is the residue 21;
- R1 is H and R2 is the residue 22;
- R2 is H and R1 is the residue 22;
- R1 is H and R2 is the residue 23;
- R2 is H and R1 is the residue 23;
- R1 is H and R2 is the residue 24;
- R2 is H and R1 is the residue 24;
- R1 is H and R2 is the residue 25;
- R2 is H and R1 is the residue 25;
- R1 is H and R2 is the residue 26;
- R2 is H and R1 is the residue 26;
- R1 is H and R2 is the residue 27;
- R2 is H and R1 is the residue 27;
- and
- R1 is H and R2 is the residue 28;
- R2 is H and R1 is the residue 28;
A method of treating calciphylaxis in a mammal in need thereof, the method comprising administering to the mammal a therapeutically effective amount of a composition comprising substantially pure menaquinol compound of the Formula I:
- and a pharmaceutically acceptable excipient, to treat calciphylaxis, wherein:
- m is 7, 8, 9 or 10;
- R1 and R2 are both the residue 15;
- R1 and R2 are both the residue 16;
- R1 and R2 are both the residue 17;
- R1 and R2 are both the residue 18;
- R1 and R2 are both the residue 20;
- R1 and R2 are both the residue 21;
- R1 and R2 are both the residue 22;
- R1 and R2 are both the residue 23;
- R1 and R2 are both the residue 24;
- R1 and R2 are both the residue 25;
- R1 and R2 are both the residue 26;
- R1 and R2 are both the residue 27;
- R1 and R2 are both the residue 28;
- R1 is H and R2 is the residue 15;
- R2 is H and R1 is the residue 15;
- R1 is H and R2 is the residue 16;
- R2 is H and R1 is the residue 16;
- R1 is H and R2 is the residue 17;
- R2 is H and R1 is the residue 17;
- R1 is H and R2 is the residue 18;
- R2 is H and R1 is the residue 18;
- R1 is H and R2 is the residue 20;
- R2 is H and R1 is the residue 20;
- R1 is H and R2 is the residue 21;
- R2 is H and R1 is the residue 21;
- R1 is H and R2 is the residue 22;
- R2 is H and R1 is the residue 22;
- R1 is H and R2 is the residue 23;
- R2 is H and R1 is the residue 23;
- R1 is H and R2 is the residue 24;
- R2 is H and R1 is the residue 24;
- R1 is H and R2 is the residue 25;
- R2 is H and R1 is the residue 25;
- R1 is H and R2 is the residue 26;
- R2 is H and R1 is the residue 26;
- R1 is H and R2 is the residue 27;
- R2 is H and R1 is the residue 27;
- and
- R1 is H and R2 is the residue 28;
- R2 is H and R1 is the residue 28;
A method of reversing calciphylaxis in a mammal in need thereof, the method comprising administering to the mammal a therapeutically effective amount of a composition comprising substantially pure menaquinol compound of the Formula I:
- and a pharmaceutically acceptable excipient, to reverse calciphylaxis, wherein:
- m is 7, 8, 9 or 10;
- R1 and R2 are both the residue 15;
- R1 and R2 are both the residue 16;
- R1 and R2 are both the residue 17;
- R1 and R2 are both the residue 18;
- R1 and R2 are both the residue 20;
- R1 and R2 are both the residue 21;
- R1 and R2 are both the residue 22;
- R1 and R2 are both the residue 23;
- R1 and R2 are both the residue 24;
- R1 and R2 are both the residue 25;
- R1 and R2 are both the residue 26;
- R1 and R2 are both the residue 27;
- R1 and R2 are both the residue 28;
- R1 is H and R2 is the residue 15;
- R2 is H and R1 is the residue 15;
- R1 is H and R2 is the residue 16;
- R2 is H and R1 is the residue 16;
- R1 is H and R2 is the residue 17;
- R2 is H and R1 is the residue 17;
- R1 is H and R2 is the residue 18;
- R2 is H and R1 is the residue 18;
- R1 is H and R2 is the residue 20;
- R2 is H and R1 is the residue 20;
- R1 is H and R2 is the residue 21;
- R2 is H and R1 is the residue 21;
- R1 is H and R2 is the residue 22;
- R2 is H and R1 is the residue 22;
- R1 is H and R2 is the residue 23;
- R2 is H and R1 is the residue 23;
- R1 is H and R2 is the residue 24;
- R2 is H and R1 is the residue 24;
- R1 is H and R2 is the residue 25;
- R2 is H and R1 is the residue 25;
- R1 is H and R2 is the residue 26;
- R2 is H and R1 is the residue 26;
- R1 is H and R2 is the residue 27;
- R2 is H and R1 is the residue 27;
- and
- R1 is H and R2 is the residue 28;
- R2 is H and R1 is the residue 28;
Dependencies are inferred from the claim text.