PHENYLALKYL N-HYDROXYUREAS FOR TREATING LEUKOTRIENE RELATED PATHOLOGIES
The method of treating patients by administering N-[3-[5-[(4-fluorophenyl)methyl]-2-thienyl]-1-methyl-2-propynyl]-N-hydroxyurea for treatment of leukotriene related pathologies, and compositions for this use.
1 . A composition comprising R- and S-enantiomers of N-[3-[5-[(4-fluorophenyl)methyl]-2-thienyl]-1-methyl-2-propynyl]-N-hydroxyurea or pharmaceutically effective salts thereof wherein the composition comprises less than 1% of the S-enantiomer.
2 . (canceled)
3 . The composition of claim 1 , wherein the composition consists of R- and S-enantiomers of N-[3-[5-[(4-fluorophenyl)methyl]-2-thienyl]-1-methyl-2-propynyl]-N-hydroxyurea or pharmaceutically effective salts thereof.
4 . The composition of claim 3 , wherein the composition consists of less than 1% of the S-enantiomer.
5 . The composition of claim 1 , wherein the composition is provided in a unit dosage form for oral administration and wherein the composition is present in an amount of about 25-100 mg.
6 . The composition of claim 5 , wherein the composition is present in an amount of about 25, 50, 75, or 100 mg.
7 . The composition of claim 5 , wherein the composition is present in an amount of about 100 mg.
8 . The composition of claim 5 , wherein said unit oral dosage form is a tablet or capsule.
9 . A method for preventing or treating a leukotriene related pathology in a subject in need thereof, comprising administering to the subject the composition of claim 1 .
10 . The method of claim 9 , wherein the subject is a human.
11 - 14 . (canceled)
15 . The method of claim 9 , wherein the pathology is atherosclerotic plaque.
16 . The method of claim 15 , wherein the method is effective in preventing or treating an acute cardiovascular event resulting from atherosclerotic plaque.
17 . The method of claim 16 , wherein the acute cardiovascular event is heart attack.
18 . The method of claim 16 , wherein the acute cardiovascular event is stroke.
19 . The method of claim 15 , wherein the subject has previously had acute coronary syndrome.
20 . The method of claim 9 , wherein the pathology is a cardiovascular disease.
21 . The method of claim 20 , wherein the cardiovascular disease is caused by atherosclerotic plaque.
22 . The method of claim 20 , wherein the cardiovascular disease results in heart attack.
23 . The method of claim 20 , wherein the cardiovascular disease results in stroke.
24 . The method of claim 20 , wherein the cardiovascular disease results in ischemia induced myocardial injury.
25 . The method of claim 20 , wherein the cardiovascular disease is peripheral arterial disease.
26 . The method of claim 20 , wherein the cardiovascular disease is acute coronary syndrome.
27 . The method of claim 20 , wherein the subject has previously had acute coronary syndrome.
28 . A pharmaceutical formulation comprising the composition of claim 1 and a pharmaceutically acceptable carrier.
29 . The pharmaceutical formulation of claim 28 , wherein the composition consists of R- and S-enantiomers of N-[3-[5-[(4-fluorophenyl)methyl]-2-thienyl]-1-methyl-2-propynyl]-N-hydroxyurea or pharmaceutically effective salts thereof.