COMBINATION THERAPY OF SUBSTITUTED OXAZOLIDINONES
The present invention relates to combinations of A) oxazolidinones of the formula (I) with B) acetylsalicylic acid (aspirin) and C) an ADP receptor antagonist, in particular P 2 Y 12 purinoreceptor blocker, to a process for producing these combinations and to the use thereof as medicaments, in particular for the prophylaxis and/or treatment of thromboembolic disorders.
1 . A combination comprising
A) a compound of the formula (I)
in which
R 1 is 2-thiophene which is substituted in position 5 by a radical from the group of chlorine, bromine, methyl or trifluoromethyl,
R 2 is D-A-:
where:
the radical “A” is phenylene;
the radical “D” is a saturated 5- or 6-membered heterocycle which is linked via a nitrogen atom to “A”,
which has a carbonyl group in direct vicinity to the linking nitrogen atom, and
in which a ring carbon member may be replaced by a heteroatom from the series S, N and O;
where
the group “A” defined above may optionally be substituted once or twice in the meta position relative to the linkage to the oxazolidinone by a radical from the group of fluorine, chlorine, nitro, amino, trifluoromethyl, methyl or cyano,
R 3 , R 4 , R 5 , R 6 , R 7 and R 8 are hydrogen,
the pharmaceutically acceptable salts, hydrates, prodrugs thereof or mixtures thereof
B) acetylsalicylic acid
and
C) an ADP receptor antagonist.
2 . The combination as claimed in claim 1 , characterized in that the compound A) is 5-chloro-N-({(5S)-2-oxo-3-[4-(3-oxo-4-morpholinyl)phenyl]-1,3-oxazolidin-5-yl}methyl)-2-thiophenecarboxamide of the formula
its pharmaceutically acceptable salts, hydrates, prodrugs or mixtures thereof.
3 . The combination as claimed in claim 1 , characterized in that the ADP receptor antagonist is a P 2 Y 12 purinoreceptor blocker.
4 . The combination as claimed in claim 3 , characterized in that the P 2 Y 12 purinoreceptor blocker is clopidogrel, prasugrel or cangrelor.
5 . The combination as claimed in claim 3 , characterized in that the P 2 Y 12 purinoreceptor blocker is clopidogrel.
6 . A process for producing a combination as claimed in claim 1 , characterized in that an oxazolidinone of the formula (I), acetylsalicylic acid and an ADP receptor antagonist are combined or prepared in a suitable way.
7 . A combination as claimed in any of claim 1 for the prophylaxis and/or treatment of disorders.
8 . A pharmaceutical composition comprising a combination as claimed in claim 1 further comprising one or more active pharmaceutical agents.
9 . A pharmaceutical composition comprising a combination as claimed in claim 1 and one or more pharmacologically suitable excipients and/or carriers.
10 . The use of a combination of claim 1 for producing a pharmaceutical composition for the prophylaxis and/or treatment of thromboembolic disorders.
11 . The use of a combination of claim 1 for producing a pharmaceutical composition for the prophylaxis and/or treatment of myocardial infarction with ST segment elevation (STEMI) and without ST segment elevation (non-STEMI), stable angina pectoris, unstable angina pectoris, reocclusions and restenoses following coronary interventions such as angioplasty or aortocoronary bypass, peripheral arterial occlusive diseases, pulmonary embolisms, deep vein thromboses and renal vein thromboses, transient ischemic attacks, and thrombotic and thromboembolic stroke.
12 . A method for treating a condition comprising administering a therapeutically effective amount of the combination of claim 1 .
13 . The method of claim 12 wherein the condition is a myocardial infarction with ST segment elevation (STEMI) and without ST segment elevation (non-STEMI), stable angina pectoris, unstable angina pectoris, reocclusions and restenoses following coronary interventions, peripheral arterial occlusive diseases, pulmonary embolisms, deep vein thromboses and renal vein thromboses, transient ischemic attacks, or thrombotic and thromboembolic stroke.