Drug – bio-affecting and body treating compositions – Designated organic active ingredient containing – Heterocyclic carbon compounds containing a hetero ring...
Reexamination Certificate
2002-05-30
2003-07-15
Cook, Rebecca (Department: 1614)
Drug, bio-affecting and body treating compositions
Designated organic active ingredient containing
Heterocyclic carbon compounds containing a hetero ring...
Reexamination Certificate
active
06593329
ABSTRACT:
This application is a national stage filing of PCT International Application No. PCT/FI00/00592, filed on Jun. 29, 2000, which published in the English language. This application also claims the benefit of priority to patent application no. 9915179.1, filed in Great Britain on Jun. 29, 1999.
TECHNICAL FIELD
The present invention relates to a method for the treatment or prevention of coronary graft vasospasm after coronary artery by-pass surgery by administering levosimendan, or (−)-[[4-(1,4,5,6-tetrahydro-4-methyl-6-oxo-3-pyridazinyl)phenyl]-hydrazonopropanedinitrile (I), or pharmaceutically acceptable salts thereof, to a patient in need of such prevention or treatment.
BACKGROUND OF THE INVENTION
Levosimendan, which is the (−)-enantiomer of [[4-(1,4,5,6-tetrahydro-4-methyl-6-oxo-3-pyridazinyl)phenyl]hydrazono]propanedinitrile, and the method for its preparation is described in EP 565546 B 1. Levosimendan is potent in the treatment of heart failure and has significant calcium dependent binding to troponin. Levosimendan is represented by the formula:
The hemodynamic effects of levosimendan in man are described in Sundberg, S. et al., Am. J. Cardiol., 1995; 75: 1061-1066 and in Lilleberg, J. et al., J. Cardiovasc. Pharmacol., 26(Suppl.1), S63-S69, 1995. Pharmacokinetics of levosimendan in man after i.v. and oral dosing is described in Sandell, E.-P. et al., J. Cardiovasc. Phannacol., 26(Suppl.1), S57-S62, 1995. The use of levosimendan in the treatment of myocardial ischemia is described in WO 93/21921. Clinical studies have confirmed the beneficial effects of levosimendan in heart failure patients.
Coronary artery disease (CAD) is very common, particularly in older age groups. One of the main therapies of symptomatic CAD is coronary surgery. This is relatively simple and cost-effective treatment of main artery occlusions. However, in many patients coronaries are affected by multiple occlusions. In these cases, the availability of intact vessel for grafts becomes an issue and quite often the grafts are stretched to make anastomoses over the whole affected area Surgical manipulation of the vascular graft or its stretching, however, may induce a vasospasm that may complicate the blood flow to the reperfused areas. Sometimes the occlusion caused by the spasm is so severe that emergency surgery has to be carried out to prevent myocardial infarction.
At the moment, there are no well established treatments of coronary graft vasospasms. In some centers, calcium antagonists are used. They, however, due to their negative inotropic properties, may reduce cardiac output and induce a postoperative heart failure. Drugs having ability to prevent graft vasospasms would be very useful in the postoperative management of patients who undergo coronary artery by-pass grafting.
SUMMARY OF THE INVENTION
It has now been found that levosimendan is able to prevent coronary graft vasospasm after coronary artery by-pass surgery.
Therefore, the present invention provides the use of (−)-[[4-(1,4,5,6-tetrahydro-4-methyl-6-oxo-3-pyridazinyl)phenyl]hydrazono]propanedinitrile or a pharmaceutically acceptable salt thereof in the manufacture of a medicament for the treatment or prevention of coronary graft vasospasm.
The present invention also provides a method for the treatment or prevention of coronary graft vasospasm in a patient, said method comprising administering to a patient in need thereof an effective amount of (−)-[[4-(1,4,5,6-tetrahydro-4-methyl-6-oxo-3-pyridazinyl)phenyl]hydrazono]propanedinitrile or a pharmaceutically acceptable salt thereof.
DETAILED DESCRIPTION
The method of the invention comprises a step of administering to a subject an amount of levosimendan effective to prevent coronary graft vasospasm. The administration can be effected enterally, e.g. orally or rectally, or parenterally, e.g. intravenously or transdermally. The effective amount of levosimendan to be administered to a subject depends upon the condition to be treated, the route of administration, age, weight and the condition of the patient. In general levosimendan is administered orally to man in daily dose from about 0.1 to 20 mg, preferably from 0.2 to 15 mg, more preferably from 0.5 to 10 mg, given once a day or divided into several doses a day, depending on the age, body weight and condition of the patient. Levosimendan can be administered by intravenous infusion using the infusion rate typically from about 0.01 to 10 &mgr;g/kg/min, more typically from about 0.02 to 5 &mgr;g/kg/min. For example, using an infusion of 24 hours a rate of 0.05-0.2 &mgr;g/kg/min is considered suitable.
Levosimendan can be administered to a patient before, during or after the bypass operation. Preferably the administration of levosimendan is started, e.g. intravenously with the infusion range as described above, after the coronary bypasses are completed and the patient is weaned from the heart-lung machine. Preferably, the infusion of levosimendan is continued throughout the early recovery period, i.e. till the patient is extubated to prevent coronary graft vasospasm.
Levosimendan is formulated into dosage forms suitable for the treatment or prevention of coronary graft vasospasm using the principles known in the art. It is given to a patient as such or preferably in combination with suitable pharmaceutical excipients in the form of tablets, dragees, capsules, suppositories, emulsions, suspensions or solutions whereby the contents of the active compound in the formulation is from about 0.5 to 100% per weight. Choosing suitable ingredients for the composition is a routine for those of ordinary skill in the art. It is evident that suitable carriers, solvents, gel forming ingredients, dispersion forming ingredients, antioxidants, colours, sweeteners, wetting compounds, release controlling components and other ingredients normally used in this field of technology may be also used.
For oral administration in tablet form, suitable carriers and excipients include e.g. lactose, corn starch, magnesium stearate, calcium phosphate and talc. For oral administration in capsule form, useful carriers and excipients include e.g. lactose, corn starch, magnesium stearate and talc. For controlled release oral compositions release controlling components can be used. Typical release controlling components include hydrophilic gel forming polymers such as hydroxypropylmethyl cellulose, hydroxypropyl cellulose, carboxymethyl celluloses, alginic acid or a mixture thereof; vegetable fats and oils including vegetable solid oils such as hydrogenated soybean oil, hardened castor oil or castor seed oil (sold under trade name Cutina HR), cotton seed oil (sold under the trade names Sterotex or Lubritab) or a mixture thereof; fatty acid esters such as triglycerides of saturated fatty acids or their mixtures e.g. glyceryl tristearates, glyceryl tripalmitates, glyceryl trimyristates, glyceryl tribehenates (sold under the trade name Compritol) and glyceryl palmitostearic acid ester.
Tablets can be prepared by mixing the active ingredient with the carriers and excipients and compressing the powdery mixture into tablets. Capsules can be prepared by mixing the active ingredient with the carriers and excipients and placing the powdery mixture in capsules, e.g. hard gelatin capsules. Typically a tablet or a capsule comprises from about 0.1 to 10 mg, more typically 0.2 to 5 mg, of levosimendan.
Formulations suitable for intravenous administration such as injection or infusion formulation, comprise sterile isotonic solutions of levosimendan and vehicle, preferably aqueous solutions. Typically an intravenous infusion solution comprises from about 0.01 to 0.1 mg/ml of levosimendan.
Salts of levosimendan may be prepared by known methods. Pharmaceutically acceptable salts are useful as active medicaments, however, preferred salts are the salts with alkali or alkaline earth metals.
REFERENCES:
patent: 0 565 546 (1993-10-01), None
patent: 92/12135 (1992-07-01), None
patent: 93/21921 (1993-11-0
Lehtonen Lasse
Papp Julius
Szecsi Janos
Cook Rebecca
Finnegan Henderson Farabow Garrett & Dunner LLP
Orion Corporation
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