Drug – bio-affecting and body treating compositions – Preparations characterized by special physical form – Tablets – lozenges – or pills
Reexamination Certificate
2001-02-01
2002-08-13
Page, Thurman K. (Department: 1615)
Drug, bio-affecting and body treating compositions
Preparations characterized by special physical form
Tablets, lozenges, or pills
C424S436000, C424S451000, C424S449000, C424S464000, C424S489000, C424S044000, C424S045000
Reexamination Certificate
active
06432446
ABSTRACT:
FIELD OF THE INVENTION
The invention relates to the desmethyl metabolite of 4-diethylamino-2-butynyl cyclohexylphenylglycolate and optical isomers thereof. The compound 4-diethylamino-2-butynyl cyclohexylphenylglycolate has the generic name oxybutynin (OXY) and is an approved drug for the management of urinary incontinence. The drug may also be used in patients suffering from gastrointestinal hypermotility disorders.
The compound 4-ethylamino-2-butynyl cyclohexyl-phenylglycolate, also called desethyloxybutynin (DEO), and has the following chemical structure:
BACKGROUND OF THE INVENTION
Racemic oxybutynin (OXY) is used therapeutically in the treatment of urinary incontinence due to detrusor muscle instability. The drug may also be used in patients suffering from gastrointestinal hypermotility disorders such as for example irritable bowel syndrome (IBS). OXY exerts a spasmolytic effect by inhibiting the contractions of smooth muscle with cholinergic innervation.
In patients with conditions characterized by involuntary bladder contractions, clinical studies have demonstrated that OXY increases bladder capacity, diminishes the frequency of involuntary contractions of the detrusor muscle, and delays the initial desire to void. OXY is therefore useful in the treatment and prevention of both incontinence and frequent voluntary urination.
Racemic oxybutynin consists of a 50/50 mixture of R(−)-oxybutynin and S(+)-oxybutynin. It has been shown that practically all of the anticholinergic activity of OXY resides in the R(−)-isomer, while the activity of the S(+)-isomer is due to its direct spasmolytic activity (Aberg et al. U.S. Pat. No. 5,532,278.)
One clinically important metabolite of OXY has been identified in humans after administration of OXY and is called desethyloxybutynin (DEO) (Westlin, L., 1985. Internal report, Smith & Nephew Pharmaceuticals Ltd.). A second metabolite, didesethyloxybutynin (DIDEO) has been synthesized and found to have low pharmacological activity and short duration of action (Aberg et al. to be published.) A third metabolite, called N-oxide-oxybutynin, has been suggested but may not be chemically stable (Lindeke B. et al., 1981 Metabolism of Oxybutynin . . . Biomed Mass Spectrometry. 1981, 8:506-513).
SUMMARY OF THE INVENTION
The problems of the prior art have been overcome by the present invention, which is directed to a method of treating disorders involving the urethrogentical tract by administering to pateints in need thereof therapeutically effective amounts of the desethyl metabolite of oxybutynin and/or the optically active isomers thereof, which are free from said cardiac side effect of oxybutynin, while maintaining the therapeutic activities of oxybutynin or the optically active isomers thereof.
It has now unexpectedly been found that oxybutynin causes a prolongation of the QTc-interval of the EKG. Such prolongation of the QTc-interval is known to be caused by inhibition of the delayed rectifier potassium current in cardiac cells. Furthermore, it is known that a prolongation of the QTc-interval is indicative of and strongly correlated to a fatal form of cardiac arrhythmias (ventricular fibrillation) called torsades de pointes. It has now unexpectedly been found that the desethyl metabolite of oxybutynin and the optically active isomers thereof are free from said cardiac side effect of oxybutynin, while maintaining the therapeutic activities of oxybutynin or the optically active isomers thereof.
It has also been found that certain types of drugs that utilize the same or similar metabolic enzymes as oxybutynin, will further increase the risk for torsades des pointes when combined with oxybutynin. Examples of such drugs are ketoconazole and erythromycin.
This most unwanted side effect of oxybutynin is of concern in all patients given racemic oxybutynin and particularly in patients that are of age or patients that have pre-existing cardiovascular conditions for example long basal QTc interval.
It was found that both the R(−)-isomer and the S(+)-isomer of oxybutynin cause a prolongation of the QTc-interval of the EKG, while the corresponding isomers of DEO did not cause a prolongation of the QTc-interval. Since the duration of the QTc-interval is dose-dependently prolonged by these compounds, the risk for torsades des pointes arrhythmias is exceptionally high when S(+)-oxybutynin is given to the patients, since the S-isomer is administered in higher doses than the racemate. However, racemic oxybutynin is used at a dose of 5 mg several times daily for very long time periods and the risk for prolongation of QTc by such doses is very substantial. Examples of drugs that have been found to cause prolongation of QTc and consequently might cause torsades des pointes arrhythmias are terfenadine (Seldane®), astemizole (Hismanal®) and terodiline (Micturin®); all these drugs have been withdrawn from the market because of this side effect.
DETAILED DESCRIPTION OF THE INVENTION
CHEMISTRY
Racemic oxybutynin is 4-diethylamino-2-butynyl &agr;-cyclohexyl-&agr;-hydroxybenzeneacetate, also known as 4-diethylamino-2-butynyl cyclohexylphenylglycolate and herein also referred to as OXY. The generic name given to the hydrochloride salt of racemic oxybutynin by the USAN Council is oxybutvnin chloride; it is sold under the name of Ditropan®.
Racemic desethyloxybutynin is 4-ethylamino-2-butynyl cyclohexyl-phenylglycolate and is a known metabolite of oxybutynin (Hughes K. M. et al. Measurement of oxybutynin and its N-desethyl metabolite in plasma . . . Xenobiotica, 1992, 7: 859-869). This compound is herein referred to as DEO. No generic name is known for this compound or any of its salts.
The overall process for preparing DEO involves:
(a) the preparation of the side chain 4-ethylamino-2-butynyl chloride from dichlorobutyne
(b) by standard esterification technique, reacting cyclohexylphenyl glycolic acid with 4-ethylamino-2-butynyl chloride to produce 4-ethylamino-2-butynyl cyclohexylphenyl-glycolate (DEO).
An alternative process for preparing the compound of the invention involves the preparation of a hydroxylated side chain in stead of the above mentioned halogenated side chain.
Racemic cyclohexylphenylglycolic acid is commercially available from SIPSY Chem Corp., 2137 Route 33, Suite 2, Hamilton Square, N.J. 08690.
The process for preparing R-DEO is described in U.S. Pat. No. 6,123,961 and a process for preparing S-DEO is described in U.S. Pat. No. 5,532,278, the disclosures of which are hereby incorporated by reference.
DOSING, DOSAGE FORMS, PHARMACEUTICAL COMPOSITIONS
The magnitude of a prophylactic or therapeutic dose of the compound of this invention in the acute or chronic management of disease will vary with the severity and nature of the condition to be treated and the route of administration. The dose and the frequency of the dosing will also vary according to the age, body weight and response of the individual patient. In general, the total daily dose range for the compound of this invention for the conditions described herein is from about 1 mg to about 100 mg in single or divided doses, preferably in divided doses. In managing the patient, the therapy should be initiated at a lower dose, perhaps at about 0.5 mg to about 25 mg, and may be increased up to about 200 mg depending on the patient's global response. It is further recommended that patients over 65 years and those with impaired renal or hepatic function initially receive low doses and that they be titrated based on individual response(s) and plasma drug level(s). It may be necessary to use dosages outside these ranges, as will be apparent to those skilled in the art. Further, it is noted that the clinician or treating physician will know how and when to interrupt, adjust, or terminate therapy in conjunction with individual patient response. The terms “a therapeutically effective amount” and “an amount sufficient to treat urinary incontinence but insufficient to cause adverse effects” are encompassed by the above-described dosage amounts and dose frequency schedule
Bennett Rachel M.
Bridge Pharma, Inc.
Nields & Lemack
Page Thurman K.
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