Drug – bio-affecting and body treating compositions – Designated organic active ingredient containing – Having -c- – wherein x is chalcogen – bonded directly to...
Reexamination Certificate
2001-05-07
2003-08-19
Jarvis, William R. A. (Department: 1614)
Drug, bio-affecting and body treating compositions
Designated organic active ingredient containing
Having -c-, wherein x is chalcogen, bonded directly to...
Reexamination Certificate
active
06608088
ABSTRACT:
FIELD OF THE INVENTION
The present invention refers to the use of acetylcholinesterase inhibitors with high specificity and selectivity for centrally active acetylcholinesterase (resulting in an increased concentration and duration of acetylcholine in brain) for preparing pharmaceutical compositions for the treatment of functional (migraine and primary fibromyalgia) and/or organic (“phantom limb” caused by tumoral or traumatic denervation or autoimmune mechanism) central pain syndromes.
BACKGROUND OF THE INVENTION
Along the years migraine has been the object of deep interest and studies in view of the importance of this pathology both for the extremely large number of patients involved and because it causes (during its more serious episodes) important or total limitations to otherwise healthy subjects.
Various theories were formulated in order to find an explanation to the origin of migraine. Among these theories we can remember the “dry theory” (according to which the pain is due to the pulsing distension of cephalic vessels), the “Wet theory” (which implies the sterile inflammation of the arterial vessels which became dilated and bloated), the “serotonin-theory” according to which the pathology is caused by a disorder of the serotoninergic system in the central nervous system.
This last theory was very successful and allowed the preparation of active principles having a serotonino-mimetic activity capable of relieving a migraine attack.
About thirty years ago an interesting article [Stoyan Iv. IKONOMOFF—Archives Suisses de Neurologie, Neurochirurgie et de Psychiatrie—Vol. 102, fascicule p. 299-312 (1968)] referred to the possibility of treating migraine by using pharmaceutical products, such as Nivaline, an alkaloid, and Syntostigmine, which were known for their acetylcholinesterase inhibiting effect.
The article proposed the use of the two above said compounds (or more generally of acetylcholinesterase inhibiting medicaments) as a possible new way for resolving migraine disorders. Unfortunately the use of the medicaments suggested in the above said word, as also of other similar compounds having the same effect, required very high dosages, the administration should be performed by injection and was responsible of various side effects which made their use difficult; therefore this way was abandoned and no indication was thereafter reported in the literature about the use of acetylcholinesterase inhibitors as medicament for the treatment of migraine. In fact even the most recent editions of fundamental text-books in Neurology and Pharmacology [see for example .Victor and Adams, McGraw-Hill, New York (last edition) and Goodman and Gilman, McGraw-Hill, New York (1996) respectively] do not report these drugs as employed or useful for treating pain, whatever its origin and mechanism.
Moreover in various studies [see for example C. Ghelardini et al.—Presynaptic auto- and hetero-receptors in the cholinergic regulation of pain—Trends In Receptor Research (Elsevier Science Publishers B.V.) (1992)] it is reported that peripherically active acetylcholinesterase inhibiting compounds are not suitable for analgesic use in man.
WO 97/29750 discloses the use of acetylcholine esterase inhibitors, including Donepezil or Metrifonate, for the treatment rheumatological diseases.
In H. M. Bryson et al.: Drugs Aging Vol. 10(3) 1997, pp. 234-239 and in G. R. Dawson et al.: Behavioural Brain Research, Vol. 57 (2) 1993, pp. 143-153, it is reported that analgesics, like morphine, can be used for causing disappearance or reduction of pain connected with disorders interesting the peripheral system.
EP-A-515302 describes the treatment of fatigue syndrome with cholinesterase inhibitor.
In EP-A413667 and U.S. Pat. No. 5,010,083 several compounds for the alleviating of pain and memory dysfunction are described.
In J. B. Press et al.: Expert Opinion Vol. 4(4), 1994, pp. 379-393 an up-date of the studies regarding opioic and non-opioid analgesia is reported.
BRIEF SUMMARY
It was now surprisingly found that acetycholinesterase inhibiting compounds with high specificity and selectivity for centrally active acetylcholinesterase can be used with excellent results in the acute, abortive or preventive, prophylactic treatment of migraine and also of other related disorders which are commonly defined as functional and/or organic neurogenic central pain syndromes.
Furthermore, the acetylcholinesterase inhibiting compounds with high specificity and selectivity for centrally active acetylcholinesterase in the present invention is defined as follows: the acetylcholinesterase inhibiting compounds having clinical indication of use such as central progressive memory deterioration in Alzheimer disease or senile dementia and which can cross the blood-brain barrier and can enter the brain in large amounts.
Other anticholinesterase agents can not be useful for treating CNS cholinergic disturbances due to acting peripheral tissues including sympathetic ganglia. Among the above said pathologies we can remember: migraine, primary fibromyalgia, pain syndromes from organic deafferentation caused by amputation (“phantom limb”), denervation or autoimmune mechanism (multiple sclerosis) or infections (zosteric postherpetic nevralgia).
DETAILED DESCRIPTION OF THE INVENTION
The acetylcholinesterase inhibitors according to the invention as above defined do not present the undesired side effects as miosis and block of accomodation reflex with resultant focusing problems in near vision, changes in the function of all the secretory glands, including lacrimal, bronchial, sweat, salivary, antral, intestinal, and acinar pancreatic glands, nausea, vomit, gastric acid hyper-secretion, abdominal pains, diarrhoea, fainting or pre-fainting sensation, disturbances of cardio-vascular functions. The administration is well tolerated by patients and allows to obtain the desired results even with a single oral administration daily.
The present invention obviously refers to pharmaceutical compositions containing as active principle an acetylcholinesterase inhibitor having central activity possibly in combination with the usual excipient used for preparing pharmaceutical composition for oral administration for the treatment of the above said pathologies.
In particular the compositions according to the invention will contain the active principle in quantities comprised between 1.5-12 mg, more preferably 5-10 mg.
The treatment can be symptomatic or chronic.
The symptomatic, acute treatment is normally performed by administering orally to the patient a single dosage containing from 0.1 to 50 mg daily, preferably 0.5 to 40 mg daily, more preferably 1 to 30 mg daily of active principle; while for the chronic treatment the same administration can be repeated once a day for 40-80 days.
Among the compounds useful according to the present invention particularly preferable are: Donepezil or a pharmacologically acceptable salt thereof, Rivastigmine or a pharmacologically acceptable salt thereof and Metrifonate.
These compounds are shown hereinafter:
Donepezil
1H-Inden-1-one, 2,3-dihydro-5,6-dimethoxy-2-[[1-(phenylmethyl)4-piperidinyl]methyl]-, hydrochloride
[Hydrochloride: CAS Registry No. 120011-70-3]
(2) Rivastigmine
Carbamic acid, ethylmethyl-, 3-[1-(dimethylamino)ethyl]phenyl ester
[CAS Registry No. 123441-03-2]
(3) Metrifonate
Phosphoric acid, (2,2,2-trichloro-1-hydroxyethyl)-, dimethyl ester
[CAS Registry No. 52-68-6]
In the present invention, the term “pharmacologically acceptable salt thereof” include the salts of inorganic acids, such as hydrochloride, hydrobromide, sulfate, nitrate and phosphate, and those of organic acids, such as formate, acetate, oxalate, succinate, maleate, fumarate, methanesulfonate, benzenesulfonate and toluenesulfonate. Among these, hydrochloride is more preferable.
In practising the present invention, the acetylcholinesterase inhibitor compounds of the present invention may be orally or parentally administered. In general, the are administered i
Nicolodi Maria
Sicuteri Federigo
Birch & Stewart Kolasch & Birch, LLP
Eisai., Ltd.
Jarvis William R. A.
LandOfFree
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