Drug – bio-affecting and body treating compositions – Designated organic active ingredient containing – Nitrogen containing other than solely as a nitrogen in an...
Reexamination Certificate
2001-06-25
2003-02-11
Carr, Deborah D. (Department: 1621)
Drug, bio-affecting and body treating compositions
Designated organic active ingredient containing
Nitrogen containing other than solely as a nitrogen in an...
C554S035000, C554S079000, C562S512000, C564S192000
Reexamination Certificate
active
06518311
ABSTRACT:
FIELD OF THE INVENTION
The present invention relates to methods for the treatment of pain. More particularly, the invention relates to the use of certain branched-chain fatty acids (BFAs) and derivatives thereof in the treatment of pain in mammals and in particular in humans.
BACKGROUND OF THE INVENTION
Pain is a complex sensation and is the most common symptom of disease. Pain which is classified as somatogenic may be nociceptive pain which is due to a noxious stimulus (chemical, thermal, mechanical etc.) that activates pain receptors , or neuropathic pain which results from dysfunction of the central or peripheral nervous system and is often poorly localized.
Pain may also be classified as being acute or chronic in nature. Acute pain is usually a result of injury (e.g. trauma or disease), it lasts a short time and is typically resolves as the injured tissue heals or soon after. Chronic pain is usually defined broadly and arbitrarily as a pain persisting for over one month beyond the resolution of an acute tissue injury, pain persisting or recurring for more than 3 months, or pain associated with tissue injury that is continued or progressed [The Merck Manual, 1999].
Several pain syndromes are difficult to classify according to these criteria. These include, for example, chronic headache and continuous acute pain produced by the invasion of body tissues in malignant diseases.
Neuropathic pain is a common type of pain which can develop after injury to the nervous system and is usually a chronic pain. Neuropathic pain may result by trauma, central nervous system (CNS) pathology (e.g. stroke, spinal cord injury), by diseases such as diabetes, herpes zoster, or late stage of cancer, or by chemical injury. It may also develop after amputation.
The long-lasting neural mechanisms associated with chronic pain differ from those observed in acute pain [Loeser and Melzack (1999) Lancet 353: 1607-9]. Accordingly, also the pharmaceutical agents used to treat the various pain syndromes are different. It is well known that drugs that are useful against acute pain may be ineffective against chronic pain and drugs active, for example, against neuropathic pain may not be effective analgesics in other kinds of pain.
A variety of analgesic agents have been demonstrated as useful in the treatment of pain symptoms. Yet so far, the majority of available analgesics possess undesirable side effects.
Opioids are substances that act as agonists of opioid receptors in the CNS, and are considered as the most potent analgesic agents. Agents such as morphine and related opioid compounds, are often required for relief of severe pain. However, these narcotic drugs have the severe drawback of leading to dependence and addiction. In addition, patients treated with opioids tend to develop tolerance to the drug, which leads to increasing dosage of the drug needed for exerting the analgesic effect and to subsequent withdrawal symptoms. Further side effects associated with opioid drugs include nausea, sedation and respiratory depression.
Nonopioid analgesics, e.g. cyclooxygenase inhibitors such as acetaminophen (=paracetamol) and nonsteroidal anti-inflammatory drugs (NSAIDs) are often effective for treatment of mild to moderate pain. Anti-inflammatory agents of the NSAID class such as acetylsalicylic acid (aspirin), indomethacin, diclofenac and benzydamine have been used as analgesics in pain associated with trauma and inflammation. Nevertheless, clinical trials are still inconclusive. Common side effects of the NSAID class of drugs include: gastrointestinal irritation and ulceration, blockade of platelet aggregation, renal dysfunction and hepatic damage.
Another major class of analgesics is the local anaesthetics that block sodium channels. Compounds of this class, e.g. lidocaine, when topically applied to the spine, have been found effective for control of pain after surgery or trauma, but require expertise and infrastructure to administer and monitor properly. Systemic infusion of lidocaine can reduce acute pain, but requires continuous monitoring so that resuscitation from seizures or apnea can be performed immediately.
N-methyl-D-aspartate (NMDA) receptor antagonists are useful in treating neuropathic pain. It has been found that several sites on the NMDA receptor complex, activated by the excitatory amino acid glutamate, are analgesic targets. For example, Ketamine, which blocks the open calcium channel within this complex, has been suggested for use preoperatively or in neuropathic pain. Clinical studies confirm ketamine's merit as an analgesic or co-analgesic (e.g. with morphine). Nevertheless, psychotomimetic and other side effects such as salivation or cardiac stimulation restrict the applicability of standard doses of ketamine [Martindale: The Extra Pharmacopeia. 31
st
Edition. London: Pharmaceutical Press, (Editor Reynolds) 1996, pg. 1258-9].
Antidepressants, e.g. the tricyclic antidepressants amitriptyline and imipramine, and the serotonin re-uptake inhibitor paroxetine, have also been proven beneficial as analgesics. Tricyclic antidepressants can be helpful in several chronic pain states, especially in patients with head pain (including headache), central pain, and neuropathic pain. However, these drugs have the potential for adverse side effects, including anticholinergic effects and life-threatening cardiovascular effects.
Anticonvulsants have also been found to have useful analgesic effects. Gabapentin, has shown promise for the treatment of chronic pain [Rowbotham et al. (1998) JAMA 280: 1837-42] and carbamazepine and phenytoin, can be effective in the treatment of a range of neuropathic pain states. In particular, it has been found that trigeminal neuralgia responds well to carbamazepine [Green and Selman (1991) Headache 31: 588-592]. Sodium valproate has been reported as being effective in the prophylactic treatment of migraine [Hering & Kuritzky (1992) Cephalalgia 12: 81-84]. However, sodium valproate was found ineffective in the placebo controlled study in treating postoperative pain, which is an acute pain [Martin et al. (1988)
Ann FrAnesth Reanim
7:387-92]. Some analogs of valproic acid that have been tested as potential anticonvulsant drugs were found sedative or had toxic effects [Keane et al. (1983) Neuropharmacology 22: 875-879].
Serious side effects that have been reported with anticonvulsant drugs, including deaths from hematological reactions, impaired mental and motor function, may limit clinical use, particularly in elderly people [Martindale: The Extra Pharmacopeia. 31
st
Edition. London: Pharmaceutical Press, (Editor Reynolds) 1996, pgs. 367-381]. Moreover, the results of several clinical trials with anticonvulsant drugs were disappointing and show conflicting results [McQuay et al. (1995) BMJ 311:1047-1052]. In particular, there is no evidence that anticonvulsants are effective for acute pain [Wiffen et al. (2000) The Cochrane Library, Issue 4, Oxford: Update Software].
Overall, it seems that the therapeutic effects of many of the existing analgesic agents are controversial and often inadequate. In addition, most of the currently available analgesic medicaments suffer from serious drawbacks which limit their use.
Clearly, there is an unmet clinical need for novel substances for effective treatment of various forms of pain, including acute and neuropathic pain.
SUMMARY OF THE INVENTION
The aim of the present invention is to provide methods for the treatment and/or prophylaxis of pain in mammals, in particular acute and neuropathic pain in humans.
Thus the present invention relates, in one aspect, to methods of treating or alleviating pain in mammals, comprising administering to a mammal suffering from pain, a pain-alleviating amount of a compound of the general formula (I) or (II) or pharmaceutically acceptable salts thereof.
The useful compounds according to the invention are of the general formula (I):
and pharmaceutically acceptable salts thereof, whe
Duvdevani Revital
Kozak Alexander
Younis Firas M.
Carr Deborah D.
D-Pharm Ltd.
Davidson Davidson & Kappel LLC
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