52 results about "Peripheral neuropathic pain" patented technology

The present invention relates to the use of tarenflurbil and / or a pharmaceutically tolerable salt or derivative thereof in enantiomerically-pure and / or essentially enantiomerically-pure form or a form that is enriched with respect to flurbiprofen racemate and / or a racemate of said salt or derivative, for the production of a drug for the treatment of pain-associated neuropathy, pain-associated neuropathy that is simultaneously accompanied by states of nociceptive pain, peripheral and / or predominantly peripheral neuropathic pain or central and / or predominantly central neuropathic pain.

This invention describes a topical delivery mechanism that contains a mixture of cetylated fatty esters that act as transdermal carriers of desired therapeutic molecules. The proposed cetyl fatty ester penetrant-complex (Base CFEP-complex) contains specific cetyl fatty esters, polar solvents, a carrier base (gel, cream, lotion, patch or stick gel), antioxidants and the desired pharmaceutical, cosmetic or antigenic response eliciting molecules that are efficaciously delivered by selectively varying component ratios in the complex. The invention proposes the use of transdermal delivery of medications such as those used in treatment of urinary incontinence, testosterone deficiency, arthritic and joint pain and other pains such as pain in the neck, lower back, back, knees, headaches, and other types of inflammatory pains, peripheral neuropathic pain, pain associated with repetitive strain injuries such as myofacial pain, rapid treatment of epileptic seizures, soluble antigens in the immuno-therapeutic treatment of allergies, actives in the treatment of foot cracks and elbow cracks, actives in the treatment of facial and other wrinkles in the form of anti-aging creams and gels and other topically delivered therapies.

The present invention relates to the use of a combination of cannabinoids in the treatment of neuropathic pain, in particular peripheral neuropathic pain. A combination of cannabidiol (CBD) and delta-9-tetrahydrocannabinol (THC) may be used, wherein the ratio of CBD:THC by weight is between 10:1 and 1:10.

Use of 1-phenyl-3-dimethylaminopropane compounds for the production of medicaments for treating neuropathic pain, preferably polyneuropathic pain, also preferably diabetic neuropathic pain, more preferably diabetic peripheral neuropathic pain, and furthermore preferably for treating diabetic peripheral neuropathy.

This invention describes a topical delivery mechanism that contains a mixture of cetylated fatty esters that act as transdermal carriers of desired therapeutic molecules. The proposed cetyl fatty ester penetrant-complex (Base CFEP-complex) contains specific cetyl fatty esters, polar solvents, a carrier base (gel, cream, lotion, patch or stick gel), antioxidants and the desired pharmaceutical, cosmetic or antigenic response eliciting molecules that are efficaciously delivered by selectively varying component ratios in the complex. The invention proposes the use of transdermal delivery of medications such as those used in treatment of urinary incontinence, testosterone deficiency, arthritic and joint pain and other pains such as pain in the neck, lower back, back, knees, headaches, and other types of inflammatory pains, peripheral neuropathic pain, pain associated with repetitive strain injuries such as myofacial pain, rapid treatment of epileptic seizures, soluble antigens in the immuno-therapeutic treatment of allergies, actives in the treatment of foot cracks and elbow cracks, actives in the treatment of facial and other wrinkles in the form of anti-aging creams and gels and other topically delivered therapies.

The invention provides a pharmaceutical composition of duloxetine or its pharmaceutically equivalent derivatives like salts, isomers, complexes, polymorphs, hydrates or esters thereof and at least one buffering agent. The duloxetine or its pharmaceutically equivalent derivative is present from about 2 mg to approximately 200 mg; and the buffering agent is present in an amount of approximately 0.1 mEq to approximately 2.5 mEq per mg of duloxetine. Also provided is a method for treating of major depressive disorder and or diabetic peripheral neuropathic pain comprising administering to a mammal in need of such treatment a therapeutically effective amount of a composition.

The invention provides for the first time an oral liquid composition of duloxetine or its pharmaceutically equivalent derivatives like salts, isomers, complexes, polymorphs, hydrates or esters thereof. The duloxetine or its pharmaceutically equivalent derivative is present from about 2 mg to approximately 200 mg; and a buffering agent was used to stabilize the acid sensitive duloxetine. The composition has duloxetine from about 0.1 meq to about 2.5 mEq per mg of duloxetine. The invention further discloses an oral liquid composition of duloxetine or its pharmaceutically equivalent derivative wherein the degradation product 1-Naphthol is less than 0.01%. Also provided is a method for treating of major depressive disorder and or diabetic peripheral neuropathic pain comprising administering to a mammal in need of such treatment a therapeutically effective amount of a composition.

The present invention concerns the novel use of compounds of the Formula I: for treating allodynia as major and unique pain symptom independent of the nature of an underlying disease, but that is often related to neuropathic pain or other different types of chronic or phantom pain.

The invention refers to the use of a sigma ligand, particularly a sigma ligand of formulae (I), (II) or (III) to prevent and / or treat acute and chronic pain developed as a consequence of surgery, especially superficial and / or deep pain secondary to surgical tissue injury, and peripheral neuropathic pain, neuralgia, allodynia, causalgia, hyperalgesia, hyperesthesia, hyperpathia, neuritis or neuropathy secondary to surgical procedure.

Use of 1-phenyl-3-dimethylaminopropane compounds for the production of medicaments for treating neuropathic pain, preferably polyneuropathic pain, also preferably diabetic neuropathic pain, more preferably diabetic peripheral neuropathic pain, and furthermore preferably for treating diabetic peripheral neuropathy.

The invention provides for the first time an oral liquid composition of duloxetine or its pharmaceutically equivalent derivatives like salts, isomers, complexes, polymorphs, hydrates or esters thereof. The duloxetine or its pharmaceutically equivalent derivative is present from about 2 mg to approximately 200 mg; and a buffering agent was used to stabilize the acid sensitive duloxetine. The composition has duloxetine from about 0.1 meq to about 2.5 mEq per mg of duloxetine. The invention further discloses an oral liquid composition of duloxetine or its pharmaceutically equivalent derivative wherein the degradation product 1-Naphthol is less than 0.01%. Also provided is a method for treating of major depressive disorder and or diabetic peripheral neuropathic pain comprising administering to a mammal in need of such treatment a therapeutically effective amount of a composition.

A medicament effective for prophylactic and / or therapeutic treatment of a peripheral neuropathic pain such as allodynia caused by a treatment with an anticancer agent, which comprises thrombomodulin as an active ingredient.

The invention provides a method of treating spinal cord injury pain or peripheral neuropathic pain in a mammal comprising administering to a mammal a vector comprising a nucleotide sequence encoding a glutamic acid decarboxylase (GAD) protein in an amount effective to treat spinal cord injury pain or peripheral neuropathic pain.

A method of treating peripheral neuropathic pain in humans resulting from a peripheral nerve injury and for treating muscle spasm in humans resulting from a peripheral nerve injury comprises applying a therapeutically effective amount of a drug selected from the group consisting of a dopamine agonist, a skeletal muscle relaxant, and a combination thereof topically to the site of the injury.

The invention refers to a combination comprising a sigma ligand of formula (I) and an opioid or opiate for use in the prevention and / or treatment of pain developed as a consequence of surgery, especially peripheral neuropathic pain, allodynia, causalgia, hyperalgesia, hyperesthesia, hyperpathia, neuralgia, neuritis or neuropathy. The invention also refers to the sigma ligands of formula (I) for use in potentiating the analgesic effect of an opioid or opiate and / or for decreasing the dependency induced thereby when said opioid or opiate is used in the prevention and / or treatment of pain developed as a consequence of surgery.

A plasma radiofrequency ablation and puncture trocar combination device. The invention relates to the field of medical devices. It includes an external puncture trocar and a built-in radio frequency puncture needle. The external puncture trocar is composed of a needle point, a needle body and a needle wing. The needle point and the needle body are coated with Teflon. The built-in radio frequency puncture needle Consists of a needle tip, a needle body, a needle seat and a needle core. There is no Teflon coating on the outside of the needle tip, and the length is 2mm. The outside of the needle body has a Teflon coating. The tip of the needle tip is 5 mm, and the inner diameter of the external puncture trocar corresponds to the outer diameter of the built-in radio frequency puncture needle, and the external puncture trocar and the built-in radio frequency puncture needle are detachable structures. The invention has the advantages of simple structure, low cost and convenient use, and provides technical convenience for patients with peripheral neuralgia to implement low-temperature plasma radiofrequency ablation to establish a working channel.

The invention belongs to the field of traditional Chinese medicine, and particularly relates to a traditional Chinese medicine composition for treating diabetic peripheral neuropathic pain and a preparation method thereof. The traditional Chinese medicine composition is prepared from Semen Coicis, Astragalus root, radix codonopsitis, resina draconis, radix angelicae pubescentis, hemlock parsley, futokadsura stem and liquorice. The traditional Chinese medicine composition provided by the invention has the advantages of obvious treatment effect on diabetic peripheral neuropathic pain, low recurrence rate and no adverse reaction.

The use of vitamin D3 for the manufacture of a medicament for the transdermal treatment of neurogenic inflammation and neuropathic pain (including peripheral neuropathic pain); also a method for the relief of neurogenic inflammation and neuropathic pain using this medicament.

Pain, for example, neuropathic pain such as peripheral neuropathic pain, may be treated or alleviated by administering to a subject an effective amount of one or more caspase inhibitors. Activator and effector caspases, defining components of programmed cell death (PCD, apoptosis) signaling pathways, have been found to also contribute to pain-related behavior in animals with small-fiber peripheral neuropathies. The death receptor ligand, tumor necrosis factor alpha (TNFα) and its downstream second messenger, ceramide, also produce pain-related behavior via this mechanism.

The invention belongs to the field of chemical drugs and in particular relates to a transdermal absorption preparation for treating diabetic peripheral neuropathic pain. The transdermal absorption preparation is prepared from gamma-aminobutyric acid analogue-like analgesic and small-molecule tricarbonyl nitrogen-containing compounds, and pharmaceutical excipients of the preparation include Carbomer 940, glycerin, Tween-80, triethanolamine, laurocapram and distilled water. Due to topical drug delivery, the transdermal absorption preparation has an obvious effect of relieving the diabetic peripheral neuropathic pain. Moreover, the dose of the gamma-aminobutyric acid analogue-like analgesic can be reduced.

The present invention pertains to a drug for the treatment and / or prevention of pain, more specifically to a medicinal preparation for external use to treat and / or prevent peripheral neuropathic pain, the medicinal preparation containing as an active ingredient N2-{[1-ethyl-6-(4-methylphenoxy)-1H-benzimidazol-2-yl]methyl}-L-alaninamide.

The invention discloses a traditional Chinese medicine preparation for treating diabetic peripheral neuropathic pain and belongs to the technical field of traditional Chinese medicine. The preparation is prepared from, by weight, 0.5 part of cassia twigs, 0.2 part of radix angelicae, 0.35 part of Chinese mosla herb, 1.3 parts of fructus xanthii, 1.15 parts of peach twigs, 0.55 part of drynaria total flavonoids, 2 parts of schefflera kwangsiensis, 0.35 part of multiflower knotweed vines, 0.05 part of pearl powder, 0.4 part of semen ziziphi spinosae, 1.2 parts of fructus choerospondiatis, 1.25 parts of semen platycladi, 0.3 part of cinnamon, 0.25 part of clove, 0.015 part of fennel, 0.035 part of illicium verum, 0.5 part of prunus mume, 0.45 part of semen litchi, 0.15 part of tangerine seeds and 3 parts of auxiliary materials. The invention further provides a preparation method of the preparation. The traditional Chinese medicine is stable and controllable, and has a remarkable effect on treatment of peripheral neuropathic pain symptoms of diabetic patients. Clinical application verifies that symptom treatment side effects are few, the preparation is soft, harmless and free of addiction, obvious adverse effects do not occur, and the clinical total effective rate of the Chinese medicine reaches 86.7%.

The invention discloses an application of CDN1163 in preparation of a medicine for relieving or treating neuropathic pain, and the CDN1163 can act on neuropathic pain including one or more of central nervous pain and peripheral neuropathic pain, improves mechanical pain sensitivity and heat pain sensitivity caused by chronic sciatic nerve compression injury of rats, improves meuron shrinkage and astrocyte activation of lumbar intervertebral foramen 5 dorsal root ganglion, inhibits neuron excitability increase of lumbar intervertebral foramen 4-6 dorsal root ganglions, effectively relieves neuropathic pain symptoms, can remarkably reverse mechanical hyperalgesia and thermal hyperalgesia through repeated injection; no tolerance sign exists, after the medicine is stopped, the treatment effect can be maintained, and the CDN1163 is applied to preparation of medicines for relieving or treating neuropathic pain which is long in lasting time and difficult to treat.

The present disclosure provides a method for the treatment of a neuropathic pain including a central neuropathic pain or a peripheral neuropathic pain in a subject comprising the administration of antibodies that specifically bind to human FAM19A5 and compositions comprising such antibodies. The present disclosure also provides methods for treating a neuropathic pain including a symptom of neuropathic pain, and / or an underlining cause of a neuropathic pain, by administering an antibody that specifically binds to human FAM19A5. In a specific aspect, the method comprises administering antibodies specifically bind to human FAM19A5, e.g., binds to soluble human FAM19A5 with a KD of 10 nM or less, or binds to membrane bound human FAM19A5 with a KD of 10 nM or less, or both, as measured by a method known in the art, e.g., ELISA.

The present invention provides method and compositions for the treatment of peripheral neuropathic pain by administering to a patient a therapeutically effective amount of a buprenorphine dimer compound, wherein the two buprenorphine portions are linked via an ethylene spacer, and wherein the spacer is bonded to the two opioid molecules via an ether bond. Preferably, the active agent is provided in the form of an injectable depot.

The invention refers to the use of a sigma ligand, particularly a sigma ligand of formulae (I), (II) or (III) to prevent and / or treat acute and chronic pain developed as a consequence of surgery, especially superficial and / or deep pain secondary to surgical tissue injury, and peripheral neuropathic pain, neuralgia, allodynia, causalgia, hyperalgesia, hyperesthesia, hyperpathia, neuritis or neuropathy secondary to surgical procedure.

The present disclosure relates to pharmaceutical compositions containing phenytoin or phenytoin sodium for use in topical pain relief. Use of the pharmaceutical composition of the disclosure reduces peripheral neuropathic pain. The topical pharmaceutical compositions of the disclosure containing phenytoin or phenytoin sodium, surprisingly reduce peripheral neuropathic pain considerably, especially and preferably in the conditions, characterized by a low to moderate grade of peripheral neurogenic inflammation, such as small fiber neuropathy, diabetic neuropathy, chronic idiopathic axonal polyneuropathy, post-herpetic neuralgia, trigeminus neuralgia, chemotherapy induced polyneuropathy, traumatic neuropathies, compression neuropathies, and infectious neuropathies in remission, according to the disclosure.

The present invention concerns methods and compositions that employ peptides that target dorsal root ganglion (DRG) neurons. In particular, the peptides are used to target therapeutic agents, such as proteins, liposomes, or viral particles comprising therapeutic polynucleotides, to one or more peripheral neuropathies or neuropathic pain, for example. In particular cases, the peripheral neuropathies or neuropathic pain is caused directly or indirectly by DRG neuronopathy.

The invention discloses a tetrodotoxin compound preparation which comprises the following components: tetrodotoxin, lidocaine, puerarin and an excipient. The invention also discloses use of the tetrodotoxin compound preparation in the preparation of a medicament for treating neuropathic pain, wherein the neuropathic pain is diabetic peripheral neuropathic pain or neuropathic injury pain. The novel tetrodotoxin compound preparation provided by the invention is used for treating diabetic peripheral neuropathic pain and neuropathic injury pain, and has advantages of small toxic side effect, good analgesic effect and the like.