Method of biochemical treatment of persistent pain

• US 20050152905A1
• Filed: 02/16/2005
• Published: 07/14/2005
• Est. Priority Date: 08/22/2002
• Status: Abandoned Application

• Current Assignee: Osemwota Sota Omoigui
• Original Assignee: Osemwota Sota Omoigui
• Inventors: Omoigui, Osemwota Sota
• Application Number:
  US11/058,371
• Publication Number:
  US 20050152905A1
• Time in Patent Office: Days
• US Class Current: 424/145.100
• CPC Class Codes: A61K 2039/505 comprising antibodies
• CPC Class Codes: A61K 31/00 Medicinal preparations containing organic active ingredients
• CPC Class Codes: A61K 38/177 Receptors; Cell surface antigens; Cell surface determinants
• CPC Class Codes: A61K 38/1793 for cytokines; for lymphokines; for interferons
• CPC Class Codes: A61K 38/20 Interleukins [IL]
• CPC Class Codes: A61K 38/4886 Metalloendopeptidases (3.4.24), e.g. collagenase
• CPC Class Codes: A61K 38/4893 Botulinum neurotoxin (3.4.24.69)
• CPC Class Codes: C07K 16/241 Tumor Necrosis Factors

Abstract

This invention relates to a method for the biochemical treatment of persistent pain disorders by inhibiting the biochemical mediators of inflammation in a subject comprising administering to said subject any one of several combinations of components that are inhibitors of biochemical mediators of inflammation. Said process for biochemical treatment of persistent pain disorders is based on Sota Omoigui'"'"'s Law, which states: ‘The origin of all pain is inflammation and the inflammatory response’. Sota Omoigui'"'"'s Law of Pain unifies all pain syndromes as sharing a common origin of inflammation and the inflammatory response. The various biochemical mediators of inflammation are present in differing amounts in all pain syndromes and are responsible for the pain experience. Classification and treatment of pain syndromes should depend on the complex inflammatory profile. A variety of mediators are generated by tissue injury and inflammation. These include substances produced by damaged tissue, substances of vascular origin as well as substances released by nerve fibers themselves, sympathetic fibers and various immune cells. Biochemical mediators of inflammation that are targeted for inhibition include but are not limited to: prostaglandin, nitric oxide, tumor necrosis factor alpha, interleukin 1-alpha, interleukin 1-beta, interleukin-4, Interleukin-6 and interleukin-8, histamine and serotonin, substance P, Matrix Metallo-Proteinase, calcitonin gene-related peptide, vasoactive intestinal peptide as well as the potent inflammatory mediator peptide proteins neurokinin A, bradykinin, kallidin and T-kinin.

Claims

1. A method of the biochemical treatment of persistent pain disorders in a human or other animal subject, in accordance with Sota Omoigui'"'"'s Law of Pain, which states that, the origin of all pain is inflammation and the inflammatory response. Said method comprises administering, to said subject, any one of the following combinations of components that are inhibitors of biochemical mediators of inflammation:

I. A and C

II. A and E

III. A, B, C and D

IV. A, B, C and E

V. A, B, D and E

VI. A, B, C, D and E

Wherein

A is a Prostaglandin inhibitor selected from the group consisting of corticosteroids, botulinum toxin, acetaminophen;

ibuprofen;

flurbiprofen;

ketoprofen;

naproxen;

oxaprozin;

etodolac;

indomethacin;

ketorolac;

nabumetone;

piroxicam;

celecoxib;

rofecoxib;

meloxicam;

JTE-522;

L-745, 337; and

NS398;

or a pharmaceutically acceptable salt thereof.

B. is a modulator of neuronal transmission and an inhibitor of neuronal neuropeptide (substance p, glutamate, calcitonin gene related peptide, bradykinin, nitric oxide) release, selected from the group including of opioid analgesics, Ca(+) channel blockers, Na(+) channel blocKers, k(+) channel blockers, oxcarbazepine, zonisamide, lamotrigine, gabapentin, valproic acid, topiramate, carbamazepine, clonazepam, divalproex sodium, valproate sodium, an ester thereof, a pharmaceutically acceptable salt thereof, a hydrate thereof;

C. is an interleukin-1 (IL-1) inhibitor selected from the group including of interleukin 1 receptor antagonist (IL-1 RA), interleukin 1 receptor type II (IL-1R type II), monoclonal antibodies to interleukin 1 (including both chimeric and fully humanized forms), soluble receptors to interleukin 1, soluble receptors to interleukin 1 fused to an F.sub.c immunoglobulin fragment, bisphosphonates such as Pamidronate, Etidronate, Clodronate, Alendronate, phosphonic acid derivatives, an ester thereof, a pharmaceutically acceptable salt thereof, a hydrate thereof.

D. is an interleukin-6 (IL-6) inhibitor, selected from the group comprising monoclonal antibodies to IL-6, bisphosphonates such as Pamidronate, Etidronate, Clodronate, Alendronate, phosphonic acid derivatives, an ester thereof, a pharmaceutically acceptable salt thereof, a hydrate thereof

E. is a Tumor Necrosis Factor-Alpha (TNF-alpha) inhibitor selected from the group including of infliximab, adalimumab, etanercept, pegylated soluble TNF receptor Type I (PEGsTNF-R11), CDP571 (a humanized monoclonal anti-TNF-alpha antibody), D2E7 (a human anti-TNF mAb), Thalidomide based compounds, Tetracyclines, Pentoxifylline and Phosphodiesterase inhibitors.

said components being administered simultaneously or separately, in amounts which in combination have the effect of ameliorating the persistent pain disorder.

2. The method of claim 1, wherein;

a) said persistent pain disorder is musculoskeletal pain.

b) a therapeutically effective amount of said combinations of inhibitors of biochemical mediators of inflammation is administered subcutaneously, intramuscularly, intravenously, orally, rectally, by intra-articular, epidural or intrathecal injection.

3. The method of claim 1, wherein;

a) said persistent pain disorder is joint pain.

b) a therapeutically effective amount of said combinations of inhibitors of biochemical mediators of inflammation is administered subcutaneously, intramuscularly, intravenously, orally, rectally, by intra-articular, epidural or intrathecal injection.

4. The method of claim 1, wherein;

a) said persistent pain disorder is bone pain.

b) a therapeutically effective amount of said combinations of inhibitors of biochemical mediators of inflammation is administered subcutaneously, intramuscularly, intravenously, orally, rectally, by intra-articular, epidural or intrathecal injection.

5. The method of claim 1, wherein;

a) said persistent pain disorder is osteoarthritis or any other type of arthritis.

b) a therapeutically effective amount of said combinations of inhibitors of biochemical mediators of inflammation is administered subcutaneously, intramuscularly, intravenously, orally, rectally, by intra-articular, epidural or intrathecal injection.

6. The method of claim 1, wherein;

a) said persistent pain disorder is ligament or meniscus tear.

b) a therapeutically effective amount of said combinations of inhibitors of biochemical mediators of inflammation is administered subcutaneously, intramuscularly, intravenously, orally, rectally, by intra-articular, epidural or intrathecal injection.

7. The method of claim 1, wherein;

a) said persistent pain disorder is back or neck pain arising from injury to the nerve, muscle, joint, ligament or disk.

b) a therapeutically effective amount of said combinations of inhibitors of biochemical mediators of inflammation is administered subcutaneously, intramuscularly, intravenously, orally, rectally, by intra-articular, epidural or intrathecal injection.

8. The method of claim 1, wherein;

a) said persistent pain disorder is nerve pain including neurogenic inflammation, neuralgia, carpal tunnel syndrome, post herpetic neuralgia, phantom limb pain, vulvodynia.

b) a therapeutically effective amount of said combinations of inhibitors of biochemical mediators of inflammation is administered subcutaneously, intramuscularly, intravenously, orally, rectally, by intra-articular, epidural or intrathecal injection.

9. The method of claim 1, wherein;

a) said persistent pain disorder is neuropathic pain syndrome including neuralgia or nerve pain, carpal tunnel syndrome, post herpetic neuralgia, phantom limb pain, vulvodynia.

b) a therapeutically effective amount of said combinations of inhibitors of biochemical mediators of inflammation is administered subcutaneously, intramuscularly, intravenously, orally, rectally, by intra-articular, epidural or intrathecal injection.

10. The method of claim 1, wherein;

a) said persistent pain disorder is chronic regional pain syndrome also known as reflex sympathetic dystrophy.

b) a therapeutically effective amount of said combinations of inhibitors of biochemical mediators of inflammation is administered subcutaneously, intramuscularly, intravenously, orally, rectally, by intra-articular, epidural or intrathecal injection.

11. The method of claim 1, wherein;

a) said persistent pain disorder is fibromyalgia.

b) a therapeutically effective amount of said combinations of inhibitors of biochemical mediators of inflammation is administered subcutaneously, intramuscularly, intravenously, orally, rectally, by intra-articular, epidural or intrathecal injection.

12. The method of claim 1, wherein;

a) said persistent pain disorder is muscle pain

b) a therapeutically effective amount of said combinations of inhibitors of biochemical mediators of inflammation is administered subcutaneously, intramuscularly, intravenously, orally, rectally, by intra-articular, epidural or intrathecal injection.

13. The method of claim 1, wherein;

a) said persistent pain disorder is osteoporosis pain

b) a therapeutically effective amount of said combinations of inhibitors of biochemical mediators of inflammation is administered subcutaneously, intramuscularly, intravenously, orally, rectally, by intra-articular, epidural or intrathecal injection.

14. The method of claim 1, wherein;

a) said persistent pain disorder is bursitis including rotator cuff bursitis.

b) a therapeutically effective amount of said combinations of inhibitors of biochemical mediators of inflammation is administered subcutaneously, intramuscularly, intravenously, orally, rectally, by intra-articular, epidural or intrathecal injection.

15. The method of claim 1, wherein;

a) said persistent pain disorder is tendonitis.

b) a therapeutically effective amount of said combinations of inhibitors of biochemical mediators of inflammation is administered subcutaneously, intramuscularly, intravenously, orally, rectally, by intra-articular, epidural or intrathecal injection.

16. The method of claim 1, wherein;

a) said persistent pain disorder is soft tissue pain.

b) a therapeutically effective amount of said combinations of inhibitors of biochemical mediators of inflammation is administered subcutaneously, intramuscularly, intravenously, orally, rectally, by intra-articular, epidural or intrathecal injection.

17. The method of claim 1, wherein;

a) said persistent pain disorder is migraine.

b) a therapeutically effective amount of said combinations of inhibitors of biochemical mediators of inflammation is administered subcutaneously, intramuscularly, intravenously, orally, rectally, by intra-articular, epidural or intrathecal injection.

18. The method of claim 1, wherein;

a) said persistent pain disorder is interstitial cystitis.

b) a therapeutically effective amount of said combinations of inhibitors of biochemical mediators of inflammation is administered subcutaneously, intramuscularly, intravenously, orally, rectally, by intra-articular, epidural or intrathecal injection.

19. A method of treating bone density disorders in a human or other animal subject, in accordance with Sota Omoigui'"'"'s Law of Pain, which states that, the origin of all pain is inflammation and the inflammatory response and the primary origin of osteoporosis is inflammation and the inflammatory response. Said method comprises administering, to said subject, any one of the following combinations of components that are inhibitors of biochemical mediators of inflammation:

I. A and B

II. A, B and C

Wherein

A is an interleukin-1 (IL-1) inhibitor selected from the group including of interleukin 1 receptor antagonist (IL-1 RA), interleukin 1 receptor type II (IL-1R type II), monoclonal antibodies to interleukin 1 (including both chimeric and fully humanized forms), soluble receptors to interleukin 1, soluble receptors to interleukin 1 fused to an F.sub.c immunoglobulin fragment, bisphosphonates such as Pamidronate, Etidronate, Clodronate, Alendronate, phosphonic acid derivatives, an ester thereof, a pharmaceutically acceptable salt thereof, a hydrate thereof.

B is an interleukin-6 (IL-6) inhibitor, selected from the group comprising monoclonal antibodies to IL-6, bisphosphonates such as Pamidronate, Etidronate, Clodronate, Alendronate, phosphonic acid derivatives, an ester thereof, a pharmaceutically acceptable salt thereof, a hydrate thereof, HMG-CoA reductase inhibitors such as lovastatin, simvastatin, pravastatin, fluvastatin, atorvastatin, rivastatin, red yeast rice, red yeast grain, red yeast powder and other statins or a pharmaceutically acceptable salt thereof.

C is a Tumor Necrosis Factor-Alpha (TNF-alpha) inhibitor selected from the group including of infliximab, adalimumab, etanercept, pegylated soluble TNF receptor Type I (PEGsTNF-R1), CDP571 (a humanized monoclonal anti-TNF-alpha antibody), D2E7 (a human anti-TNF mAb), Thalidomide based compounds, Tetracyclines, Pentoxifylline and Phosphodiesterase inhibitors.

said components being administered simultaneously or separately, in amounts which in combination have the effect of ameliorating the bone density disorder.

20. The method of claim 19, wherein;

a) said persistent bone density disorder is osteoporosis

b) a therapeutically effective amount of said combinations of inhibitors of biochemical mediators of inflammation is administered subcutaneously, intramuscularly, intravenously, orally, rectally, by intra-articular, epidural or intrathecal injection.

21. The method of claim 19, wherein;

a) said persistent bone density disorder is osteopenia

b) a therapeutically effective amount of said combinations of inhibitors of biochemical mediators of inflammation is administered subcutaneously, intramuscularly, intravenously, orally, rectally, by intra-articular, epidural or intrathecal injection.

22. The method of claim 19, wherein;

a) said persistent bone density disorder is inflammatory bone pain

b) a therapeutically effective amount of said combinations of inhibitors of biochemical mediators of inflammation is administered subcutaneously, intramuscularly, intravenously, orally, rectally, by intra-articular, epidural or intrathecal injection.