IP Library Granted Patent US 7,553,858
Granted Patent B2
US 7,553,858 · App. 11/002,762 · Granted Jun 30, 2009

Combination of flupirtine and tramadol

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Quick Facts
Patent No.
US 7,553,858
App. No.
11/002,762
Granted
Jun 30, 2009
Kind
B2
Abstract

The subject of the present invention is to provide a combination of two centrally acting analgesics, flupirtine and tramadol, or their respective pharmaceutically acceptable salts for the treament of pain.

Claims (21)

1. A method for the treatment of pain comprising administering effective amounts of flupirtine in combination with tramadol or their respective physiologically acceptable salts to a patient in need of such treatment, wherein the combination of flupirtine and tramadol intensifies their antinociceptive/analgesic activities.

2. The method according to claim 1 where the pain is caused by increased skeletal muscle tone.

3. The method according to claim 1 where the pain is caused by pain in cancer.

4. The method according to claim 1 for the treatment of rheumatic pain.

5. The method according to claim 1 where the pain is caused by painful musculosketal disorders with hypermyotonia and decreased motility.

6. The method according to claim 1 where the pain is caused by neuralgia and/or neuropathy.

7. The method according to claim 1 for the treatment of chronic or episodic or tension headache or migraine.

8. The method according to claim 1 for the treatment of post-surgical or post-traumatic pain and dental pain.

9. The method according to claim 1 where the pain is caused by lower spastic paraperesis syndrome or tetrapareses.

10. The method according to claim 1 where the pain is caused by biliary or renal colic.

11. A method for the treatment of pain comprising administering effective amounts of flupirtine in combination with tramadol or their respective physiologically acceptable salts in an oral, rectal, intravenous, transdermal or subcutaneous or intracutaneous form to a patient in need of such treatment, wherein the combination of flunirtine and tramadol intensifies their antinociceptive/analgesic activities.

12. The method according to claim 1 , wherein the daily dosage for tramadol is 50 to 400 mg/day and that the daily dosage of flupirtine is 100 to 800 mg/day.

13. The method according to claim 1 , wherein the daily dosage for tramadol is 100 to 400 mg/day and the daily dose of flupirtine is 200 to 400/mg day.

14. The method according to claim 4 , wherein the rheumatic pain is caused by arthrose and/or arthritis.

15. The method according to claim 5 , wherein the pain is caused by disk relapse, disk protrusion, inervertebral disk lesions, intervertebral chondrosis, osteochondrosis, cervical myelopathy, vertebral dysplasia, cervico-brachalgia, low bak syndrome, and/or ischio-lumbalgia.

16. The method according to claim 5 , wherein the pain results from spinal cord injuries, osteoporosis, rigidity and/or spasticity.

17. the method according to claim 6 , wherein the pain is myofascial pain.

18. The method according to claim 6 , wherein the pain is caused by trigeminal neuralgia and/or shingles neuralgia.

19. The method according to claim 8 , wherein the post-traumatic pain is caused by bone fracture.

20. The method according to claim 9 , wherein the pain is caused by lower paraspasmus, transversal myelitis, multiple sclerosis, hereditary spastic paraplegia inferior, Stuempel paraplegia, disturbances of the spinal blood circulation, and/or cerebral palsy with lower spastic paresis.

21. The method according to claim 1 , wherein the effective amount of flupirtine is sufficient to reduce emesis induced by the tramadol.

Assignments (2)
CHANGE OF NAME Recorded Jan 30, 2007
From: VIATRIS GMBH & CO. KG
To: MEDA PHARMA GMBH & CO. KG
Reel/Frame 018826/0219 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 7, 2005
From: SZELENYI, ISTVAN; MAUS, JOACHIN; CNOTA, PETER J.
To: VIATRIS GMBH & CO. KG
Reel/Frame 016033/0939 →