IP Library Granted Patent US 8,741,886
Granted Patent B2
US 8,741,886 · App. 13/706,907 · Granted Jun 3, 2014

Baclofen and acamprosate based therapy of neurological disorders

Inventors: Daniel Cohen (Le Vesinet, FR); Ilya Chumakov (Vaux le Penil, FR); Serguei Nabirochkin (Chatenay Malabry, FR); Emmanuel Vial (Paris, FR); Mickael Guedj (Paris, FR)
Assignee: Pharnext
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Quick Facts
Patent No.
US 8,741,886
App. No.
13/706,907
Granted
Jun 3, 2014
Kind
B2
Abstract

The present invention relates to combinations and methods for the treatment of neurological disorders related to glutamate excitotoxicity and Amyloid β toxicity. More specifically, the present invention relates to novel combinatorial therapies of Multiple Sclerosis, Alzheimer's disease, Alzheimer's disease related disorder, Amyotrophic Lateral Sclerosis, Parkinson's disease, Huntington's disease, neuropathic pain, alcoholic neuropathy, alcoholism or alcohol withdrawal, or spinal cord injury, based on Baclofen and Acamprosate combination.

Claims (31)

1. A method of treating Alzheimer's disease or a related disease selected from senile dementia of AD type (SDAT), mild cognitive impairment (MCI) and age-associated memory impairment (AAMI), comprising administering to a subject in need thereof a synergistic combination of baclofen and acamprosate, or pharmaceutically acceptable salts thereof, in an amount effective to treat said subject.

2. The method of claim 1 , wherein baclofen and acamprosate are mixed with a pharmaceutically acceptable carrier or excipient.

3. The method of claim 1 , wherein baclofen and acamprosate are formulated or administered together, separately or sequentially.

4. The method of claim 1 , wherein baclofen and acamprosate are administered repeatedly to the subject.

5. The method of claim 1 , wherein the synergistic combination of baclofen and acamprosate has a ratio of Acamprosate/Baclofen (W:W) between 0.1 and 1000.

6. The method of claim 1 , wherein baclofen is administered at a dose of between 0.01 and 150 mg/day.

7. The method of claim 1 , wherein acamprosate is administered at a dose of less than 400 mg/day.

8. The method of claim 1 , wherein a calcium salt of acamprosate is used.

9. The method of claim 1 , comprising administering to the subject:

baclofen and acamprosate,

baclofen and acamprosate and diethylcarbamazine,

baclofen and acamprosate and cinacalcet,

baclofen and acamprosate and sulfisoxazole,

baclofen and acamprosate and torasemide,

baclofen and acamprosate and ifenprodil,

baclofen and acamprosate and mexiletine,

baclofen and acamprosate and eplerenone,

baclofen and acamprosate and levosimendan,

baclofen and acamprosate and terbinafine, or

baclofen and acamprosate and leflunomide.

10. The method of claim 1 , comprising administering to a subject a composition comprising:

baclofen, acamprosate and donepezil,

baclofen, acamprosate and rivastigmine, or

baclofen, acamprosate and memantine.

11. The method of claim 1 , comprising administering to the subject baclofen and acamprosate as the only active agents.

12. A method for improving cognitive functions in a subject suffering from, predisposed to, or suspected to suffer from Alzheimer's disease, the method comprising administering to said subject a synergistic combination of baclofen and acamprosate, or pharmaceutically acceptable salts thereof in an amount effective to treat said subject.

13. A method for improving memory in a subject suffering from, predisposed to, or suspected to suffer from Alzheimer's disease, the method comprising administering to said subject a synergistic combination of baclofen and acamprosate, or pharmaceutically acceptable salts thereof in an amount effective to treat said subject.

14. The method of claim 1 , wherein baclofen and acamprosate act synergistically in protecting neuronal or endothelial cells from Aβ toxicity in vitro.

15. The method of claim 1 , wherein the subject is a human subject.

16. The method of claim 1 , wherein said subject is a human subject having Alzheimer's disease.

17. The method of claim 1 , said method comprising administering 0.01 to 150 mg/day of baclofen, or pharmaceutically acceptable salts thereof, and less than 400 mg/day of acamprosate, or pharmaceutically acceptable salts thereof, as the synergistic combination of baclofen and acamprosate to said subject.

Assignments (5)
RELEASE OF SECURITY INTEREST Recorded Sep 13, 2022
From: IPF MANAGEMENT S.A., AS BONDHOLDERS' REPRESENTATIVE
To: PHARNEXT S.A.
Reel/Frame 061081/0098 →
RELEASE OF SECURITY INTEREST Recorded Sep 18, 2018
From: KREOS CAPITAL IV (UK) LIMITED
To: PHARNEXT
Reel/Frame 046895/0584 →
SECURITY INTEREST Recorded Sep 4, 2018
From: PHARNEXT S.A.
To: IPF MANAGEMENT S.A., AS BONDHOLDERS' REPRESENTATIVE
Reel/Frame 046775/0111 →
SECURITY INTEREST Recorded Apr 12, 2016
From: PHARNEXT
To: KREOS CAPITAL IV (UK) LIMITED
Reel/Frame 038251/0878 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Dec 7, 2012
From: COHEN, DANIEL; CHUMAKOV, ILYA; NABIROCHKIN, SERGUEI; VIAL, EMMANUEL; GUEDJ, MICKAEL
To: PHARNEXT
Reel/Frame 029424/0568 →
Priority Claims (2)
EP 11305217 · Mar 1, 2011 · regional
EP 11305687 · Jun 6, 2011 · regional
Continuity (4)
Continuation PCTEP2012053570 · Mar 1, 2012
Provisional Application 61468658 · Mar 29, 2011
Provisional Application 61493606 · Jun 6, 2011
Related Publication 20130090307A1 · Apr 11, 2013