US2015306109A1PendingUtilityA1
Compositions Comprising Nicotinic Agonists and Methods of Using Same
Est. expiryNov 26, 2027(~1.3 yrs left)· nominal 20-yr term from priority
Inventors:Eliahu Heldman
A61P 43/00A61P 25/16A61P 25/28A61P 25/00A61P 25/34A61P 25/18A61P 25/14A61P 25/24A61P 25/32A61P 25/22A61P 25/36A61K 31/4439A61K 31/4406A61K 9/0053A61K 31/465A61K 31/27A61K 31/167A61K 31/136A61K 31/55A61K 9/0014
63
PatentIndex Score
0
Cited by
0
References
0
Claims
Abstract
The disclosure is directed at least in part to compositions and methods comprising nicotinic agonists for treating e.g., nervous system disorders, in particular, to combination therapies that include a nicotinic agonist (for example, nicotine) and a nicotinic acetylcholine receptor desensitization inhibitor (for example, opipramol).
Claims
exact text as granted — not AI-modified1 - 3 . (canceled)
4 . A method of treating anxiety or depression, comprising co-administering to a patient in need thereof a therapeutically effective amount of nicotine, or a pharmaceutically acceptable salt or N-oxide thereof, and opipramol, or a pharmaceutically acceptable salt or ester thereof.
5 - 7 . (canceled)
8 . The method of claim 4 , wherein administration of a nicotinic agonist after said co-administration prolongs the duration of the nicotinic agonist effect by about a factor of two as compared to administering to the patient the nicotinic agonist alone.
9 . (canceled)
10 . The method of claim 4 , wherein said opipramol reduces the desensitization of nicotinic acetylcholine receptors to said nicotine for at least about 12 hours.
11 - 12 . (canceled)
13 . The method of claim 4 , wherein said nicotine and said opipramol are administered together in the same dosage form.
14 . The method of claim 4 , wherein said nicotine and said opipramol are administered in separate dosage forms.
15 - 17 . (canceled)
18 . The method of claim 4 , wherein said nicotine and said opipramol, are each administered via a formulation chosen from: oral, parenteral, mucosal, inhalation and transdermal formulations, or a combination thereof.
19 . (canceled)
20 . The method of claim 4 , wherein the nicotinic agonist is administered transdermally.
21 - 25 . (canceled)
26 . The method of claim 4 , wherein said nicotine and said opipramol are administered in one transdermal patch.
27 - 34 . (canceled)
35 . The method of claim 4 , wherein about 5 mg/day to about 21 mg/day of the nicotine is administered.
36 - 46 . (canceled)
47 . The method of claim 4 , wherein said nicotine and said opipramol are present in a weight ratio of nicotine:opipramol of about 1:2 to about 1:100.
48 . The method of claim 4 , wherein said nicotine and said opipramol are present in a weight ratio of nicotine:opipramol of about 1:5 to about 1:20.
49 - 66 . (canceled)
67 . The method of claim 4 , wherein said nicotine and said opipramol are present in a weight ratio of nicotine:opipramol of about 1:1.
68 . A method of treating anxiety, comprising co-administering to a patient in need thereof a therapeutically effective amount of nicotine, or a pharmaceutically acceptable salt or N-oxide thereof, and opipramol, or a pharmaceutically acceptable salt or ester thereof.
69 . A method of treating depression, comprising co-administering to a patient in need thereof a therapeutically effective amount of nicotine, or a pharmaceutically acceptable salt or N-oxide thereof, and opipramol, or a pharmaceutically acceptable salt or ester thereof.Join the waitlist — get patent alerts
Track US2015306109A1 — get alerts on status changes and closely related new filings.
We store only your email — no account needed. See our privacy policy.