IP Library Granted Patent US 12,090,140
Granted Patent B2
US 12,090,140 · App. 18/526,686 · Granted Sep 17, 2024

Non-sedating dexmedetomidine treatment regimens

Inventors: Vasukumar Kakumanu (New Haven, CT); David Christian Hanley (New Haven, CT); Frank Yocca (New Haven, CT); Chetan Dalpatbhai Lathia (New Haven, CT); Lavanya Rajachandran (New Haven, CT); Robert Risinger (New Haven, CT)
Assignee: BioXcel Therapeutics, Inc.
A61K31/4174A61K9/006A61K47/38A61P25/18A61P25/20
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Quick Facts
Patent No.
US 12,090,140
App. No.
18/526,686
Granted
Sep 17, 2024
Kind
B2
Abstract

Disclosed herein are methods of administering relatively high doses of dexmedetomidine or a pharmaceutically acceptable salt thereof to a human subject, without also inducing significant sedation. The disclosed methods are particularly suitable for the treatment of agitation, especially when associated with neurodegenerative and/or neuropsychiatric diseases such as schizophrenia, bipolar illness such as bipolar disorder or mania, dementia, depression, or delirium.

Claims (12)

1. A method of treating agitation associated with schizophrenia or bipolar I or II disorder in a human subject comprising:

administering a first dose of dexmedetomidine or a pharmaceutically acceptable salt thereof in an oromucosal formulation to the human subject;

optionally administering a second dose of dexmedetomidine or a pharmaceutically acceptable salt thereof in an oromucosal formulation that is administered to the human subject at least two hours after and within 24 hours of the first dose and wherein the second dose is 60 mcg of dexmedetomidine;

optionally administering a third dose of dexmedetomidine or a pharmaceutically acceptable salt thereof in an oromucosal formulation that is administered to the human subject at least two hours after the second dose and within 24 hours of the first dose and wherein the third dose is 60 mcg of dexmedetomidine;

wherein the human subject has a severe hepatic impairment and the agitation is mild or moderate; and

wherein the first dose is 60 mcg of dexmedetomidine or the equivalent amount of a pharmaceutically acceptable salt thereof;

wherein the maximum daily dose is 180 mcg.

2. The method of claim 1 , wherein the oromucosal formulation further comprises at least one water-soluble polymer.

3. The method of claim 2 , wherein the at least one water-soluble polymer is selected from the group consisting of hydroxypropyl cellulose, hydroxypropyl methylcellulose, hydroxyethyl cellulose, carboxy methylcellulose, methylcellulose, polyethylene oxide (PEO), and mixtures thereof.

4. The method of claim 3 , wherein the at least one water-soluble polymer is hydroxypropyl cellulose.

5. The method of claim 1 , wherein the second dose of dexmedetomidine or a pharmaceutically acceptable salt thereof is administered and is 60 mcg of dexmedetomidine or the equivalent amount of a pharmaceutically acceptable salt thereof.

6. The method of claim 5 , wherein the third dose of dexmedetomidine or a pharmaceutically acceptable salt thereof is administered and is 60 mcg of dexmedetomidine or the equivalent amount of a pharmaceutically acceptable salt thereof.

Assignments (3)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jun 29, 2026
From: E.Z. BIOXCEL SOLUTIONS PVT. LTD.
To: BIOXCEL THERAPEUTICS, INC.
Reel/Frame 075124/0786 →
SECURITY INTEREST Recorded Sep 11, 2024
From: BIOXCEL THERAPEUTICS, INC.
To: OAKTREE FUND ADMINISTRATION, LLC
Reel/Frame 068938/0906 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 12, 2024
From: KAKUMANU, VASUKUMAR; HANLEY, DAVID CHRISTIAN; YOCCA, FRANK; LATHIA, CHETAN DALPATBHAI; RAJACHANDRAN, LAVANYA; RISINGER, ROBERT
To: BIOXCEL THERAPEUTICS, INC.
Reel/Frame 067086/0078 →
Continuity (3)
Continuation 18189073 · Mar 23, 2023
Continuation 18153870 · Jan 12, 2023
Related Publication 20240252471A1 · Aug 1, 2024