IP Library › Granted Patent US 12,685,728
Granted Patent B2
US 12,685,728 · App. 18/033,993 · Granted Jul 21, 2026

Anti-vertigo compound and pharmaceutical compositions thereof

Inventor: Nirav Vyas (Ahmedabad, IN)
Assignee: AMNEAL PHARMACEUTICALS LLC
A61K31/4453A61K9/0053A61P1/08
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Quick Facts
Patent No.
US 12,685,728
App. No.
18/033,993
Filed
Apr 26, 2023
Granted
Jul 21, 2026
Kind
B2
Art Unit
1691
USPC
514/317
Abstract

The present invention relates to uses of Levocloperastine for the treatment or prevention of vertigo, disease associated with vertigo or symptoms associated therewith. Further, the invention also relates to oral pharmaceutical composition comprising Levocloperastine and one or more pharmaceutical excipients and its preparation process.

Claims (15)

1 . A method of treatment of vertigo, one or more symptoms of vertigo, or a disease associated with vertigo in a human subject, wherein the method comprises administering to the subject a therapeutically effective amount of levocloperastine or a pharmaceutically acceptable salt thereof.

2 . The method according to claim 1 , wherein the one or more symptoms of vertigo or the disease associated with vertigo are selected from the group consisting of Peripheral Vertigo, Meniere's disease, Tinnitus, Hearing loss, Giddiness, Dysesthesia of motion and position, Nystagmus, Dysequilibrium, Dizziness, Head deviation, Nausea, Vomiting, Sweating, Salivation and Tachycardia, Dysstasia and Walking unsteadiness, Staggering, Rotary sensation, Tendency to fall, Lift sensation, Blackout, Change of position (lying), Bowing, Getting up, driving, Head movements (inclination, twist), and eye movement.

3 . The method according to claim 1 , wherein levocloperastine or a pharmaceutically acceptable salt thereof is administered at a daily dose of about 10-1000 mg.

4 . The method according to claim 3 , wherein levocloperastine or a pharmaceutically acceptable salt thereof is administered at a daily dose of about 10-100 mg.

5 . The method according to claim 4 , wherein levocloperastine or a pharmaceutically acceptable salt thereof is administered at a daily dose of about 10-80 mg.

6 . The method according to claim 1 , wherein levocloperastine or a pharmaceutically acceptable salt thereof is administered in an amount from about 60-90 mg once daily, or about 30-45 mg twice a day, or about 20-30 mg thrice a day.

7 . The method according to claim 1 , wherein levocloperastine or a pharmaceutically acceptable salt thereof is administered in an amount of from about 70-120 mg once daily, or about 35-60 mg twice a day, or about 25-40 mg thrice a day.

8 . The method according to claim 1 , wherein levocloperastine or a pharmaceutically acceptable salt thereof is administered in an amount from about 90-160 mg once daily, or about 45-80 mg twice a day, or about 30-55 mg thrice a day.

9 . The method according to claim 1 , wherein levocloperastine or a pharmaceutically acceptable salt thereof is administered in an amount of from about 20-30 mg three times a day.

10 . The method according to claim 1 , wherein levocloperastine or a pharmaceutically acceptable salt thereof is administered in an amount of from about 30-55 mg three times a day.

11 . The method according to claim 1 , wherein levocloperastine is administered for a duration of the treatment that is shorter as compared to the standard of care therapy.

12 . The method according to claim 11 , wherein the standard of care therapy is selected from one or more of betahistine 16 mg tablets three times daily or betahistine 16 mg tablets three times daily plus acetazolamide 125 mg tablets two time daily or cinnarizine 25 mg tablets three times daily.

13 . The method according to claim 1 , wherein levocloperastine or a pharmaceutically acceptable salt is administered in a pharmaceutical composition.

14 . The method according to claim 13 , wherein the pharmaceutical composition is an oral composition.

15 . The method according to claim 14 , wherein the oral composition a tablet, capsule, granules, powder, solution, syrup, emulsion or suspension composition.

Assignments (3)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 14, 2025
From: KASHIV BIOSCIENCES, LLC
To: SHIVANKA RESEARCH, LLC
Reel/Frame 071115/0589 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 14, 2025
From: SHIVANKA RESEARCH, LLC
To: AMNEAL PHARMACEUTICALS LLC
Reel/Frame 071115/0600 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Aug 14, 2023
From: VYAS, NIRAV
To: KASHIV BIOSCIENCES, LLC
Reel/Frame 064578/0663 →
Priority Claims (1)
IN 202021047025 · Oct 28, 2020 · national
Continuity (1)
Related Publication 20230390271A1 · Dec 7, 2023
References Cited (10)
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Zoic's ASTARIL-LR. [cited by examiner]
International Search Report dated Dec. 29, 2021, for corresponding International Patent Application No. PCT/IN2021/050886. [cited by applicant]
Written Opinion dated Dec. 29, 2021, for corresponding International Patent Application No. PCT/IN2021/050886. [cited by applicant]
Aliprandi et al., (2002). “Therapeutic Use of Levocloperastine as an Antitussive Agent: An Overview of Preclinical Data and Clinical Trials in Adults and Children.” Clinical Drug Investigation. 22. 209-220. [cited by applicant]
Dyhrfjeld-Johnsen et al., (2019) “Management of peripheral vertigo with antihistamines: New options on the horizon.” Br J Clin Pharmacol. 85. 2255-2263. [cited by applicant]