IP Library Granted Patent US 12,133,912
Granted Patent B2
US 12,133,912 · App. 18/528,684 · Granted Nov 5, 2024

Stable pharmaceutical compositions of succinylcholine chloride

Inventors: Ashish Anilrao Dubewar (Hyderabad, IN); Amit Anil Charkha (Wardha, IN); Sumitra Ashokkumar Pillai (Hyderabad, IN); Pradeep Kumar Kare (Hyderabad, IN); Kumar Swamy Ummiti (Hyderabad, IN); Shanker Mamidi (Nalgonda, IN); Mayur Anshiram Adhav (Hyderabad, IN)
Assignee: Slayback Pharma LLC.
A61K9/0019A61K31/221A61K31/225A61K47/10A61K47/12A61K47/183
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Quick Facts
Patent No.
US 12,133,912
App. No.
18/528,684
Granted
Nov 5, 2024
Kind
B2
Abstract

The present invention relates to injectable pharmaceutical compositions comprising therapeutically effective amount of succinylcholine chloride, one or more pharmaceutically acceptable aqueous solvents, and one or more stabilizing agents selected from aliphatic polyols; lower alkyl alcohols; amino acids having at least one additional amino, carboxyl or hydroxyl group; amino alcohols; and aliphatic dicarboxylic acids having at least one hydroxyl or amino group, or α-β unsaturation. The compositions are stable at room temperature for at least 30 days. Methods of manufacturing the injectable pharmaceutical compositions are also provided. The composition may be provided in a sealed container, e.g., an ampoule, vial and pre-filled syringe, and are suitable for subcutaneous, intravenous or intramuscular administration as an adjunct to general anesthesia, to facilitate tracheal intubation, and/or to provide skeletal muscle relaxation during surgery or mechanical ventilation.

Claims (8)

1. A pharmaceutical composition consisting of:

(i) therapeutically effective amount of succinylcholine chloride at a concentration of from about 5 mg/mL to 60 mg/mL;

(ii) propylene glycol as a stabilizing agent at a concentration of from about 20 mg/mL to about 300 mg/mL;

(iii) water as a solvent,

(iv) optionally one or more pH adjusting agents; and

(v) optionally sodium chloride as a tonicity contributing agent at a concentration of from about 1 mg/mL to about 50 mg/mL,

wherein the composition is in the form of a ready to use aqueous solution suitable for parenteral administration, and

wherein the aqueous solution is stable at room temperature for at least 30 days.

Assignments (3)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 18, 2025
From: SLAYBACK PHARMA LIMITED LIABILITY COMPANY
To: AZURITY PHARMACEUTICALS, INC.
Reel/Frame 070877/0696 →
CONFIRMATORY GRANT OF SECURITY INTEREST IN UNITED STATES PATENTS Recorded Mar 17, 2025
From: ARBOR PHARMACEUTICALS, LLC; AZURITY PHARMACEUTICALS, INC.; AZURITY PHARMACEUTICALS IRELAND LIMITED; SILVERGATE PHARMACEUTICALS, INC.
To: HPS INVESTMENT PARTNERS, LLC, AS ADMINISTRATIVE AGENT
Reel/Frame 070531/0487 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 19, 2024
From: CHARKHA, AMIT ANIL; PILLAI, SUMITRA ASHOKKUMAR; KARE, PRADEEP KUMAR; UMMITI, KUMAR SWAMY; MAMIDI, SHANKER; ADHAV, MAYUR ANSHIRAM; DUBEWAR, ASHISH ANILRAO
To: SLAYBACK PHARMA LLC
Reel/Frame 066180/0632 →