IP Library › Granted Patent US 12,734,188
Granted Patent B2
US 12,734,188 · App. 18/580,779 · Granted Sep 15, 2026

Pharmaceutical composition comprising combination of sitagliptin and empagliflozin

Inventors: Balvir Singh (Ahmedabad, IN); Ramesh Shingala (Ahmedabad, IN); Milap Patel (Gandhinagar, IN); Ritesh Patel (Ahmedabad, IN)
Assignee: UNISON PHARMACEUTICALS PVT. LTD.
A61K31/7048A61K9/2009A61K9/2018A61K9/2054A61K9/209A61K31/4985A61K47/183
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Quick Facts
Patent No.
US 12,734,188
App. No.
18/580,779
Granted
Sep 15, 2026
Kind
B2
Abstract

The present invention relates to a stable pharmaceutical composition comprising a fixed dose combination of a therapeutically effective amount of DPP-IV inhibitor and a therapeutically effective amount of SGLT2 inhibitor for reducing blood glucose level in patients with diabetes. The present invention specifically relates to a stable pharmaceutical composition comprising Sitagliptin or a pharmaceutically acceptable salts or solvate or hydrate or premix thereof and Empagliflozin or a pharmaceutically acceptable salt or solvate or hydrate or premix thereof in the presence of one or more pharmaceutically acceptable excipients. Moreover, the present invention relates to a stable pharmaceutical composition comprising Sitagliptin Phosphate Monohydrate, Empagliflozin and one or more pharmaceutically acceptable excipients with high content uniformity, reduced degradation impurities and optimum dissolution.

Claims (8)

1 . A stable pharmaceutical composition comprising a combination of Sitagliptin or pharmaceutically acceptable salt or solvate thereof with Empagliflozin or pharmaceutically acceptable salt or solvate thereof and at least one or more pharmaceutically acceptable excipients, wherein the pharmaceutical composition comprises a first portion and a second portion, wherein the first portion comprises Sitagliptin or pharmaceutically acceptable salt or solvate thereof in the form of powder or granules along with one or more pharmaceutically acceptable excipients, and the second portion comprises Empagliflozin or pharmaceutically acceptable salt or solvate thereof in the form of powder or granules along with one or more pharmaceutically acceptable excipients.

2 . The stable pharmaceutical composition as claimed in claim 1 , wherein the composition is in the form of single layer or bilayer tablet.

3 . The stable pharmaceutical composition as claimed in claim 2 , wherein the pharmaceutically acceptable excipient is selected from the group consisting of diluent, binder, disintegrant, stabilizer, lubricant, glidant, colouring agent, film coating agent and a combination thereof.

4 . The stable pharmaceutical composition as claimed in claim 3 , wherein the composition, when stored at 40° C. and 75% relative humidity, contains not more than 0.2% of any known or unknown impurity and not more than 2% of the total impurity for Sitagliptin; and contains not more than 0.5% of any known impurity, not more than 0.2% of any unknown impurity and not more than 2% of total impurity for Empagliflozin.

5 . The stable pharmaceutical composition as claimed in claim 1 , wherein at least 75% of Sitagliptin and Empagliflozin are released within 30 minutes.

6 . The stable pharmaceutical composition as claimed in claim 1 , wherein the composition comprises 10-40% w/w Sitagliptin, 1-10% w/w Empagliflozin, 5-80% w/w of diluent, 1-10% w/w of disintegrant, 1-10% w/w binder, 0-10% w/w stabilizer, 0.1-5% lubricant, 0.1-5% w/w glidant and 1-10% w/w of film former of the total weight of the composition.

7 . The stable pharmaceutical composition as claimed in claim 6 , wherein the stabilizer is selected from the group consisting of acidic agent, alkalizing agent, buffering agent, amino acid, anti-oxidant, and a combination thereof.

8 . The stable pharmaceutical composition as claimed in claim 7 , wherein the stabilizer is L-Arginine.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 21, 2024
From: SINGH, BALVIR; SHINGALA, RAMESH; PATEL, MILAP; PATEL, RITESH
To: UNISON PHARMACEUTICALS PVT. LTD.
Reel/Frame 066190/0648 →
Priority Claims (1)
IN 202121046486 · Oct 12, 2021 · national
Continuity (1)
Related Publication 20240374627A1 · Nov 14, 2024
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