This site is intended for Healthcare Professionals only.

Glenmark launches tablet to control type 2 diabetes in India which costs just £0.16

Date:

Share post:

Glenmark Pharmaceuticals has launched a fixed-dose combination drug for the management of type 2 diabetes patients in India which costs just £0.16 per tablet.

According to a statement issued by Glenmark Pharmaceuticals Limited, the company has launched a fixed-dose combination (FDC) of its novel, patent-protected, globally-researched Sodium-Glucose Co-Transporter Inhibitor (SGLT2i) – Remogliflozin Etabonate and another widely used DPP4 inhibitor (Dipeptidyl Peptidase 4 inhibitor) – Vildagliptin, with Metformin (first-line medication for the treatment of type 2 diabetes).

“The combination contains Remogliflozin (100 mg) + Vildagliptin (50 mg) + Metformin (500/1000 mg) in a fixed-dose and must be taken twice daily to improve glycemic control in patients. Glenmark has launched the same under two brand names Remo MV and Remozen MV,” said the statement.

With the launch of Remogliflozin-Vildagliptin-Metformin fixed-dose combination (FDC), Glenmark has become the first country in the world to do so and India becomes the first country to gain access to this FDC drug.

“Glenmark received approval from the DCGI (the drug approval authority in India) for manufacturing and marketing this fixed-dose combination in late September 2021,” said the statement.

Globally preferred treatment option

Glenmark, in its release, said that SGLT2 inhibitors and DPP4 inhibitors are emerging as the preferred treatment option for the management of type 2 diabetes globally.

Glenmark’s FDC of Remogliflozin-Vildagliptin-Metformin tackles most of the pathophysiology in type 2 diabetes that makes it an appealing fixed-dose combination in managing uncontrolled type 2 diabetes.

“Mono components of the FDC are recommended by AACE guidelines for early use in the hierarchy of Antidiabetic medications for the management of type 2 diabetes. Further, FDC of SGLT2i + DPP4i + Metformin is currently first and only triple-drug FDC considered rationale for approval by US FDA,” said the statement.

The statement further said: “This combination has been approved by the DCGI, the drug regulator in India, for adults aged 18 years and older with type 2 diabetes to improve glycemic control when metformin and one of the mono-components of fixed-dose combination do not provide adequate glycemic control, or when already being treated with separate doses of Remogliflozin, Vildagliptin and Metformin.

“We are proud to introduce this innovative fixed-dose combination, which is cutting-edge, extensively researched, at an affordable cost and will significantly improve patient compliance and provide glycemic and extra glycemic benefits to patients with uncontrolled type 2 diabetes, in India,” said the group vice president and business head, India Formulations, Alok Malik.

LEAVE A REPLY

Please enter your comment!
Please enter your name here

Current Issue March 2024

Related articles

Boots supports community pharmacists become Mental Health First Aiders

PDA encourages representatives at Boots to undertake Mental Health First Aid (MHFA) training Pharmacists, who are working on the...

Surge in stroke cases could cost UK £75bn by 2035, charity warns

By 2035, there will be 151,000 hospital admissions due to stroke every year, averaging 414 admissions per day...

NHS and i.AI forge historic collaboration to boost healthcare

AI assisting NHS to half treatment times for stroke patients and overall patient care experience The Department of Health...

NHS to cut the red tape to support 50K NHS postgraduate doctors

New measures are part of NHS' broader efforts to retain its skilled workforce and ensure high-quality patient care  In...