MSN Laboratories Launches ‘SEMABEST, the First Integrated Made-in-India Semaglutide

IMT News Desk
IMT News Desk
· 2 min read
MSN Laboratories launches SEMABEST: Dr. MSN Reddy, Bharat Reddy & Dr. Kamini Desai share views on the launch and on affordable diabetes care.

MSN Laboratories has launched SEMABEST, its semaglutide brand, in the Indian market following approval from the Central Drugs Standard Control Organisation (CDSCO).

SEMABEST is priced at nearly 50% lower than the innovator drug, significantly improving affordability and patient access. The therapy is available as a pre-filled pen for subcutaneous administration.

In this evolving landscape, SEMABEST stands apart with its strong backward integration across in-house USDMF-grade API and formulation. The Pen device is also manufactured in India and complies with global regulatory standards. SEMABEST represents a significant step forward in making complex peptide therapies more accessible, affordable, and scalable for Indian patients.

“The launch of SEMABEST marks a defining step in our journey to make next-generation metabolic therapies more accessible and affordable. As the burden of diabetes continues to rise, we remain focused on delivering high-quality, innovative solutions that can make a meaningful difference in patients’ lives,” said Dr. MSN Reddy, Founder & CMD, MSN Laboratories.

“MSN brings over a decade of expertise in complex peptide development, with its journey in this domain dating back to 2016 with the filing of its first USDMF for icatibant. Since then, the company has established a strong regulatory and scientific foundation, with 12 USDMFs for peptides and 6 US ANDAs for peptide formulations, supported by a broader portfolio of 560+ USDMFs and 400+ bioequivalent formulations globally. Leveraging its integrated R&D infrastructure and large-scale manufacturing capabilities, MSN is well positioned to ensure consistent supply, quality, and accessibility of SEMABEST across India,” said Bharat Reddy, Executive Director, MSN Laboratories.

“The product has demonstrated bioequivalence to the reference (innovator) drug, with its performance further validated through Phase III clinical studies conducted in direct comparison. The results showed comparable reduction in HbA1c levels, along with similar outcomes across key parameters including fasting plasma glucose (FPG), postprandial glucose (PPG) & weight loss. SEMABEST also exhibited a comparable safety profile, reinforcing its reliability as an effective therapeutic option,” said Dr Kamini Desai, Head- Medical Affairs, MSN Laboratories.

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