Lupin to Conduct BE Study for Synthetic Semaglutide Tablets in 3 Strengths
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New Delhi: Lupin Limited has received the green light from the Subject Expert Committee (SEC) under the Endocrinology & Metabolism division of the Central Drugs Standard Control Organisation (CDSCO) to conduct a bioequivalence (BE) study for its synthetic Semaglutide Tablets in three dosage strengths - 3 mg, 7 mg, and 14 mg.
The proposal was reviewed at the SEC meeting following the company’s submission seeking permission to manufacture and market Semaglutide Tablets for the proposed indication. Lupin also presented the BE study protocol (Protocol No. 25-VIN-0292, Version 01, dated 16 May 2025) before the expert panel.
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