Bajaj Healthcare Limited has secured CDSCO approval on December 31, 2025, to launch Phase III clinical trials and bioequivalence studies for Suvorexant Tablets, building on prior SEC recommendation. This insomnia treatment innovation positions the firm as India's pioneer in this therapy, paving the way for market entry after proving efficacy and safety.
Bajaj Healthcare Limited announced a pivotal regulatory milestone today, receiving formal approval from the Central Drugs Standard Control Organisation (CDSCO) to proceed with Clinical Trial and Bioequivalence Study for Suvorexant Tablets. This follows the Subject Expert Committee (SEC) on Neurology & Psychiatry's positive recommendation, confirming the company's readiness for advanced testing of the insomnia drug in strengths like 5mg, 10mg, 15mg, and 20mg. Suvorexant targets sleep-wake cycle modulation via the central nervous system, addressing a key need in adult insomnia management.
Key Developments
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Received CDSCO nod to conduct Phase III trials and BE study on December 31, 2025
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First Indian firm pioneering Suvorexant development per SEC clearance
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Trials to assess efficacy, safety, tolerability in diverse patients before market approval
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Enables robust R&D push in CNS disorders with GMP facilities
Sources: Marketscreener.com, Bajajhealth.com (official filings),
Stockinsights.ai