Baricitinib: BDR Pharma signs licensing agreement with Lilly

Lilly received permission for restricted emergency use from the Central Drugs Standard Control Organization, a division of the Ministry of Health.

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Deal
Picture: Pixabay

BDR Pharma has entered into a royalty-free, limited and non-exclusive voluntary licensing agreement with Eli Lilly and Company, for the manufacturing and distribution of baricitinib for the treatment of C-19 in India.

Baricitinib received restricted emergency use approval, for use in combination with remdesivir, for treatment of suspected or laboratory-confirmed coronavirus disease 2019 (C-19) in hospitalized adults and pediatric patients two years of age or older, requiring supplemental oxygen, invasive mechanical ventilation, or extracorporeal membrane oxygenation (ECMO).

Medicine Tablet
Picture: Pixabay

Lilly received permission for restricted emergency use from the Central Drugs Standard Control Organization (CDSCO), a division of the Ministry of Health.

“We are swiftly working to ensure high-quality manufacturing and equitable access of Baricitinib for C-19 in India. We will continue to explore other possible initiatives to support patients and the healthcare system in India.” – Luca Visini, MD, India Subcontinent, Lilly India

Commenting on the development and the royalty-free non-exclusive voluntary license with Lilly, Dharmesh Shah, Chairman, BDR Pharmaceuticals, said, “We hope this collaboration will address more unmet medical needs by broadening and deepening the discovery and development of C-19 treatments options.”

BDR has applied for restricted emergency use approval with the Drug Controller General of India (DCGI) for baricitinib for C-19 in India. Lilly had recently announced seven voluntary license agreements with major local generic drug manufacturers in India for the production of the same.


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