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India Gives Emergency Approval to Eli Lilly’s Drugs To Treat COVID

Bamlanivimab and etesevimab together can be administered via injection in a restricted manner.

Published
COVID-19
2 min read
Eli Lilly receives emergency-use approval for antibody drugs to treat COVID-19 in India.
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American pharmaceutical company Eli Lilly has announced that it has received permission for restricted emergency use of its antibody drugs, bamlanivimab 700mg and etesevimab 1400mg, in India for the treatment of patients with mild to moderate coronavirus.

Bamlanivimab and etesevimab together are indicated for restricted use in emergency situation, IV route for the treatment of mild to moderate coronavirus disease for injection administration in hospital setting.

The injection can be administered in adults and pediatric patients (12-year-olds and those weighing at least 40 kg) with RT-PCR positive results of direct SARS-CoV-2 viral testing and who are at high risk for progressing to severe COVID-19 and/or hospitalisation and do not require oxygen.

Lilly is engaging in active dialogue with the Indian government and regulatory authorities to donate bamlanivimab and etesevimab, in order to speed up access and provide treatment options for patients with COVID-19, the company said in a statement.

Bamlanivimab and etesevimab together have been authorised under Emergency Use Authorisation in the US and select EU countries, for the treatment of mild to moderate COVID-19.

Speaking about its benefits for patients with COVID-19, Luca Visini, Managing Director, India Subcontinent, Lilly India, said, “We are pleased that we have another innovative treatment option to offer India's healthcare providers who continue to be at the forefront of the battle against COVID-19. Lilly is committed to contributing to the alleviation of the COVID-19 pandemic in India and around the world. We will continue to assess and evaluate how our existing portfolio and ongoing research can benefit patients with COVID-19.”

Earlier in May, Lilly had also received permission for the emergency use of baricitinib in combination with Remdesivir, for the treatment of suspected or laboratory confirmed coronavirus 2019 (COVID-19 in hospitalised adults requiring supplemental oxygen, invasive mechanical ventilation, or extracorporeal membrane oxygenation, ECMO).

Since then, Lilly has already made available a donation of more than 6,50,000 tablets of Baricitinib to the Indian government and issued eight voluntary licenses to Indian pharmaceutical manufacturers of generic medicines to accelerate and expand the availability of baricitinib to patients in India.

(At The Quint, we are answerable only to our audience. Play an active role in shaping our journalism by becoming a member. Because the truth is worth it.)

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