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Eli Lilly to transfer rights of two diabetes products to Cipla

NEW DELHI, Oct 4: Drug firm Eli Lilly and Company (India) on Monday said it has inked a pact with Cipla to enhance the reach of its two diabetes products ....

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Eli Lilly India gets nod for emergency use of antibody drugs combination for COVID-19

Bamlanivimab and etesevimab combination has been authorised under Emergency Use Authorisation in the US and select EU countries for the treatment of the disease. ....

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Eli Lilly India Receives Emergency Use Approval For Its Drug Combination Used To Treat Mild Covid Cases

The combination comprises two drugs bamlanivimab 700 mg and etesevimab 1400 mg, Eli Lilly India said

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Eli Lilly's antibody cocktail gets DCGI nod to treat moderate Covid

Eli Lilly and Company India on Tuesday said it has received permission for emergency use of its antibody drugs combination used for treatment of mild to moderate Covid-19, in the country.
The company has received permission for restricted emergency use of its monoclonal antibody drugs, bamlanivimab 700 mg and etesevimab 1400 mg, used together for the treatment of patients with mild to moderate Covid-19, Eli Lilly said in a statement.
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, it added. ....

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Eli Lilly's antibody cocktail drug gets emergency use nod in India

Eli Lilly s antibody cocktail drug gets emergency use nod in India
ANI |
Updated: Jun 01, 2021 17:59 IST
By Shalini Bhardwaj
New Delhi [India], June 1 (ANI): Eli Lilly and Company India on Tuesday announced that it has received emergency use approval in the country for its monoclonal antibody drug combination used for treating Covid-19 patients with mild to moderate symptoms.
The drug, a combination of Bamlanivimab 700 mg and Etesevimab 1400 mg has been approved for use in the country by the Drugs Controller General of India (DCGI).
This will be the second cocktail drug approved by DCGI for emergency use, after the drug regulator gave its nod to the antibody cocktail Casirivimab and Imdevimab developed by Roche. ....

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