New Delhi
Eli Lilly and Company India said on Tuesday it has received permission for restricted emergency use of its antibody drugs bamlanivimab 700 mg and etesevimab 1,400 mg in India for treatment of patients with mild to moderate Covid-19.
Both drugs together are indicated for restricted use in emergency situation, IV route for the treatment of mild to moderate Covid-19 for injection administration in hospital settings in adults and pediatric patients.
Lilly said it is engaging in active dialogue with the Indian government and regulatory authorities to donate bamlanivimab and etesevimab to speed up access and provide treatment options for patients with Covid-19.
The drugs together have been authorised under emergency use authorisation in the US and select European Union countries.
Antibody cocktail treatment begins at Delhi’s Ganga Ram
The Sir Ganga Ram Hospital on Tuesday started administering monoclonal antibody cocktail (MAC) to coronavirus patients, the medical facility said. It is administering a combination of casirivimab and imdevimab to consenting patients with mild and moderate Covid-19 symptoms at high risk of developing serious illness, it added. The MRP of one MAC dose for a patient is Rs59,750, the statement said.The Sir Ganga Ram Hospital on Tuesday started administering monoclonal antibody cocktail (MAC) to coronavirus patients, the medical facility said. It is administering a combination of casirivimab and imdevimab to consenting patients with mild and moderate Covid-19 symptoms at high risk of developing serious illness, it added. The MRP of one MAC dose for a patient is Rs59,750, the statement said.
Biological E ties up with Canada’s Providence to produce mRNA vaccine
Hyderabad: Biological E Limited has tied up with Canada’s Providence Therapeutics to locally manufacture its mRNA coronavirus vaccine, the Hyderabad-based firm said on Tuesday, adding it will run a pivotal trial in India, and seek emergency-use authorisation. As per Biological E, the term sheet sets forth the material terms for a definitive licensing and collaboration agreement and also outlines the terms for sale by Providence of up to 30 million doses of Providence’s proprietary messenger RNA vaccine, PTX-COVID19-B, to Biological E and other end-buyers.
Biological E Limited will run a pivotal trial in India and seek EUA, it added.