Hindustan Times ST (Jaipur)

Roche, Cipla launch antibody drug in India, to cost ₹59k per dose

- Press Trust of India

THE ANTIBODY COCKTAIL IS TO BE ADMINISTER­ED FOR TREATING MILD TO MODERATE COVID-19 CASES

NEW DELHI: Drug majors Roche India and Cipla on Monday announced launch of Roche’s Antibody Cocktail in India priced at ₹59,750 per dose for the treatment of mild to moderate COVID-19 in patients who are at high risk.

“The first batch of the Antibody Cocktail (Casirivima­b and Imdevimab) is now available in India while a second batch will be made available by mid-june. In total they can potentiall­y benefit 2,00,000 patients as each of the 1,00,000 packs that will be available in India offers treatment for two patients,” Cipla and Roche said in a joint statement. Cipla will distribute the product by leveraging its strong distributi­on strengths across the country, it added.

The price for each patient dose [a combined dose of 1,200 mg (600 mg of Casirivima­b and 600 mg of Imdevimab)] will be ₹59,750 inclusive of all taxes. The maximum retail price for the multi dose pack (each pack can treat two patients) is ₹1,19,500 inclusive of all taxes As per the statement, the drug will be available through leading hospitals and COVID treatment centers. The Central Drugs Standards Control Organisati­on (CDSCO) had recently provided an emergency use authorisat­ion (EUA) for the Antibody Cocktail (Casirivima­b and Imdevimab) in India. It has also received a EUA in the US and several EU countries. “We are optimistic that the availabili­ty of Antibody Cocktail (Casirivima­b and Imdevimab) in India can help in minimising hospitalis­ation, ease the burden on healthcare systems and play a key role in treatment of high risk patients before their condition worsens,” said V Simpson Emmanuel, Managing Director and CEO, Roche Pharma India. ‘’ Umang Vohra, MD and Global CEO Cipla said we look forward to leveraging our solid marketing and distributi­on strengths in India to provide broader, equitable access to this innovative treatment option in the country. The drug is to be administer­ed for the treatment of mild to moderate COVID-19 in adults who are confirmed to be infected and who are at high risk of developing severe disease and do not require oxygen.

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