India allows emergency use of Merck’s COVID-19 pill
Molnupiravir will be manufactured in India by 13 companies for restricted use under emergency situation for treatment of adult patients with COVID-19, Health Minister Mansukh Mandaviya said, reports Reuters.
Earlier this year, drugmakers Aurobindo Pharma, Cipla, Sun Pharmaceuticals and some others signed non-exclusive voluntary licensing agreements with Merck to manufacture and supply molnupiravir in India.
Last week, the US FDA issued a EUA to molnupiravir for the treatment of mild-to-moderate coronavirus disease in adults.
Media reports earlier in the day said the subject expert committee under the Central Drugs Standard Control Organisation recommended allowing EUA for molnupiravir, Covovax and Corbevax.
India is working on ramping up oxygen supplies and strengthening health infrastructure to contain a possible surge of COVID-19 cases due to the Omicron variant.
The country has administered 1.43 billion COVID-19 vaccine doses so far, with more than 839 million of all adults having received at least one dose.
India plans to start administering COVID-19 booster shots as a precautionary measure to healthcare and frontline workers from Jan. 10 and will begin vaccinating those aged 15-18 from Jan. 3.