Business Standard

India closer to getting Merck’s new Covid drug molnupirav­ir

- SOHINI DAS Mumbai, 2 December

With the expert group having advised the US regulator to recommend the use of Merck’s antiviral drug molnupirav­ir for Covid, drug makers here are awaiting a final decision from the Indian regulator.

Molnupirav­ir approval assumes significan­ce. It could offer an affordable oral drug to treat Covid. The drug developed by Merck with Ridgeback Biotherape­utics targets part of the virus called the ribonuclei­c acid polymerase. This part of the virus has not changed much after mutations in the Omicron variant.

However, according to the recent data published by Merck, the drug was found to be significan­tly less effective than previously thought. It reduced hospitalis­ations and deaths in its clinical trial of highrisk individual­s by around 30 per cent.

The subject expert committee (SEC) that is advising the Drugs Controller General of India (DCGI) had sought more data from a consortium of drugmakers — Dr Reddy’s Laboratori­es (DRL), Torrent

Pharmaceut­icals, Emcure Pharmaceut­icals, Sun Pharmaceut­ical Industries (Sun Pharma), and Cipla — in its last meeting.

“In its last meeting, the SEC had requested more data from all companies. On behalf of the consortium, we have submitted the data. We now await the next SEC meeting,” said a spokespers­on for DRL.

These five drugmakers had come together in June to jointly sponsor, supervise, and monitor the clinical trial in India. Between March and April this year, these five pharmaceut­ical companies had individual­ly entered into a non-exclusive voluntary licensing agreement with Merck Sharp Dohme (MSD) to manufactur­e and supply molnupirav­ir to India and over 100 low- and middle-income countries. This apart, drugmakers like Hetero Labs have also done trials independen­tly on molnupirav­ir here.

An expert panel of advisors to the US Food and Drug Administra­tion (USFDA) on Tuesday voted to recommend the authorisat­ion of Merck's antiviral pill for treatment of Covid. Last year, the USFDA had authorised the use of Gilead Sciences, Inc.’s injectable antiviral remdesivir to treat Covid. In November, Sun Pharma had said that it was gearing up to launch molnupirav­ir under the brand name Molxvir in India. Molnupirav­ir is the first oral antiviral approved by the UK’S Medicines and Healthcare products Regulatory Agency for the treatment of mild-tomoderate Covid in adults. Kirti Ganorkar, chief executive officer of India business, Sun Pharma, had said, “The recent authorisat­ion of molnupirav­ir, licensed from MSD and Ridgeback by the UK regulator, is a positive step. In line with our consistent efforts to accelerate access to new drugs for Covid treatment, we are gearing up to make Molxvir available to patients and health care providers across India at an economical price after approval by the DCGI.

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