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Indian firm launches Merck’s Covid pill under brand name ‘molulife’

Over a dozen Indian companies have publicly stated they will produce the pill, the patent for which was freed for low- and middle-income countries by the American pharma firm under the United Nations Medicines Patent Pool.

Updated on: Dec 30, 2021, 04:31:51 IST
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Drug major Mankind Pharma and generics maker BDR pharmaceuticals on Wednesday announced launch of Merck’s oral Covid-19 anti-viral pill Molnupiravir under the brand name Molulife.

A health worker administers Covid-19 vaccine to a beneficiary at Chembur Vaccination center in Mumbai on Wednesday. (Satish Bate/HT Photo)
A health worker administers Covid-19 vaccine to a beneficiary at Chembur Vaccination center in Mumbai on Wednesday. (Satish Bate/HT Photo)

Over a dozen Indian companies have publicly stated they will produce the pill, the patent for which was freed for low- and middle-income countries by the American pharma firm under the United Nations Medicines Patent Pool.

India’s drugs controller general of India, VG Somani, approved Molnupiravir on Tuesday for restricted emergency use in the country to treat mild to moderate Covid-19 patients.

The drug inhibits the replication of the Covid-19 causing Sars-CoV-2 virus by introducing errors in its genetic code. It needs to be given early in the infection cycle.

“This launch further enhances the Covid-19 treatment portfolio in BDR’s product basket with the addition of generic Molnupiravir. We are pleased to collaborate with Mankind Pharma to take one step forward in fighting the virus. At this point of time, the nation needs such drugs that can effectively help in fighting the cases,” said Raheel Shah, director, business development, BDR Pharma.

The tie-up between Mankind and BDR is a licensing arrangement where production is by BDR Pharma and marketing, selling, promotion, distribution will be done by Mankind.

According to a company statement, Mankind, in partnership with BDR, plans to make Molulife available at mass scale. “A pill for Covid-19 is bound to go miles in strengthening defenses against Covid-19 battle… will make Molulife available in every nook and corner of the country. The company (is) focusing on providing a range of medicines for the management and treatment of Covid-19 in India,” said Sanjay Koul, senior president, sales and marketing, Mankind Pharma.

Earlier this month, the drug, developed by Merck in collaboration with Ridgeback Biotherapeutics, was approved by the the UK Medicines and Healthcare Products Regulatory Agency (MHRA) and the US Food and Drug Administration (USFDA).

The other Covid-19 pill approved by these countries is Pfizer’s Paxlovid.

According to Union health ministry, Central Drugs Standard Control Organisation received 22 applications for manufacture and market of the drug in the country, of which eight including five applicants of a consortium (total 13) submitted their interim or complete clinical trial report. Considering the emergency and unmet medical need in Covid-19, the Subject Expert Committee recommended permission to manufacture and market be granted, the government said.

“Only when the data seemed satisfactory and all conditions were met that the approval was granted. The regulator wanted to be sure that they were not over-estimating the drug’s efficacy that could have led to rise in false expectations,” said a senior government official aware of the matter, on condition of anonymity.

Other Indian companies that received the approval too are readying for a launch of their own versions of the drug, with most likely to go to market in January, 2022. “…Marketed under the brand name Molunamax, it will soon be available all across the country in the next month for the treatment of mild Covid-19..,” said JB Chemicals and Pharmaceuticals in a statement.

  • Rhythma Kaul
    ABOUT THE AUTHOR
    Rhythma Kaul

    Rhythma Kaul is the national health editor of the Hindustan Times. She has been reporting on public health, medicine, and medical research, with a particular focus on how government decisions and health system reforms shape people’s lives. Rhythma has over 25 years of journalistic experience. She joined Hindustan Times in 2008, and has since covered everything from pandemics and infectious diseases to cutting‑edge medical research and climate‑related health challenges. Her stories routinely track the work of the Ministry of Health and Family Welfare, department of pharmaceuticals, and key national health programmes, making complex medical science and policy accessible to a wide audience. One of her prominent news breaks has been the 2012 Baby Falak case: A two-year-old brutally battered baby girl was admitted to AIIMS-Delhi with severe head injuries, multiple fractures, human bite marks, and burns. The police investigation revealed this to be a case of multi-state human-trafficking racket. She was profiled by The Wall Street Journal for breaking this story. Rhythma holds a Master’s degree from Jawaharlal Nehru University, Delhi. Prior to Hindustan Times, she worked with the India Today Group. Rhythma can be contacted at rhythma.kaul@hindustantimes.com. Her X handle is @RamblingBrook.Read More