India-based Hetero's Paxlovid generic gets WHO backing
Send a link to a friend
[December 28, 2022]
(Reuters) - India's Hetero said on Tuesday that its generic
version of Paxlovid, an antiviral treatment for COVID-19 developed by
Pfizer Inc, was added to the World Health Organization's
prequalification list, which serves as a benchmark for procurement of
medicines by developing countries.
Hetero said it had entered into a licensing agreement with the United
Nations-backed Medicines Patent Pool (MPP) to manufacture and sell the
generic version of the drug in low- and middle-income countries.
The treatment bundles two nirmatrelvir pills and one ritonavir pill and
will be manufactured at Hetero's plants in India, where the drug has
emergency use authorization from the country's drugs controller general.
[to top of second column]
|
The World Health Organization logo is
pictured at the entrance of the WHO building, in Geneva,
Switzerland, December 20, 2021. REUTERS/Denis Balibouse
The global health agency has
strongly recommended the use of Pfizer's Paxlovid for treating
high-risk patients with mild and moderate COVID, while expressing
concerns regarding its access in low- and middle-income countries.
(Reporting by Bhanvi Satija in Bengaluru; Editing by Shailesh Kuber
and Anil D'Silva)
[© 2022 Thomson Reuters. All rights
reserved.] This material may not be published,
broadcast, rewritten or redistributed.
Thompson Reuters is solely responsible for this content. |