BRUSSELS: Nearly 30 generic drugmakers in Asia, Africa and the Middle East will make cheap versions of Merck & Co’s Covid-19 pill, under a landmark UN-backed deal to give poorer nations wider access to a drug seen as a weapon in fighting the pandemic.
Merck’s early greenlight to production of its anti-viral pill molnupiravir by other companies during the pandemic is a rare example in the pharmaceutical sector, which usually protects its patented treatments for longer periods.
However, there are questions about molnupiravir which has shown low efficacy in trials and has raised concerns for side-effects, and lengthy procedures for appovals may delay supplies in many poorer nations for months.
Under the deal, negotiated by the UN-backed Medicines Patent Pool (MPP) with Merck, the US company will not receive royalties for the sale of the low-cost version of the pill while the pandemic continues.
The MPP said the deal stipulated the pill would be distributed to 105 less-developed nations.
A molnupiravir course of 40 pills for five days is expected to cost about $20 in poorer nations, an MPP official involved in the talks with drugmakers told Reuters, citing initial estimates from drugmakers, which are subject to change.
That is far below the $700 per course the United States agreed to pay for an initial delivery of 1.7 million courses, but twice as high as first estimated by the World Health Organization (WHO)-backed programme to procure Covid-19 drugs and vaccines for the world.
The new agreement allows 27 generic drugmakers from India, China and other countries in Africa, Asia and the Middle East to produce ingredients and the finished drug. An MPP spokesperson said deliveries from some firms covered by the deal could start as early as February. However, that will be subject to regulatory approval.
While molnupiravir is in use in the United States after approval in December, some other Western countries have cancelled or are reconsidering orders after the drug showed low efficacy in trials.
Molnupiravir has also not been approved by the World Health Organization, which makes its sale at the moment not possible in most developing countries with limited regulatory resources for national authorisations.
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