Merck seeks EU regulator nod for its Covid-19 pill

PTI Amsterdam | Updated on November 24, 2021

A decision could be made within weeks on whether it might be cleared, says EMA

The European Medicines Agency (EMA) said it has received a request from Merck to authorise its coronavirus antiviral, the first pill shown to treat Covid-19.

The EU drug regulator said in a statement, it had started evaluating molnupiravir, made by Merck and Ridgeback Biotherapeutics, and that a decision could be made within weeks on whether it might be cleared.

Last week, the EMA issued emergency advice saying that molnupiravir could be used to treat adults infected with the coronavirus who don’t yet need extra oxygen and are at increased risk of developing severe disease.

The agency said the drug should be given as soon as possible after Covid-19 has been diagnosed and within five days of symptoms starting.

It is intended to be taken twice a day for five days.

Watch | Covid-19: Are the new oral anti-viral pills effective?

Earlier this month, Britain became the first country in the world to approve the drug. The UK licensed molnupiravir for adults diagnosed with Covid-19 and with at least one risk factor for severe disease.

An antiviral pill that reduces symptoms and speeds recovery could prove groundbreaking, easing caseloads on hospitals and helping to curb explosive outbreaks in conjunction with vaccination campaigns.

Europe is now at the epicenter of the pandemic and the World Health Organisation has warned that without urgent measures, Europe could see 700,000 more Covid-19 deaths by the spring.

Molnupiravir is also pending review with regulators in the US, which is expected to convene an expert panel later this month to consider authorisation.

Even if the pill is licensed, initial supplies will be limited. Merck has said it can produce 10 million treatment courses this year, but much of that supply has already been purchased by governments worldwide.

In October, Merck agreed to let other drugmakers produce molnupiravir and signed a licensing agreement with the UN-backed Medicines Patent Pool allowing its pill to be made by companies in dozens of countries.

Published on November 24, 2021

Follow us on Telegram, Facebook, Twitter, Instagram, YouTube and Linkedin. You can also download our Android App or IOS App.

  1. Comments will be moderated by The Hindu Business Line editorial team.
  2. Comments that are abusive, personal, incendiary or irrelevant cannot be published.
  3. Please write complete sentences. Do not type comments in all capital letters, or in all lower case letters, or using abbreviated text. (example: u cannot substitute for you, d is not 'the', n is not 'and').
  4. We may remove hyperlinks within comments.
  5. Please use a genuine email ID and provide your name, to avoid rejection.

You May Also Like