Moderna says it will request US, Europe vaccine authorisation

File: The manufacturing will be backed financially by Japan as well as the US International Development Finance Cooperation, which provides funding for projects in developing countries. Hendrik Schmidt / POOL / AFP

WASHINGTON - US firm Moderna said it would file requests for emergency authorisation of its COVID-19 vaccine in the United States and Europe on Monday after full results confirmed a high efficacy estimated at 94.1 percent.

"We believe that our vaccine will provide a new and powerful tool that may change the course of this pandemic and help prevent severe disease, hospitalisations and death," said the company's CEO Stephane Bancel.

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If the US Food and Drug Administration agrees it is safe and effective, the first of the drug's two doses could be injected into the arms of millions of Americans by the middle of December. 

American pharmaceutical Pfizer and Germany's BioNTech applied for similar approvals last week, and their vaccine could be greenlit in the US shortly after December 10.

The Moderna vaccine, which was co-developed with the US National Institutes of Health, is being studied in a clinical trial with more than 30,000 participants across the United States.

An interim analysis announced earlier this month was based on 95 patients who fell sick with COVID-19.

The final analysis was based on 196 cases, 185 of which were observed in a group assigned a placebo versus 11 who received the shots.

Thirty people had severe cases -- all of whom were in the placebo group -- which also included one person who died.

Significantly, efficacy was uniform across age, race, ethnicity and gender, the company said. 

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The 196 Covid-19 cases included 33 adults over the age of 65, and 42 participants identifying as being from diverse communities (including 29 Hispanic, six Black, four Asian Americans and three multiracial participants).

The vaccine was generally well tolerated, with the most common side effects including injection site pain, fatigue, muscle pain, joint pain, headache, and redness at the site.

These increased in frequency and severity after the second dose in the vaccinated group.

The press statement included the line: "no new serious safety concerns have been identified by the Company" -- but it did not explicitly say whether serious concerns have been flagged previously.

Moderna said it expects to have approximately 20 million doses of the vaccine, called mRNA-1273, available in the US by the end of the year.

It also expects to manufacture 500 million to 1 billion doses globally in 2021.

 

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Source
AFP

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