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HEALTH-VIRUS-VACCINE-MODERNA
Moderna says will request US, Europe vaccine authorization Monday
WASHINGTON, Nov 30, 2020 (BSS/AFP) – US firm Moderna said it would file
requests for emergency authorization 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,
hospitalizations and death,” said the company’s CEO Stephane Bancel.
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.
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.
BSS/AFP/FI/ 1920 hrs