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Salud.Moderna ensures that its vaccine against Covid-19 activates a strong immunity in older people
Covid-19: the latest advances in 'anticovid' vaccines
Closer.
While an adverse effect puts Johnson & Johnson trials on hold, Moderna has
submitted the 'papers' to formally request the approval
of its candidate in Europe.
In this way, the European Medicines Agency (EMA) will be able to evaluate the mRNA-1273 vaccine in order to request a marketing authorization from the European Union.
In this sense, the EMA's confirmation highlights Moderna's commitment to make the vaccine
accessible to the entire European Union
.
Moderna's request for authorization will include
updated clinical information on mRNA-1273
.
It includes the results obtained from a preclinical study on the virus, as well as the provisional analysis of Phase 1 of the study of mRNA-1273 in adults (18-55 years) and the elderly (56-70 and 71+ years ) published in the
New England Journal of Medicine
.
In this trial, results in
older
people
showed that the vaccine produces neutralizing antibodies to
the virus at levels similar to those seen in younger adults, with side effects roughly on par with flu vaccines.
In Europe, the company is working with its strategic partners, the Swiss, Lonza, and the Spanish, ROVI, to manufacture and supply the vaccine.
It is a supply chain dedicated entirely to supporting Europe and countries that, apart from the United States, have purchasing agreements with Moderna.
Thus, a total of 22,194 participants of the COVE phase IIO study of the candidate vaccine, mRNA-1273, have received the second dose of the vaccine as of October 9.
On the other hand, Moderna announced yesterday that the Canadian Ministry of Health will begin the evaluation of its candidate.
To date, this candidate has had no serious adverse problems.
In the
New England
,
mild side effects,
including headache, fatigue, body aches, chills, and injection site pain, were rated as mild to moderate.
However, in at least two cases, the volunteers had severe reactions.
One developed a grade three fever, which is classified as 39 ° C or higher, after receiving the lowest dose of the vaccine.
Another developed such severe fatigue that it temporarily prevented daily activities.
Side effects usually occurred shortly after receiving the vaccine and resolved quickly.
According to the criteria of The Trust Project
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