EMA official says COVID-19 vaccine could be approved in a year.

CV-19 origin evidence under scrutiny


An EMA official says COVID-19 vaccine could be approved in a year.

A vaccine against SARS-CoV-2, the novel coronavirus scourging the globe, could be approved in the European Union in about a year, Marco Cavaleri, the European Medicines Agency’s top official overseeing anti-infectives and vaccines, reports.

Cavaleri cautioned that this is an optimistic view but said the ambition is to have a vaccine approved next Spring and that he is skeptical of claims that a vaccine could be ready by September.

“I have to stress that this is a best-case scenario,” he said during a virtual press conference, noting that not all development efforts will bear fruit, and there is always the potential for unforeseen delays.

Further Trials

Cavaleri also said that EMA expects all vaccines to prevent coronavirus disease (COVID-19) will be studied in large Phase 3 trials before approval and noted that EMA would be open to reviewing data from challenge studies, where volunteers are intentionally infected with the virus, if such studies were found to be ethical.

“As regulators, we are going to be very careful in having a good assessment of the safety and efficacy of these vaccines, and therefore we will not be cutting corners,” he said.

For drugs, approval could come sooner as many products being studied to treat COVID-19 are already approved for other indications or have been studied in humans for other conditions.

“It might be possible that before the summer, some of these therapeutics could be approved,” Cavaleri said, noting that we have already seen topline trial results for some products. Earlier this month, EMA announced it had started a rolling review of Gilead Sciences’ remdesivir after preliminary results from a US study found patients taking the drug recovered faster than those on placebo.

EMA Coalition

Cavaleri emphasised that EMA has been working closely with other regulators through the International Coalition of Medicines Regulatory Authorities (ICMRA) to ensure alignment on regulatory expectations for drugs and vaccines for COVID-19.

“This is very important because we all recognise the importance in being aligned in the requirements and what we can do in order to speed up the development of vaccines and therapeutics in the context of COVID-19,” he said.

EMA has been in contact with developers regarding roughly 115 therapeutics and 33 vaccines, according to Marie-Agnes Heine, Head of Communications at the agency.

CV-19 Vaccine Research Data – A Hacker’s Legacy!

The race to develop a vaccine is particularly high stakes. While many countries claim they’re willing to collaborate internationally throughout the process, it’s unsurprising that some nations would turn to espionage to fill the gaps and suss out what researchers might be holding back. But if these operations disrupt or damage vaccine development, they could violate the norms surrounding espionage. A joint statement by the Federal Bureau of Investigation and the Department of Homeland Security’s Cybersecurity and Infrastructure Security Agency accuses China of doing exactly that.


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