EU Regulator To Decide On Pfizer/BioNTech Covid-19 Jab First
Sumaira FH 2 months ago Tue 01st December 2020 | 06:40 PM
Frankfurt am Main, Dec 1 (UrduPoint / Pakistan Point News - 1st Dec, 2020 ) :Europe's medicines regulator said Tuesday it would decide by December 29 whether to grant emergency approval to a Covid-19 vaccine developed by Germany's BioNTech and its US partner Pfizer, ahead of a rival treatment from Moderna.
The European Medicines Agency (EMA) confirmed that it had received formal applications from both vaccine makers seeking the green light for their experimental jabs.
"If the data submitted are robust enough to conclude on the quality, safety and effectiveness of the vaccine," the Amsterdam-based agency said it could conclude its assessment of the BioNTech/Pfizer shot in an extraordinary meeting on 29 December "at the latest".
A separate meeting to assess the Moderna shot would take place on January 12 at the latest, it added.
Large-scale trial data released last month showed that both vaccines were safe and around 95 percent effective against Covid-19.
European Commission spokesman Stefan de Keersmaecker told reporters that once the EMA had given regulatory permission, formal authorisation from Brussels would follow "very quickly", probably "in a matter of days".
Although both vaccines are being assessed in an accelerated process known as a "rolling review", the latest timeline suggests Europeans would be lucky to receive the first jabs before the year is over.
BioNTech/Pfizer and Moderna have also applied for emergency use authorisation in the United States, where Americans are expected to start getting vaccinated around mid-December.
UK regulators, who because of Brexit no longer have to wait for the EMA's okay, are also in the process of considering emergency approval of the BioNTech/Pfizer vaccine.
- 'Ready to ship' - BioNTech and Pfizer said they had asked the EMA for "conditional market approval" (CMA) of their vaccine on Monday, after filing a request for emergency authorisation in the US on November 20.
"We have known since the beginning of this journey that patients are waiting, and we stand ready to ship Covid-19 vaccine doses as soon as potential authorisations will allow us," Pfizer CEO Albert Bourla said.
A CMA can be granted "in emergency situations in response to public health threats", the EMA says on its website.
Fellow vaccine frontrunner Moderna, a US biotech firm, meanwhile said it had sought emergency approval for its Covid-19 shot in both the US and Europe on Monday.
The BioNTech/Pfizer and Moderna vaccines have been developed at breathtaking speed as part of an unprecedented effort to end a pandemic that has killed more than 1.4 million people worldwide and devastated the global economy.
No mRNA vaccines have ever been approved for widespread use.
- Highly effective - As well as proving highly effective in preventing Covid-19, both vaccines were found to be consistent across all age-groups -- a Primary concern for a disease that hits the elderly the hardest -- as well as genders and ethnicities.
But there are important differences between the two.
Moderna's vaccine can be kept in long-term storage at minus 20 degrees Celsius (minus four degrees Fahrenheit) while Pfizer's requires minus 70 degrees Celsius (minus 94 degrees Fahrenheit).
On the other hand, the Pfizer/BioNTech doses are much smaller -- 30 micrograms to Moderna's 100 micrograms -- probably lowering production costs per dose.
It remains unclear how long exactly protection against Covid-19 might last, and both vaccines will likely require a booster shot.
Moderna has said it aims to have approximately 20 million doses of its vaccine, called mRNA-1273, available in the US by the end of the year.
According to the World Health Organization, around 100 vaccine candidates are currently in development. Around a dozen of them are in the final phase three stage when the shot is tested on tens of thousands of volunteers.