Pence will get the shot during a White House event to “build confidence among the American people,” his office said in a statement.
Many are taking up the offer. Called “the Vaccine Transition Option,” the effort allows trial participants who got the placebo to receive the real two-dose regimen, while continuing to be monitored by investigators.
Rich countries with less than 15% of the global population have reserved 51% of the doses of the most promising vaccines, researchers said on Tuesday.
The school closure is a step towards the imposition of Phase 3 social distancing rules, a move that would essentially lock down Asia's fourth-largest economy.
Despite months of preparation, distributing and administering the vaccine to as many as 330 million recipients poses a major logistical challenge, he said. The vaccine has complex shipping requirements and must be stored at -70 Celsius.
The first vaccine was approved late on Friday by the US Food and Drug Administration and is expected to touch off a mass-inoculation campaign of unparalleled dimension to end the pandemic that has upended daily life and devastated the U.S. economy.
The Centers for Disease Control and Prevention has not yet endorsed the vaccine for pregnant women, but an advisory committee to the agency is expected to meet this weekend to make further recommendations.
In a 17-4 vote with one abstention, the government advisers on Thursday concluded that the vaccine from Pfizer and its German partner BioNTech appears safe and effective for emergency use in adults and teenagers 16 and older.
The researchers from Alagappa University in Tamil Nadu and KTH Royal Institute of Technology, Sweden propose a list of individual drugs and cocktails that deserve testing for the treatment of COVID-19.
Chief Minister Yogi Adityanath set December 15 deadline to increase the storage capacity. The chief minister has also directed officials to prepare the Covid vaccine cold chains on the lines of pulse polio vaccine cold chains, and ensure strict security at the centres.
Pfizer has said people with a history of severe adverse allergic reactions to vaccines or the candidate's ingredients were excluded from their late stage trials, which is reflected in the MHRA's emergency approval protocol.
Pfizer and BioNTech said they did not believe any personal data of trial participants had been compromised and EMA "has assured us that the cyber attack will have no impact on the timeline for its review."
The Oxford-AstraZeneca effort held great promise to help arrest the pandemic. But a series of miscues caused it to fall behind in the U.S.
While the efficacy rate may be enough to get the vaccine approved, the variability in different subgroups and lack of data for older people should give regulators pause in rushing this through, according to a Bloomberg Intelligence analyst.
The first recipient was grandmother Margaret Keenan, who turns 91 next week. She received the shot at University Hospital Coventry at 6:31 a.m.
The pandemic has shown humanity at "its best and worst," he said, pointing to "inspiring acts of compassion and self-sacrifice, breathtaking feats of science and innovation, and heartwarming demonstrations of solidarity, but also disturbing signs of self-interest, blame-shifting and divisions."
The specter of Britain beating the United States to approval — on a vaccine co-developed by an American company, at that — may intensify pressure on US regulators, who are already under fire from the White House for not moving faster to get doses to people.
While the first confirmed case of COVID-19 in the US was identified on January 19, 2020, the scientists noted that antibodies reactive against the coronavirus were detected in 106 of the 7,389 specimens.
Reports of a mysterious pneumonia spreading in Wuhan, China, first emerged in late December 2019.
Amritsar is one of the worst affected, Tarn Taran among the least; govt officials attribute it to urban-rural divide.
The filing sets Moderna's product up to be the second vaccine likely to receive US emergency use authorisation this year.
Clearance is possible as soon as early next week, according to a person familiar with the situation. British doctors were put on standby for a possible rollout before Christmas.
Questions are mounting over one of the fastest-moving shots after the company acknowledged that a lower dosage level that appeared more effective resulted from a manufacturing discrepancy.
Health Canada had said previously that an approval would likely come early in the first quarter, under a new accelerated review process very similar to that in place in the United States.
Brazil has the second highest number of coronavirus deaths in the world, and Bolsonaro has for months played down the seriousness of the pandemic despite being infected with the virus in July.

