Pfizer and BioNTech said they plan to submit the data to other
regulatory agencies around the world.
Final results from
Pfizer's Covid-19 vaccine trial showed its shot had a 95 per cent success rate
and two months of safety data, paving the way for the drugmaker to apply for an
emergency US authorisation within days, it said on Wednesday. Pfizer said it
expected the US FDA vaccine advisory committee to review and discuss the data
in a public meeting that will likely be held in December.
The efficacy rate
of the vaccine, developed by Pfizer
and its German partner BioNTech, is the highest of any candidate in late-stage
clinical trials so far. Global shares edged higher on Wednesday as Pfizer's
trial results more than offset concerns around the stubbornly high global
infection rate. Pfizer shares rose 2.9 per cent when US markets opened while
BioNTech jumped 4 per cent.
Pfizer has said it
is exploring possibilities to make the Covid-19 vaccine available in India.
“The firm remains committed to engaging with the government of India to advance
its dialogue and explore opportunities to make the vaccine available for use in
India,” it said.
Pfizer and BioNTech
said they plan to submit the data to other regulatory agencies around the
world.
V K Paul,
member-health, NITI Aayog, and also the chairman of the committee on vaccine
administration, said: “The vaccine needs to be kept in -70-degree Celsius
temperature and will be difficult for countries to scale up... We are
discussing this. The Pfizer vaccine will not be available to us for a few months.”
The government is examining all possibilities to extend cold-chain facilities
in case Pfizer is procured.
No comments:
Post a Comment