Federal health regulators have decided to allow the resumption of U.S. studies of a leading Covid-19 vaccine candidate from AstraZeneca PLC and the University of Oxford, according to a person familiar with the matter and materials reviewed by The Wall Street Journal.examination of two cases of a possible neurological side effect
that emerged in two people testing the shot. The agency told AstraZeneca on Friday that the late-stage trial in the U.S. can resume, according to the person and materials. The FDA didn’t find the vaccine was responsible for the two cases, though it couldn’t rule out a link either, the person said. The agency plans to require researchers to inform study subjects of the cases and monitor them for any related neurological events, such as numbness, the person said.
AstraZeneca declined to comment. An FDA spokeswoman didn’t immediately respond to a request for comment.
DrOz
‘According the the person familiar with the matter ‘...alright then.
Convenient pump
So who wants to die next?
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