CHICAGO/WASHINGTON: AstraZeneca's COVID-19 vaccine trial in the United States is expected to resume as early as this week after the US Food and Drug Administration completed its review of a serious illness, four sources told Reuters.
Regulators in Brazil, India and South Africa also previously allowed AstraZeneca to resume its vaccine trials there. Vaccines are seen as essential to helping end the pandemic that has battered economies around the world and claimed more than 1 million lives - over 220,000 of them in the United States.
The Health Research Authority, which helps oversee UK medical research, said in an email to Reuters that it vetted the communication to make sure it was suitable to ensure informed consent among study volunteers. It could not confirm that the letter had been issued. Dr Paul Offit, director of the Vaccine Education Center at Children’s Hospital of Philadelphia who reviewed the document, said it can be difficult to link a rare side effect specifically to a vaccine to the exclusion of other potential causes.
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