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Urgently reviewing AstraZeneca COVID-19 vaccine trial data, says Britain medical regulator
UK: Britain's medical regulator said on Wednesday it is urgently reviewing information available to determine whether AstraZeneca AZN.L can restart trials of its experimental coronavirus vaccine after an unexplained illness in a participant.
In an email, director of licensing at the Medicines and Healthcare products Regulatory Agency (MHRA) Siu Ping Lam said the regulator is working with the Oxford Vaccine Centre to review the safety data, in line with protocol for the trial.
"We are urgently reviewing all the information and actively engaging with the researchers to determine whether the trial should restart as quickly as possible," he said.
Participant safety in any clinical trial is a top priority, he said. AstraZeneca is developing the potential vaccine with the University of Oxford.
Read also: Suspension of Covishield trials in UK spells havoc for Astrazeneca and Serum Institute of India
Ruchika Sharma joined Medical Dialogue as an Correspondent for the Business Section in 2019. She covers all the updates in the Pharmaceutical field, Policy, Insurance, Business Healthcare, Medical News, Health News, Pharma News, Healthcare and Investment. She has completed her B.Com from Delhi University and then pursued postgraduation in M.Com. She can be contacted at editorial@medicaldialogues.in Contact no. 011-43720751