March 26 (Reuters) - Europe's drug regulator said on Friday
it had finished reviewing South Korean drugmaker Celltrion's
068270.KS COVID-19 antibody treatment, and found that while it
may lower hospitalisation rates, it could not reach a conclusion
on its benefits.
However, the treatment, regdanvimab, can be considered for
treating patients at high risk of getting severely ill, the
European Medicines Agency said, adding that a rolling review of
the treatment for European authorisation is still ongoing.
(Reporting by Pushkala Aripaka in Bengaluru; Editing by
Ramakrishnan M.)
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