An earlier than expected and positive read-out of a Phase III trial of AstraZeneca PLC and Sanofi’s nirsevimab puts the firms firmly in prime position to shake up the substantial and as yet mostly untapped respiratory syncytial virus (RSV) market.
Top-line data from the MELODY study show that the passive immunotherapy met its primary endpoint of a reduction in the incidence of medically attended lower respiratory tract infections (LRTI) caused by RSV through 150 days after a single dose compared with placebo in healthy late preterm and term infants (35 weeks or more)
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