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Sanofi reveals detailed timeframe for RSV candidate

Now that a new set of study data supports a possible treatment for RSV, Sanofi has laid out its plan for applying to regulatory authorities.

Photo: CHARLES PLATIAU/Reuters / X00217

Over the course of the first six months of 2022, Sanofi expects to submit the first regulatory application for marketing authorization for a possible treatment of respiratory syncytial virus (RSV) in infants.

In a press release, the company states that it has received results from a phase II/III trial of the drug nirsevimab, which supports the drug candidate.

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