Roche's Actemra finding a place in COVID-19 armamentarium
The US regulator has accepted a supplemental Biologics License Application (sBLA) for Actemra (tocilizumab), granting the intravenously-administered product Priority Review.
Swiss cancer giant Roche (ROG: SIX) is bidding for approval to market the product, which is sold under the RoActemra brand in Europe, for the treatment of COVID-19 in certain hospitalized adults.
In some parts of the world, vaccination rates are still lower than hoped, leaving open the prospect of continued waves of coronavirus infections, with many ending up in hospital.
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