Roche says REMDACTA trial misses in severe COVID-19 pneumonia
Roche (ROG: SIX) today revealed that the global Phase III randomized, double-blind, multicenter REMDACTA study of Actemra/RoActemra (tocilizumab) plus Veklury (remdesivir), versus placebo plus Veklury, did not meet its primary endpoint.
This was measured by improved time to hospital discharge up to day 28 in patients with severe COVID-19 pneumonia receiving standard of care. No new safety signals were identified for Actemra/RoActemra in the REMDACTA trial, the Swiss pharma giant said.
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