Alnylam’s zilebesiran met the primary endpoint and certain secondary endpoints in a Phase II dose-ranging trial in a readout that arrived less than six weeks after Roche announced it would pay $310 million to co-develop and co-commercialize the therapy.
Alnylam revealed topline data Thursday from the KARDIA-1 trial, which enrolled 394 patients across five arms and tested zilebesiran as a monotherapy in adults with mild to moderate hypertension.
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