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Description
Participants, ages 18-65 and with a disease duration of up to 15 years, were randomly assigned to receive an initial 920 mg dose of the subcutaneous formulation or the approved 600 mg dose of Ocrevus, which is given initially in two intravenous infusions two weeks apart
E.VisheM.TukachinskyH.ZhengS.-L.LiF.et al (2022)
Allow them to dry completely before proceeding
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