Fampridine, which is approved to improve walking in MS patients, and Ocrevus may help ease walking impairments, a review of ...
Roche announced that the phase III MUSETTE trial comparing a high dose of Ocrevus (ocrelizumab) intravenous (IV ... a =20% increase in time to perform the timed 25-foot walk (T25FW); a =20% increase ...
Findings confirmed the approved 600mg IV dose was optimal for slowing disability progression in relapsing MS. A phase 3 study evaluating a higher dose of ocrelizumab in adults with relapsing ...
Roche (SIX: RO, ROG; OTCQX: RHHBY) announced today that the Phase III MUSETTE trial comparing a high dose of OCREVUS® (ocrelizumab) intravenous (IV) infusion to the currently approved OCREVUS IV 600 ...
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