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The following is a summary of “Recall vaccination increases detectable B-cell reactivity in persons with multiple sclerosis treated with ocrelizumab,” published in the April 2025 issue of Journal of ...
One in three women diagnosed with MS will subsequently conceive, therefore consideration of the maternal-infant dyad is ...
The findings indicate that the currently approved 600-mg dose of intravenous ocrelizumab is optimal to significantly slow ...
In the Phase III MUSETTE study, a higher dose of intravenous Ocrevus (ocrelizumab) did not provide additional benefit in ...
Two prominent scientists who study multiple sclerosis — Dr. Alberto Ascherio and Dr. Stephen Hauser — are co-winners of a ...
Neuro-immunologist Stephen Hauser , MD, whose maverick thinking transformed the treatment landscape for patients with ...
No added benefits in slowing MS disability progression were found in a study that increased Ocrevus dosing to 2-3 times the ...
The study aimed to determine whether treatment with high dose ocrelizumab would provide an additional benefit in slowing disability progression.
Roche’s phase III MUSETTE trial of Ocrevus high dose in people with relapsing multiple sclerosis fails to meet primary endpoint: Basel Friday, April 4, 2025, 11:00 Hrs [IST] Roc ...
Higher doses of the company’s intravenously delivered multiple sclerosis drug failed to show additional benefit in slowing ...
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 ...
Roche Holdings AG (OTC:RHHBY) on Wednesday announced data from MUSETTE Phase 3 trial of a high dose of Ocrevus (ocrelizumab) ...
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