A 10-minute subcutaneous formulation of Roche’s multiple sclerosis (MS) blockbuster Ocrevus (ocrelizumab) could be a convenient alternative to a two-hour intravenous infusion and could expand access for patients for whom it is difficult to reach an infusion center. The US Food and Drug Administration approved Ocrevus Zunovo (ocrelizumab and hyaluronidase) on 13 September.
Key Takeaways
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The US FDA approved a new subcutaneously administered version of Roche’s blockbuster multiple sclerosis drug Ocrevus.
The two formulations will be priced the same, though a subcutaneous administration can avoid some administration costs. Because the molecules...
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