FDA Approves Subcutaneous Ocrevus for Multiple Sclerosis Treatment
Overview of Ocrevus Zunovo
Ocrevus Zunovo (ocrelizumab and hyaluronidase-ocsq) is now approved for treating relapsing multiple sclerosis (RMS) and primary progressive multiple sclerosis (PPMS). This subcutaneous formulation enables approximately 10-minute injections by healthcare providers every six months.
Significance of FDA Approval
This approval marks a significant step forward in multiple sclerosis treatment options. “People are living longer with chronic illnesses and with fewer disabilities...” states Natalie Blake, executive director of the MS Foundation, highlighting the need for accessible medicine.
Clinical Insights
- Ocrevus Zunovo is built on a successful intravenous product design.
- Targets CD20-positive B cells to mitigate myelin damage.
- Annual cost of Ocrevus is currently $78,858.
Efficacy and Patient Feedback
Clinical trials exhibited 97% suppression of relapse activity and positive feedback from participants on the injection method. More than 92% reported satisfaction with subcutaneous administration.
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