Yes, inebilizumab (brand name: Uplizna) is FDA approved. The U.S. Food and Drug Administration (FDA) approved inebilizumab on June 11, 2020.
Inebilizumab is an intravenous medication used to treat neuromyelitis optica spectrum disorder (NMOSD) in adults who are positive for the anti-aquaporin-4 (AQP4) antibody. NMOSD, also known as Devic's disease, is a central nervous system disorder where the immune system attacks the optic nerves and spinal cord, leading to symptoms such as vision loss, paralysis, and severe pain.
Inebilizumab is a monoclonal antibody that selectively targets and depletes B cells expressing CD19. By reducing the number of these B cells, inebilizumab helps to lower the risk of relapses and manage the symptoms of NMOSD.
Inebilizumab is administered via intravenous infusion. The initial treatment consists of two 300 mg infusions given two weeks apart. After the initial doses, a maintenance dose of 300 mg is administered every six months.
Pre-treatment and Monitoring:
Precautions and Considerations
Before Treatment:
Pregnancy and Breastfeeding:
Common Side Effects:
Serious Side Effects:
Patients should report any new or worsening symptoms to their healthcare provider immediately.
Inebilizumab, marketed as Uplizna, is an FDA-approved treatment for NMOSD, helping to reduce relapses and manage symptoms in affected individuals. Approved on June 11, 2020, it offers a new option for patients with this debilitating condition.
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