This medication requires a valid prescription. Please refer to the ‘Prescription Guide’ for details.

Uplizna (inebilizumab-cdon)

General Description

Uplizna (inebilizumab-cdon) is prescribed for adults with neuromyelitis optica spectrum disorder (NMOSD) who test positive for anti-aquaporin-4 (AQP4) antibodies.

It is the first approved treatment for NMOSD that is administered just twice a year.

Getting Uplizna (inebilizumab-cdon) in India

Uplizna (inebilizumab-cdon) is approved in the U.S., Europe, and other countries, but it is not yet commercially available in India. However, eligible patients in India may access this important therapy through the Named Patient Program (NPP).

MitoGENE helps patients obtain Uplizna (inebilizumab-cdon) legally and safely, in collaboration with their treating doctor. We assist with documentation, import coordination, and delivery—ensuring full compliance with Indian regulatory guidelines.

If you or a loved one needs Uplizna (inebilizumab-cdon), MitoGENE is here to guide you through every step of the process.


Disease Indications:Neuromyelitis Optica Spectrum Disorder

Manufacturer:Viela Bio

Usage:Intravenous

Medicine Approved by:

  • U.S. Food and Drug Administration (FDA)

Available Dosage Form & Package:

  • 3 Single dose vials 100mg/10ml

Shipping:Cold Chain Shipping. Certain medicines can be affected by heat, light, or improper handling. Cold chain shipping uses temperature-controlled packaging and transport provided by specialized medical couriers to keep these medicines stable and effective. Due to the added care and equipment involved, this method is often more expensive than standard shipping.

What is Uplizna (inebilizumab-cdon) used for?

Uplizna (inebilizumab-cdon) is a CD19-targeting monoclonal antibody used to treat neuromyelitis optica spectrum disorder (NMOSD) in adults who test positive for anti-aquaporin-4 (AQP4) antibodies.[1]
It comes in a single-dose vial containing 100 mg/10 mL of inebilizumab-cdon.[1]


How does Uplizna work?

NMOSD is a rare autoimmune condition of the central nervous system where the immune system attacks healthy nerve cells, particularly those expressing the aquaporin-4 (AQP4) protein. This can lead to damage in the optic nerves, spinal cord, and brain.[2]

Uplizna is a type of immunotherapy known as a monoclonal antibody, designed to bind to CD19, a protein found on B cells (a type of white blood cell). B cells are believed to play a significant role in the disease process of NMOSD.[3]
Once in the bloodstream, Uplizna attaches to CD19 on B cells and triggers their destruction, thereby helping to reduce disease activity.[3]


Where is Uplizna approved?

Uplizna was approved by the U.S. Food and Drug Administration (FDA) on June 11, 2020, for adults with NMOSD who are anti-AQP4 antibody positive.[2]
The FDA has also granted UpliznaBreakthrough Therapy and Orphan Drug designations.[2]

It may also be approved in other countries or regions. Please contact our support team if you need details on its availability in a specific country.


How is Uplizna administered?

The recommended treatment schedule includes:[1]

  • Initial phase: 300 mg IV infusion, followed two weeks later by another 300 mg IV infusion
  • Maintenance: Starting six months after the first dose, a single 300 mg IV infusion every six months

Before starting Uplizna, patients should undergo screening for infections like hepatitis B and tuberculosis.
Any necessary vaccinations should be administered at least 4 weeks prior to the first infusion.[1]

Before each dose, patients should be checked for active infections. If an infection is present, treatment should be postponed until recovery.[1]

Premedication may be given prior to each infusion to reduce the risk of infusion-related side effects.[1]
For full dosing and administration details, refer to the official prescribing information.[1]

Important: Always consult your treating physician for personalized medical guidance.


What are the possible side effects of Uplizna?

Common side effects (≥10% of patients) may include:[1]

  • Urinary tract infections (UTIs)
  • Joint pain (arthralgia)

Serious side effects listed include:[1]

  • Infusion-related reactions
  • Reactivation of Hepatitis B
  • Progressive multifocal leukoencephalopathy (PML), a rare brain infection
  • Tuberculosis (TB)

Use in Special Populations

Uplizna may cause harm to the fetus if used during pregnancy. It is advised to avoid pregnancy and breastfeeding while on this medication.[1]

For a detailed list of potential side effects, please consult the official prescribing information.[1]

References

1. Full prescribing information [FDA]: Uplizna (inebilizumab-cdon) [PDF]
Viela Bio, Jun 2020

2. Viela Bio Announces U.S. FDA Approval of UPLIZNA™ (inebilizumab-cdon) for the Treatment of Neuromyelitis Optica Spectrum Disorder (NMOSD)
Globe News Wire press release, June 11, 2020

3. B cell-based therapies in CNS autoimmunity: differentiating CD19 and CD20 as therapeutic targets
Forsthuber TG, Ther Adv NeurolDisord, Mar 21, 2018

How to Access Uplizna (inebilizumab-cdon) in India in 4 Simple Steps with MitoGENE via the Named Patient Program (NPP)

If Uplizna (inebilizumab-cdon) is not yet approved or available commercially in India, MitoGENE can help you access it through a legal pathway. Here’s how: