Johnson & Johnson Submits First FDA Application for Nipocalimab to Treat Myasthenia Gravis (MG)

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Johnson & Johnson Submits First FDA Application for Nipocalimab to Treat Myasthenia Gravis (MG)

On August 29, 2024, Johnson & Johnson announced the submission of the first FDA application for nipocalimab, an investigational treatment targeting myasthenia gravis (MG).

Learn more in the full article here.

Myasthenia gravis (MG) is a neuromuscular disorder that causes muscle weakness, affecting the eyes, eyelids, facial expressions, chewing, swallowing, speaking, and other muscles.

Nipocalimab stands out as the first and only FcRn blocker designed to reduce autoantibodies, delivering sustained disease control. This was demonstrated through improvements in Activities of Daily Living for MG patients participating in the phase 3 Vivacity-MG3 study.

FcRn-targeted therapies for autoimmune diseases offer great potential. We are thrilled to provide a comprehensive range of human Fc gamma receptors and FcRn products to support your drug development research.

 

We also offer Cynomolgus/Rhesus/Macaque and mouse FcRn proteins from KACTUS:

Additionally, our portfolio includes anti-FcRn monoclonal and polyclonal antibodies from Proteintech, validated for IHC, WB, and ELISA. View them here.

Leverage our comprehensive FcRn and Fc gamma receptor products to advance your drug development research.

For more information, contact our support team at support@sanbio.nl.

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