BeiGene gains approval for Sylvant in China
The China National Medical Products Administration (NMPA) has approved Sylvant (siltuximab for injection) for the treatment of adult patients with multicentric Castleman disease (MCD) who are human immunodeficiency virus (HIV) negative and human herpes virus-8 (HHV-8) negative, also known as idiopathic MCD (iMCD).
Sylvant was licensed to BeiGene (HKEX: 06160) by UK-based drugmaker EUSA Pharma in January last year, granting exclusive rights to the drug in China, Hong Kong, Macau, and Taiwan. The deal is worth a potential $160 million to the UK firm.
This disease is a rare, life-threatening, and debilitating condition of the lymph nodes and related tissues. Siltuximab is a monoclonal antibody approved in the USA, European Union, and other countries and regions around the world.
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