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BeiGene Files China BLA for Sylvant, a Rare Disease Therapy

publication date: Jan 27, 2021

BeiGene and the UK's EUSA Pharma announced that their Sylvant® BLA was accepted for Priority Review in China. Sylvant is a treatment for adult patients with multicentric Castleman’s disease (MCD). A rare disease, MCD is a debilitating condition of the lymph nodes and related tissues. One year ago, BeiGene acquired Greater China commercialization rights to Sylvant from EUSA as part of a $160 million two-drug in-licensing agreement. More details....

Stock Symbols: (NSDQ: BGNE; HK: 06160)

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