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BeiGene and EUSA Pharma Announce NMPA Approval of SYLVANT^® (Siltuximab for Injection) in China for Idiopathic Multicentric Castleman Disease

BeiGene and EUSA Pharma Announce China NMPA Approval of QARZIBA^® (Dinutuximab Beta) for Patients with High-Risk Neuroblastoma

EUSA Pharma Announces Appointment of Carsten Thiel as New Chief Executive Officer

SYLVANT^® (siltuximab) Recommended by the National Comprehensive Cancer Network^® (NCCN^®) as the Preferred Treatment Option for Patients with Idiopathic Multicentric Castleman Disease (iMCD) regardless of histopathologic subtype

EUSA Pharma and BeiGene Announce Acceptance of a Biologics License Application for SYLVANT^® (Siltuximab for Injection) in China

EUSA Pharma To Present at the 39th Annual J.P. Morgan Healthcare Conference

EUSA Pharma Announces First Patient Enrolled in a Randomised Phase 3 Clinical Trial Investigating Siltuximab in Hospitalised Patients with COVID-19- or Another Respiratory Virus Infection-Associated Acute Respiratory Distress Syndrome (ARDS)

EUSA Pharma and BeiGene Announce Acceptance of a Biologics License Application for QARZIBA^®▼ (Dinutuximab Beta) in China

EUSA Pharma are proud to be featured in this year’s Sunday Times Sage Tech Track 100

EUSA Pharma are proud to be featured in this year’s Sunday Times Sage Tech Track 100 as one of Britain’s private technology companies with the fastest-growing sales.

EUSA Pharma Announces FDA Approval of Phase 3 Clinical Trial for Siltuximab in Hospitalized Patients with COVID-19 Associated Acute Respiratory Distress Syndrome