EUSA Pharma
Manufacturing · United Kingdom · 201-500 Employees
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Overview
Headquarters
Breakspear Park Breakspear Way Ground Fl...Phone Number
+44 3305001140Website
www.eusapharma.comRevenue
$67.5 MillionIndustry
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EUSA Pharma News & Media
BeiGene and EUSA Pharma Announce China NMPA Approval of QARZIBA® (Dinutuximab Beta) for Patients with High-Risk Neuroblastoma
CAMBRIDGE, Mass. & BEIJING & HEMEL HEMPSTEAD, England--(BUSINESS WIRE)---- $BGNE #BTKi--BeiGene, Ltd. (NASDAQ: BGNE; HKEX: 06160) and EUSA Pharma (UK), Ltd. today announced that the China National Medical Products Administration (NMPA) has granted QARZIBA® (dinutuximab beta) conditional approval for the treatment of high-risk neuroblastoma in patients aged 12 months and above who have previously received induction chemotherapy and achieved at least a partial response, followed by myeloablative tSYLVANT® (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
HEMEL HEMPSTEAD, England & BURLINGTON, Mass.--(BUSINESS WIRE)--EUSA Pharma (UK) Limited (“EUSA Pharma”), a global biopharmaceutical company focused on oncology and rare diseases, announced that the National Comprehensive Cancer Network® (NCCN®) has updated their Clinical Practice Guidelines in Oncology (NCCN Guidelines®) for B-Cell Lymphomas to include siltuximab (SYLVANT®) as the preferred primary treatment for patients with human immunodeficiency virus–negative [HIV(-)] and human herpesvirusEUSA Pharma and BeiGene Announce Acceptance of a Biologics License Application for SYLVANT® (Siltuximab for Injection) in China
HEMEL HEMPSTEAD, England & BEIJING, China & CAMBRIDGE, Mass.--(BUSINESS WIRE)--EUSA Pharma (UK) Limited and BeiGene, Ltd. (NASDAQ: BGNE; HKEX: 06160) today announced that the Biologics License Application (BLA) for SYLVANT® (siltuximab for injection) was accepted by the China National Medical Products Administration (NMPA) and granted priority review. Siltuximab is a monoclonal antibody approved by the European Medicines Agency (EMA) and Food and Drug Administration (FDA) for the treatment of aEUSA Pharma annonce le recrutement du premier patient dans un essai clinique randomisé de Phase 3 portant sur le siltuximab chez des patients hospitalisés atteints de COVID-19 ou d'un autre syndrome de détresse respiratoire aiguë (SDRA) associé à...
HEMEL HEMPSTEAD, Royaume-Uni & BURLINGTON, Massachusetts--(BUSINESS WIRE)-- EUSA Pharma annonce le recrutement du premier patient dans un essai clinique randomisé de Phase 3 portant sur le siltuximab chez des patients hospitalisés atteints de COVID-19 ou d'un autre syndrome de détresse respiratoire aiguë (SDRA) associé à une infection respiratoire virale EUSA Pharma (UK) Limited ("EUSA Pharma"), une société biopharmaceutique mondiale, a annoncé aujourd'hui le recrutement d'un premier patient d
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Frequently Asked Questions Regarding EUSA Pharma
Founded in 1985, EUSA Pharma is a pharmaceutical company focused on oncology and rare disease. EUSA Pharma is located in the United Kingdom... Read More