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Final Analysis of Pivotal HOPE-B Study Demonstrates Durable and Sustained Therapeutic Effect of Etranacogene Dezaparvovec Gene Therapy in Hemophilia B - Data Presented at EAHAD 2022

KING OF PRUSSIA, Pa., Feb. 4, 2022 /PRNewswire/ Global biotherapeutics leader CSL Behring today announced positive long-term results from the P.

Vita cslbehringWolfgang miesbachEtranacogene dezaparvovecEuropean association of haemophiliaUniversity hospital of frankfurtHead of the department coagulation disordersCare centreEuropean associationAllied disordersProfessor wolfgang miesbachCoagulation disordersComprehensive care centreUniversity hospitalYear durability data fromHealthcare professionalsGene therapy

EMA Grants Accelerated Assessment for CSL Behring s Haemophilia B Gene Therapy

/PRNewswire/ CSL Behring today announced that the European Medicines Agency (EMA) has granted its approval for an accelerated assessment request for.

United statesVita cslbehringWolfgang miesbachKaren pinachyanFaraz kermaniEtranacogene dezaparvovecHead of medical affairs europeUniversity hospital of frankfurtEuropean unionEuropean medicines agencyDrug administrationMarketing authorisation applicationBreakthrough therapy designationUnited states foodPriority medicineLutz bonacker senior vice president

CSL Behring Receives Accelerated CHMP Assessment for Etranacogene Dezaparvovec for European Patients Living with Hemophilia B

/PRNewswire/ Global biotherapeutics leader CSL Behring today announced that the Committee for Medicinal Products for Human Use (CHMP), the chief scientific.

Vita cslbehringBrahm goldsteinEmmanuelle lecomte brissetEtranacogene dezaparvovecHead of global regulatory affairsEuropean medicines agencyCommittee for medicinal products human useMedicinal productsHuman useMarketing authorisation applicationGlobal regulatory affairsMarketing authorization applicationVice presidentLicense agreementGene therapyCsl behring

EMA Grants Accelerated Assessment for CSL Behring s Haemophilia B Gene Therapy

MARBURG, Germany, Dec. 15, 2021 /PRNewswire/ CSL Behring today announced that the European Medicines Agency (EMA) has granted its approval for an accelerated assessment request for etranacogene

United statesVita cslbehringWolfgang miesbachKaren pinachyanFaraz kermaniEtranacogene dezaparvovecHead of medical affairs europeUniversity hospital of frankfurtEuropean unionEuropean medicines agencyDrug administrationMarketing authorisation applicationBreakthrough therapy designationUnited states foodPriority medicineLutz bonacker senior vice president

CSL Behring Receives Accelerated CHMP Assessment for Etranacogene Dezaparvovec for European Patients Living with Hemophilia B

Press release content from PR Newswire. The AP news staff was not involved in its creation.

Vita cslbehringBrahm goldsteinEmmanuelle lecomte brissetEtranacogene dezaparvovecHead of global regulatory affairsEuropean medicines agencyCommittee for medicinal products human useMedicinal productsHuman useMarketing authorisation applicationGlobal regulatory affairsMarketing authorization applicationVice presidentLicense agreementGene therapyPr newswire

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