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    [{"orgOrder":0,"company":"LFB","sponsor":"HEMA Biologics","pharmaFlowCategory":"DU","amount":"Not Applicable","upfrontCash":"Not Applicable","newsHeadline":"LFB Announces FDA Approval of SEVENFACT for the Treatment of Adults and Adolescents with Hemophilia A or B with Inhibitors","therapeuticArea":"Genetic Disease","highestDevelopmentStatus":"Approved","country":"FRANCE","productType":"Large molecule","productStatus":"Approved","date":"April 2020","url1":"","url2":"","graph1":"Genetic Disease","graph2":"Approved"},{"orgOrder":0,"company":"LFB","sponsor":"Not Applicable","pharmaFlowCategory":"DU","amount":"Not Applicable","upfrontCash":"Not Applicable","newsHeadline":"CHMP Recommends Cevenfacta to Control Bleeding Episodes in Patients With Congenital Haemophilia","therapeuticArea":"Genetic Disease","highestDevelopmentStatus":"Approved","country":"FRANCE","productType":"Large molecule","productStatus":"Approved","date":"May 2022","url1":"","url2":"","graph1":"Genetic Disease","graph2":"Approved"},{"orgOrder":0,"company":"LFB","sponsor":"Not Applicable","pharmaFlowCategory":"DU","amount":"Not Applicable","upfrontCash":"Not Applicable","newsHeadline":"LFB Announces the Approval of CEVENFACTA\u00ae (eptacog beta) in the European Union","therapeuticArea":"Genetic Disease","highestDevelopmentStatus":"Approved","country":"FRANCE","productType":"Large molecule","productStatus":"Approved","date":"July 2022","url1":"","url2":"","graph1":"Genetic Disease","graph2":"Approved"}]

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              LFB Announces the Approval of CEVENFACTA® (eptacog beta) in the European Union

              Details:

              Cevenfacta (eptacog beta), a new recombinant coagulation Factor VIIa for treatment of bleeding episodes and for prevention of bleeding in those undergoing surgery or invasive procedures in adults and adolescents with haemophilia A or B with inhibitors.

              Lead Product(s): Eptacog Beta

              Therapeutic Area: Genetic Disease Product Name: Cevenfacta

              Highest Development Status: Approved Product Type: Large molecule

              Partner/Sponsor/Collaborator: Not Applicable

              Deal Size: Not Applicable Upfront Cash: Not Applicable

              Deal Type: Not Applicable July 25, 2022

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              LFB

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              CHMP Recommends Cevenfacta to Control Bleeding Episodes in Patients With Congenital Haemophilia

              Details:

              Positive opinions by CHMP were issued as a recommendation for marketing authorization was adopted for Cevenfacta (eptacog beta (activated)). Although FDA has approved SEVENFACT as first bypassing agent in over 20 years for patient with hemophilia A or B with inhibitor in 2020.

              Lead Product(s): Eptacog Beta

              Therapeutic Area: Genetic Disease Product Name: Cevenfacta

              Highest Development Status: Approved Product Type: Large molecule

              Partner/Sponsor/Collaborator: Not Applicable

              Deal Size: Not Applicable Upfront Cash: Not Applicable

              Deal Type: Not Applicable May 20, 2022

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              LFB

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              LFB Announces FDA Approval of SEVENFACT for the Treatment of Adults and Adolescents with Hemophilia A or B with Inhibitors

              Details:

              An exclusive license for the commercialization of the product in the USA and Canada has been granted to HEMA Biologics, a joint venture between LFB and US WorldMeds.

              Lead Product(s): Eptacog Alfa

              Therapeutic Area: Genetic Disease Product Name: Sevenfact

              Highest Development Status: Approved Product Type: Large molecule

              Partner/Sponsor/Collaborator: HEMA Biologics

              Deal Size: Not Applicable Upfront Cash: Not Applicable

              Deal Type: Not Applicable April 06, 2020

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              Minakem offers CDMO services for API & HPAPI, generics, regulatory expertise, track record performance & FDA & GMP certifications.
              ChemWerth works in generic API development & supply, non-infringement patent strategy development and regulatory support.
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