beeldscherm schreef op 25 januari 2018 11:21:
[beeldscherm schreef op 25 jan 2018 om 10:20:
Hemophilia Treatment Drugs Market to Raise at a CAGR of 5.4% During 2016 - 2024
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The various products available in the global hemophilia treatment drugs market are recombinant coagulation factor concentrates, plasma derived coagulation factor concentrates, desmopressin, and antifibrinolytic agents. Of these, the recombinant coagulation factor concentrates are poised to lead the global market as the segment estimated to acquire a share of 46.9% by the end of 2024. The growing preference for recombinant factor therapies due to the low risk of blood-related infections is expected to fuel the growth of this segment.
www.digitaljournal.com/pr/3634115...]Pharming Acquires New Product Leads Through The Acquisition Of Certain Assets Of TRM SASU For € 0.5 Million In Cash
Leiden, The Netherlands, 19 August 2014. Biotech company Pharming Group NV (“Pharming” or “the Company”) (Euronext: PHARM) today announced that through the acquisition of certain assets of Transgenic Rabbit Models SASU (TRM), a private French company in liquidation; for € 0.5 million in cash, it has gained access to five potential new product leads (founder rabbits); recombinant- human (rh)-a-glucosidase for the treatment of Pompe’s disease, rh-a-galactosidase for the treatment of Fabry’s disease, rh-ß-cerebrosidase for the treatment of Gaucher’s disease, rh- Factor VIII for the treatment of Haemophilia-A and rh- Factor IX for the treatment of Haemophilia-B.
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Bruno Giannetti, Pharming’s Chief Operating Officer commented, “Through this acquisition, we have added two important assets; the capability to create rabbit founders as an addition to our FDA and EMA validated technology platform, and, at the same time, a number of product leads. The latter means that we will not only be able to strengthen our Factor VIII project with SIPI by adding an additional source of founder rabbits, but also to accelerate, by possibly as much as two years, our ability to develop additional products in therapeutic areas where our technology platform is particularly efficient -the development of treatments for rare genetic and life-threatening diseases such as Pompe’s, Fabry’s and Gaucher’s disease-. It is these kinds of diseases that require the complex proteins that continue to pose serious technical and cost challenges to cell based production methods
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