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Orphan Drug Application as von Willebrand patient 
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zohenten0k1w
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Dołączył: 16 Mar 2011
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PostWysłany: Pią 9:29, 29 Kwi 2011  

Thrombotargets Corp announced today that it has submitted its Orphan Drug Application of TT-103MH to the FDA for bleeding treatment in von Willebrand patients.[/b]
Thrombotargets Corporation announced today that it has submitted its Orphan Drug Application of its Human Recombinant protein known as TT-103MH to the United States Food and Drug Administration (FDA) for bleeding dispose in von Willebrand patients “ We are extremely pride and remain very optimistic that the FDA ambition look favorably ashore this nomination, said Dr. Pedre?o Thrombotargets President and CEO, “We remain very optimistic given the early Laboratory results,[link widoczny dla zalogowanych], that demonstrate that TT-103MH namely a viable and a very effective alternative to present replacement treatment in hereditary coagulation disorders for von Willebrand diseases and thinking previous TT-103MH Orphan Drug Designation for the treatment of Hemophiliacs ” said Dr. Pedre?o president and CEO.
The FDA grants orphan pill status for pill candidates that are proposed to treat infrequent life-threatening diseases that, at the time of applying, affect not more than 200,[link widoczny dla zalogowanych],000 patients in the United States. The drug must have the competence to invest meaningful patient benefit over currently accessible treatment or fill an unmet remedial need. Orphan drug designation entitles Thrombotargets corp. to 7 annuals of mart exclusivity in the United States above FDA agreement, provided that Thrombotargets Corp. continues to meet definite conditions built at the FDA.
About Thrombotargets Group
Thrombotargets[b] is a privately held team of Biotech companies focused in the breakthrough and development of innovative drugs in Haemostasis, Thrombosis and Atherosclerosis. The corporation has a digit of latent fashionable drugs in development internally and its proprietary targets and innovative uHTS platforms are used for internal drug finding procedures, as well as for out-licensing and partnering of new research projects.


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