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Inherited Orphan Blood Disorders Therapeutics Market to 2019 - Breakthrough Drugs Remain Elusive Against Backdrop of High Unmet Need
Date:1/29/2013

ma, Pipeline, Overview 65

Figure 51: Hereditary Angioedema, Pipeline, Pre-Clinical Molecule Comparison 66

Figure 52: Hereditary Angioedema Pipeline, Phase II Molecule Comparison 67

Figure 53: Hereditary Angioedema, Pipeline, Phase III Molecule Comparison 68

Figure 54: Hereditary Angioedema, Pipeline by Therapeutic Class 69

Figure 55: Hereditary Angioedema, Pipeline by Molecule Type 69

Figure 56: Hereditary Angioedema, Pipeline by Mechanism of Action 70

Figure 57: Inherited Orphan Blood Diseases Market, Deal Segmentation by Year, 2000–2012 72

Figure 58: Inherited Orphan Blood Diseases Market, Deal Segmentation by Indication 72

Figure 59: Inherited Orphan Blood Diseases Market, Deal Segmentation by Geography 73

Figure 60: Inherited Orphan Blood Diseases Market, Deal Segmentation by Value 73

Figure 61: Inherited Orphan Blood Diseases Market, Deal Segmentation by Deal Type 74

Figure 62: GBI Research Market Forecasting Model 80

 

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Pathology Industry: Inherited Orphan Blood Disorders Therapeutics Market to 2019 - Breakthrough Drugs Remain Elusive Against Backdrop of High Unmet Need

Nicolas Bombourg
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7. Grifols Initiates Safety Study of Inhaled Alpha1-Proteinase Inhibitor (Human) Following Orphan Drug Designation for Cystic Fibrosis
8. European Commission Grants Orphan Medicinal Product Designation for Emmaus Medicals Sickle Cell Treatment
9. CSL Behring Receives FDA Orphan Drug Designation for rIX-FP, a Novel Therapy in Development to Treat Congenital Factor IX Deficiency (Hemophilia B)
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