| Condition | Additional Trial Information |
| Anticoagulant Reversal | Efficacy and Safety Study of BERIPLEX® P/N Compared With Plasma in Patients on Anticoagulant Therapy Who Require Emergency Surgery or Invasive Intervention
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| Acute Major Bleeding: Blood Coagulation Disorders | Efficacy and Safety Study of BERIPLEX® P/N Compared With Plasma in Patients With Acute Major Bleeding Caused by Anticoagulant Therapy
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| Chronic Inflammatory Demyelinating Polyneuropathy (CIDP) | Study of Efficacy and Safety of Privigen in Subjects with Chronic Inflammatory Demyelinating Polyneuropathy
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Congenital Fibrinogen Deficiency
| Fibrinogen Concentrate (Human) − Efficacy and Safety Study
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Emphysema Caused by API Deficiency
| Study of Zemaira i.v. Administration in Subjects Who Completed a 2-Year Controlled Study With This Treatment and Have Emphysema Due to alpha1 -Proteinase Inhibitor Deficiency.
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| Emphysema Caused by API Deficiency | Zemaira in Subjects With Emphysema Due to Alpha1-Proteinase Inhibitor (API) Deficiency
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| Factor XIII Deficiency | A Study of Factor XIII Concentrate in Subjects With Congenital Factor XIII Deficiency
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| Healthy | Safety, Tolerability and Pharmacokinetics of CSL112 in Healthy Volunteers
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| Hemophilia A | Study of a Plasma-Derived von Willebrand Factor/Factor VIII Concentrate (vWF/FVIII) , Biostate®, in Subjects with Hemophilia A
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| Hemophilia A | Study of Biostate® in Children with Hemophilia A
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| Hemophilia B | Safety and Pharmacokinetic Study of a Recombinant Coagulation Factor IX Albumin Fusion Protein in Subjects with Hemophilia B
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| Primary Immune Deficiency | Safety Study of Subcutaneous Ig NextGen 16% in Patients With Primary Immunodeficiency
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| Von Willebrand Disease | Study of a Plasma-Derived Von Willebrand Factor/Factor VIII Concentrate (vWF/FVIII), Biostate®, in Subjects With Von Willebrand Disease
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| Von Willebrand Disease | Study of Biostate® in Children with Von Willebrand Disease
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| Von Willebrand Disease | Extension Study of Biostate® in Subjects with Von Willebrand Disease
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