| Condition | Link to Additional Trial Information |
Acute Bleeding During Aortic Replacement Surgery
|
Haemocomplettan® P During Aortic Replacement |
| 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 |
| Acute Myeloid Leukemia |
Safety, Tolerability and Pharmacokinetics of CSL360 in the Treatment of Acute Myeloid Leukemia |
Blood Coagulation Disorders; Acute Major Bleeding |
Efficacy and Safety Study of BERIPLEX® P/N Compared With Plasma in Patients With Acute Major Bleeding Caused by Anticoagulant Therapy |
Congenital Fibrinogen Deficiency
|
Fibrinogen Concentrate (Human) − Efficacy and Safety Study  |
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. |
| Emphysema Caused by API Deficiency |
Zemaira in Subjects With Emphysema Due to Alpha1-Proteinase Inhibitor (API) Deficiency
|
Factor XIII Deficiency
|
A Study of the Use of Factor XIII Concentrate in Patients with Inherited FXIII Deficiency |
| Factor XIII Deficiency |
A Study of Factor XIII Concentrate in Subjects With Congenital Factor XIII Deficiency |
| Healthy Volunteers - Adults aged 65 years or younger |
A Study of the Efficacy, Safety and Tolerability of CSL Limited's Influenza Virus Vaccine Administered Intramuscularly in Healthy Adults |
| Healthy Volunteers - Adults aged 65 years or younger |
A Study to Determine the Immunogenicity and Safety of CSL Limited's Influenza Virus Vaccine Compared to a US Licensed Comparator Influenza Virus Vaccine |
Healthy Volunteers - Paediatric
|
Safety Study of CSL Limited's Influenza Virus Vaccine in the Paediatric Population Aged Between >= 6 Months to < 18 Years |
| Healthy Volunteers - Paediatric |
A Study to Determine the Immunogenicity and Safety of CSL Limited's Influenza Virus Vaccine Compared to a US Licensed Comparator Influenza Virus Vaccine in a Pediatric Population |
| Healthy Volunteers - Paediatric |
A Clinical Trial of CSL's 2009 H1N1 Influenza Vaccine (CSL425) in Healthy Children |
| Healthy Volunteers - Paediatric |
A Clinical Trial of CSL's 2009 H1N1 Influenza Vaccine (CSL425) in a Healthy Pediatric Population in the USA |
| Healthy Volunteers - Adults aged 18 years and older |
A Clinical Trial of CSL's 2009 H1N1 Influenza Vaccine (CSL425) in Healthy Adults |
| Healthy Volunteers - Adults aged 18 years and older |
A Clinical Trial of CSL's 2009 H1N1 Influenza Vaccine (CSL425) in Healthy Adults in the USA |
Hemophilia A
|
Study of a Plasma-Derived von Willebrand Factor/Factor VIII Concentrate (vWF/FVIII) , Biostate®, in Subjects with Hemophilia A  |
| Hereditary Angioedema |
C1 Esterase Inhibitor in HAE (Extension Study) |
| Primary Immune Deficiency |
Study of Subcutaneous Immune Globulin in Patients Requiring IgG Replacement Therapy |
| Primary Immune Deficiency |
Extension Study of Subcutaneous Immunoglobulin Human in Patients With Primary Immunodeficiency (PID) Requiring IgG Replacement Therapy (North America) |
| Primary Immune Deficiency |
Extension study of Subcutaneous Immune Globulin in Patients Requiring IgG Replacement Therapy (Europe) |
| Primary Immune Deficiency |
Subcutaneous Ig NextGen 16% in PID Patients |
| Primary Immune Deficiency |
Safety Study of Subcutaneous Ig NextGen 16% in Patients With Primary Immunodeficiency |
| Von Willebrand Disease |
Study of a Plasma-Derived Von Willebrand Factor/Factor VIII Concentrate (vWF/FVIII), Biostate®, in Subjects With Von Willebrand Disease |