Research Impact

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Publications

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Trial Results

0

Published trial results

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0

Total citations

Drug Portfolio

Analytics

Trial Phases

Phase 11
Phase 22
Phase 310

Trial Status

Completed10
Terminated2

Role Distribution

Other Roles12

Activity Timeline

Clinical Trials (12)

NCT00168025Phase 3Completed
Efficacy and Safety of Intravenous Immunoglobulin IgPro10 in Patients With Primary Immunodeficiencies (PID)
AgammaglobulinemiaCommon Variable ImmunodeficiencyIgG Deficiency
Studydirector

Showing 10 of 12 trials

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Collaboration Network

1 collaborators·0 connections
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CO
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Publications (0)

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Clinical Trials (12)

Showing 12 of 12 trials

NCT03375606Phase 1StudyDirector

Assessing the Safety and Tolerability of CSL730 in Healthy Caucasian and Japanese Adults

Healthy
Terminated
NCT03221842Phase 3StudyDirector

Efficacy and Safety of Human Plasma-derived C1-esterase Inhibitor as add-on to Standard of Care for the Treatment of Refractory Antibody Mediated Rejection (AMR) in Adult Renal Transplant Recipients

Antibody-mediated Rejection
Terminated
NCT02427217StudyDirector

An Observational Cohort Study of the Safety and Efficacy of Fibrinogen Concentrate, Human (FCH) in Subjects With Congenital Fibrinogen Deficiency

Congenital Fibrinogen Deficiency
Completed
NCT02053792Phase 3StudyDirector

A Safety and Efficacy Extension Study of a Recombinant Fusion Protein Linking Coagulation Factor IX With Albumin (rIX-FP) in Patients With Hemophilia B

Hemophilia B
Completed
NCT00168025Phase 3StudyDirector

Efficacy and Safety of Intravenous Immunoglobulin IgPro10 in Patients With Primary Immunodeficiencies (PID)

AgammaglobulinemiaCommon Variable ImmunodeficiencyIgG Deficiency
Completed
NCT00292981Phase 3StudyDirector

C1 Esterase Inhibitor in Hereditary Angioedema (HAE)(Extension Study)

Hereditary Angioedema
Completed
NCT00719680Phase 3StudyDirector

Extension Study of Subcutaneous Immunoglobulin Human in Patients With Primary Immunodeficiency (PID)

Primary Immune Deficiency
Completed
NCT01486927Phase 2/3StudyDirector

An Open-label Safety, Efficacy and Pharmacokinetic Study of a Recombinant FVIII Compared to Recombinant Human Antihemophilic FVIII in Patients With Severe Hemophilia A

Hemophilia A
Completed
NCT01496274Phase 2/3StudyDirector

A Safety and Efficacy Study of a Recombinant Fusion Protein Linking Coagulation Factor IX With Albumin (rIX-FP) in Patients With Hemophilia B

Hemophilia B
Completed
NCT01662531Phase 3StudyDirector

A Safety, Efficacy and Pharmacokinetics Study of a Recombinant Fusion Protein Linking Coagulation Factor IX With Albumin (rIX-FP) in Children With Hemophilia B

Hemophilia B
Completed
NCT02093897Phase 3StudyDirector

Pharmacokinetic, Efficacy, and Safety Study of Recombinant Factor VIII Single Chain (rVIII-SingleChain) in Children With Severe Hemophilia A

Congenital Hemophilia A
Completed
NCT02172950Phase 3StudyDirector

An Open-label Safety and Efficacy Study of Recombinant FVIII in Patients With Severe Hemophilia A

Hemophilia ASevere Hemophilia A
Completed

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