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Innovation is in our DNA and is the core of everything we do at CSL Behring. Our team of over 1,700 R&D experts are dedicated to developing and delivering new therapies to solve unmet medical needs and save lives. We have created one of the largest and most efficient plasma collection networks in the world and strive to be the best at delivering safe and effective medicines for our patients.
was invested in R&D in 2017/18
in R&D investments in the last 5 years
research & development employees
Investment in R&D is an important driver for CSL Behring’s future growth. We have a high quality and potentially valuable portfolio of projects in various stages of development. We continue to make a balanced investment in the life cycle management and market development of existing products that bring short to mid-term commercial benefits, and we make strategic investments in longer term, higher risk and high opportunity new product development activities.
| Therapeutic Area | Condition | Description | |
| Bleeding Disorders |
Hemophilia A | An Open-label Safety and Efficacy Study of Recombinant FVIII in Patients With Severe Hemophilia A. | Learn More |
| Hemophilia B | A Safety and Efficacy Extension Study of a Recombinant Fusion Protein Linking Coagulation Factor IX With Albumin (rIX-FP) in Patients With Hemophilia B | Learn More | |
| Hemophilia A & B | A Study to Investigate the Pharmacokinetics, Efficacy, and Safety of rVIIa-FP (CSL 689) in Subjects With Hemophilia (A or B) and Inhibitors | Learn More | |
| Congenital Fibrinogen Deficiency | An Observational Cohort Study of the Safety and Efficacy of Fibrinogen Concentrate, Human (FCH) in Subjects With Congenital Fibrinogen Deficiency | Completed | |
| Von Willebrand | Study of Voncento® in Subjects With Von Willebrand Disease | Completed | |
| Warfarin Reversal | An Observational Study of the Risk of Thromboembolic Events Among Adult Patients Treated With KCENTRA® Compared With Plasma for Urgent Reversal of Vitamin K Antagonist Therapy in the Setting of Acute Major Bleeding | Learn More | |
| Cardiovascular | Acute Coronary Syndrome | Study to investigate CSL112 in Subjects With Acute Coronary Syndrome | Learn More |
| Coronary Heart Disease | Assessing the pharmacokinetics, safety, and tolerability of CSL112 in healthy Japanese and Caucasian adults | Learn More | |
| Immunoglobulins | Chronic Inflammatory Demyelinating Polyneuropathy | Extension Study of Maintenance Treatment with Subcutaneous Immunoglobulin (IgPro20) for Chronic Inflammatory Demyelinating Polyneuropathy (CIDP) | Learn More |
| Hereditary Angioedema (HAE) | A Multicenter, Randomized, Placebo-controlled, Parallel-arm Study to Investigate the Efficacy, Pharmacokinetics, and Safety of CSL312 in Subjects With Hereditary Angioedema | Learn More | |
|---|---|---|---|
| Pediatric CIDP | Randomized Study of Single vs. Multiple Privigen Dose Regimens in Pediatric CIDP | Learn More | |
| Primary Immune Deficiency (PID) | Safety and Tolerability of Higher Infusion Parameters of IgPro20 (Hizentra) in Subjects With Primary Immunodeficiency (PID) | Learn More | |
| Primary Immune Deficiency (PID) | Study of Immune Deficiency Patients Treated With Subcutaneous Immunoglobulin (IgPro20, Hizentra®) on Weekly and Biweekly Schedules | Completed | |
| Primary Immune Deficiency (PID) | Comparison of 2 Infusion Devices With Respect to Pharmacokinetics, Safety, and Tolerability of Hizentra: An Investigational Wearable Infusor and the Crono S-PID-50 Infusion Pump | Learn More | |
| Therapeutic Proteins | Other Inflammatory or immune system disorders | Dose escalation, placebo-controlled phase 1 study to assess the safety and tolerability of CSL324 in healthy adults | Learn More |
| Transplant | Antibody-mediated kidney transplant rejection | 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 in Adult Renal Transplant Recipients | Learn More |
CSL is a global specialty biotech with a strong commitment to funding research and development of medicines to support its continued growth. We operate as one integrated global research and development organization that assembles coordinated global project teams, drawing together staff from different countries depending on their expertise. Our teams rely on a project management framework that facilitates collaboration across national and cultural boundaries.
PARKVILLE, VIC
CSL Limited
Global Corporate HQ
R&D and Manufacturing
BROADMEADOWS, VIC
CSL Behring
R&D and Manufacturing
NORTH MELBOURNE, VIC
Bio21 Global Research and Translational Medicine Hub
MARBURG
CSL Behring
R&D and Manufacturing
KING OF PRUSSIA, PA
CSL Behring
Head Office and R&D
KANKAKEE, IL
CSL Behring
R&D and Manufacturing
PASADENA, CA
Calimmune
R&D
BERN
CSL Behring
R&D and Manufacturing
TOKYO
CSL Behring
R&D
WUHAN
Ruide
R&D and Manufacturing
