We are part of the CSL Limited group of companies. See how we're Driven by Our Promise.
We collaborate with rare disease organizations to promote quality medical care and services.
We offer a variety of support programs and activities for the patients we serve.
We also aim to make sure that nothing holds you back from getting the therapies you need.
Our product portfolio focuses on innovation in new products, improved products and manufacturing expertise.
A clinical trial is a research study that is done to find out if medical treatments can improve people’s health.
We work every day as if someone’s life depends on it, because it does.
We manufacture products to treat a number of rare diseases.
Help us deliver on our promise to save lives and protect the health of people.
Diversity and inclusion are top priorities for CSL Behring.
Writing the Book on Sickle Cell Disease
Dr. Greg Kato, a CSL Behring medical expert, is among three editors of a new, deeply researched text on sickle cell disease. …
What Is It Like to Have Sickle Cell Disease?
In their own words, patients and caregivers describe the disease’s emotional toll.
Marking Sickle Cell Disease Awareness Month
U.S. recognizes important need for research into inherited blood condition.
Family Unites Against Sickle Cell Disease
Instead of the usual reunion, 50+ family members rolled up their sleeves to help those who have sickle cell disease.
An All-Too Common Rare Disease
Sickle cell disease patients have been waiting a long time for a breakthrough; CSL Behring’s expert on what’s next for those …
Sickle Cell Disease Caregivers' Guide
Caregivers play a multifaceted role. Here’s how to support a loved one who has this inherited blood disorder.
Santonio Holmes Tackles Sickle Cell Disease
The Steeler legend - and Dad to a son with the disease - visits our podcast to talk about his foundation that helps families …
COVID-19 and Sickle Cell Disease
Experts, including CSL Behring’s Dr. Greg Kato, weigh whether sickle cell patients are more at risk of severe impacts from co…
Sickle Cell Camp in Jamaica
“Hope Lives Here” connects Jamaican teens living with blood disorder.
Patients as Partners
Healthcare panel will explore how tech can build a bridge and involve patients every step of the way.
Don't Go It Alone
Mentors can help guide young sickle cell disease patients.
Advice for Young Sickle Cell Patients
Learn how young adult sickle cell disease patients can move out of pediatric care and take control of their health.
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