CSL Behring is committed to providing the support and resources you need to help you start and stay on your Ig therapy, with services designed to make treatment more accessible and manageable.
The Copay Support Program helps eligible Privigen patients with commercial insurance by assisting with out-of-pocket expenses for Privigen, up to $20,000 in copay assistance per calendar year.
Most people with commercial insurance pay $0 out-of-pocket*
* Subject to terms and conditions of the copay assistance program. To read the full terms and conditions, visit CSL Copay Terms and Conditions. CSL Behring reserves the right to rescind, revoke, or amend the program at any time without notice.
This program allows eligible patients to continue receiving Privigen even if you have a lapse in your insurance coverage†
† Enrollment required. Subject to terms and conditions. For the Assurance program, visit cslbehringassurance.com.
Helps provide therapy to qualified people who are uninsured or underinsured
Make the most of your Privigen therapy
Get information to help you talk to your doctor about Privigen, an IVIg therapy for CIDP.
Download the CIDP Patient Education Brochure
Make the most of your Privigen therapy
Get information to help you talk to your doctor about Privigen, an IVIg therapy for PI.
Download the PI Patient Education BrochureGlobal nonprofit organization that provides education, research, and advocacy related to Guillain-Barré syndrome, CIDP, and related conditions.
Supports research and awareness of autoimmune diseases to advance diagnosis and effective treatment.
Information resource for patients with peripheral neuropathy and their families and healthcare providers. Fosters research into peripheral neuropathy therapies through collaboration with neuroscientists and physicians.
Healthcare professionals, researchers, advocates, patients, and their families working together to improve the diagnosis, treatment, and quality of life of people affected by primary immunodeficiency.
Global resource for up-to-date information and support related to primary immunodeficiency disorders. Devoted to early diagnosis and effective treatment of PI through research, education, advocacy, awareness, and screening.
Serves patients, practitioners, caregivers, advocates, and key disease stakeholders through education, advocacy, research, and support.
Supports innovative research, specialty medical training, and comprehensive patient care for childhood cancer and blood disease therapies at New York Presbyterian-Weill Cornell Medical Center.
If you are living with CIDP, PI, or Chronic ITP, you may want additional support and information. Check out the links below for general information.
National Organization for Rare Disorders (NORD)NORD is a nonprofit patient advocacy organization that is committed to the identification, treatment, and cure of rare diseases and disorders. Along with more than 300 patient-organization members, NORD provides educational programs, advocacy, research, and patient services.
National Family Caregivers AssociationAlso known as the Caregivers Action Network (CAN) is a national non-profit organization that provides education, peer support, and resources to family caregivers across the country free of charge.
National Institutes of HealthA part of the U.S. Department of Health and Human Services, NIH is the largest biomedical research agency in the world. NIH investigates the nature and behavior of living systems and applies the findings to enhance health, lengthen life, and reduce illness and disability.
National Library of Medicine (NLM)The National Library of Medicine (NLM) is part of the National Institutes of Health, providing print and electronic information on a wide range of topics. The NLM is a reliable source of health information about diseases, conditions, and wellness issues, and serves as a clearinghouse for clinical trials.