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For adults with CIDP stabilized on IVIg
PROVEN CIDP CONTROL
Greater Freedom for Everyday Living
Hizentra is indicated for maintenance therapy in adults with chronic inflammatory demyelinating polyneuropathy (CIDP) to prevent relapse of neuromuscular disability and impairment.
-Limitation of Use: Maintenance therapy in CIDP has been systematically studied for 6 months and for a further 12 months in a follow-up study. Continued maintenance beyond these periods should be individualized based on patient response and need for continued therapy.
Discover the latest innovation in Ig
Hizentra is the first and only Ig available in prefilled syringes
Hizentra may help your CIDP patients address challenges with IVIg
Clinical challenges in CIDP:
- In some patients, poor venous access can make IV infusion difficult1
- Systemic adverse reactions, such as headache and fever, can occur2
Lifestyle burdens in CIDP:
- IV infusions can be costly and constraining3
- Travel to an infusion clinic can be time-consuming and require missing work3
*Based on equivalent dosing in grams. †Hizentra may be administered in 1 or 2 infusions over 1 or 2 consecutive days.
Hizentra is:
- A 20% immunoglobulin, half the volume of 10% IVIg*
- Infused in smaller doses more frequently than IVIg
- Subcutaneous, so no need to find a vein
Hizentra can be:
- Conveniently self-administered, allowing patients to infuse at an appropriate place and time
- Infused in a median time of ~1 hour per infusion†
- Adjusted to meet patient needs, with 2 safe and effective dosing options
Consider Hizentra for patients with CIDP who:
Experience IV-Related systemic adverse reactions
Have venous access issues
Clinical Challenges
Require more frequent IV infusions
Seek flexibiltiy, freedom, and control
Lifestyle Burdens
Photos do not depict actual patients
Watch Dr. Peter Van den Bergh, lead author, take you through the EAN/PNS guideline highlights
Learn about support services
Below are areas you may find especially helpful when providing Hizentra to your patients.
Voluntary withdrawal of specific Hizentra vial lots.