· On Dec. 8, the U.S. Food and Drug Administration (FDA) approved:
· Vonvendi, von Willebrand factor (Recombinant), for use in adults 18 years of age and older who have von Willebrand disease (VWD). Vonvendi is the first FDA-approved recombinant von Willebrand factor, and is approved for treatment and control of bleeding episodes in adults diagnosed with VWD. Read more.
· Kanuma (sebelipase alfa) as the first treatment for patients with lysosomal acid lipase (LAL) deficiency. Read more.
FDA approves new drugs
*Online Bonus Content: This has not been peer reviewed. The views and opinions expressed here are those of the author and do not necessarily reflect the opinions or recommendations of the American Nurses Association, the Editorial Advisory Board members, or the Publisher, Editors and staff of American Nurse Journal.
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