The FDA on December 20, 2018 approved ASPARLAS®, an asparagine specific enzyme, as a component of a multi-agent chemotherapeutic regimen for Acute Lymphoblastic Leukemia (ALL) in pediatric and young adult patients age 1 month to 21 years. This new product provides for a longer interval between doses compared to other available pegaspargase products. ASPARLAS® is a product of Servier Pharmaceuticals LLC.
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