KYMRIAH® (Tisagenlecleucel)

The FDA on August 30, 2017 granted regular approval to KYMRIAH®, for the treatment of patients up to age 25 years with B-cell precursor Acute Lymphoblastic Leukemia (ALL), that is refractory or in second or later relapse. KYMRIAH® is a product of Novartis Pharmaceuticals Corp.