On March 22,
the U.S. FDA approved pembrolizumab (Keytruda) in combination with chemotherapy
for a subset of patients with advanced
esophageal or gastroesophageal carcinoma. On March 27, the U.S. FDA
approved idecabtagene vicleucel (Abecma), a BCMA-targeted CAR T cell therapy,
for a subset of patients with multiple
myeloma. This is the first cell-based gene therapy approved by the FDA for
the treatment of multiple myeloma.
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Wednesday, April 7, 2021
U.S. FDA News
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