ImmunityBio's FDA decision on Anktiva
What the company said
“License Application (sBLA) for ANKTIVA plus BCG in patients with BCG-unresponsive NMIBC with papillary disease without CIS and assigned a PDUFA target action date of January 6, 2027”
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Breakaway, ImmunityBio's FDA decision on Anktiva, Nov 2, 2026, getbreakaway.com/biotech/IBRX-anktiva
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