European Commission grants conditional marketing authorization for ImmunityBio ANKTIVA with BCG in NMIBC CIS

Reuters

Feb 18

European Commission grants conditional marketing authorization for ImmunityBio ANKTIVA with BCG in NMIBC CIS

ImmunityBio Inc. said the European Commission granted conditional marketing authorization for ANKTIVA (nogapendekin alfa inbakicept) in combination with BCG to treat adult patients with BCG-unresponsive non-muscle invasive bladder cancer carcinoma in situ, with or without papillary tumors. The authorization covers all 27 EU member states plus Iceland, Norway and Liechtenstein, expanding the product’s authorized footprint to 33 countries across the U.S., U.K., Saudi Arabia and the EU.

Disclaimer: This news brief was created by Public Technologies (PUBT) using generative artificial intelligence. While PUBT strives to provide accurate and timely information, this AI-generated content is for informational purposes only and should not be interpreted as financial, investment, or legal advice. Immunitybio Inc. published the original content used to generate this news brief on February 18, 2026, and is solely responsible for the information contained therein.

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