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FDA biologics license application

Pharma & Biotech

ImmunityBio resubmits FDA application for ANKTIVA in bladder cancer after agency requests updated efficacy data

ImmunityBio has resubmitted its supplemental biologics license application to the U.S. Food and Drug Administration for ANKTIVA (nogapendekin alfa inbakicept) in combination with Bacillus Calmette-Guerin for BCG-unresponsive non-muscle invasive bladder cancer with papillary tumors, after the agency requested updated long-term efficacy data in March 2026. The resubmission follows a regulatory exchange that began in January

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Pharma & Biotech

Why Pierre Fabre Pharmaceuticals’ regulatory strategy for tabelecleucel matters for rare oncology approvals

Pierre Fabre Pharmaceuticals seeks an FDA path forward for tabelecleucel in EBV-positive PTLD after a Complete Response Letter. Discover what regulators may scrutinize next.

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