Sesen Bio, Inc. hopes to meet with US regulators as soon as possible to try and reinflate approval prospects for its lead investigational therapy, Vicineum, after the biotech received a complete response letter from the US Food and Drug Administration for the therapy’s use in BCG-unresponsive non-muscle invasive bladder cancer. The surprize setback seems to have dashed the drug’s chances of gaining first-mover status in the NMIBC market and address the high unmet medical need there.
Sesen surprized investors on 13 August by announcing receipt of the CRL following a priority review, just ahead of its...



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