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Regulatory acceleration via ILAP can lower development risk and improve visibility to partners/investors, often leading to a rerating of biotech names with later-stage potential.
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CRVO's CervoMed announced neflamapimod received the UK's Innovation Passport for ILAP in DLB, signaling accelerated regulatory support and closer NHS collaboration. This designation could shorten development timelines and boost partnering prospects ahead of a planned Phase 3 in DLB, potentially lifting CRVO's valuation even though DLB remains the primary driver.
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