CRVO

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CervoMed's Neflamapimod Awarded UK Innovation Passport for DLB Treatments

CervoMed Inc. received an Innovation Passport for neflamapimod under the UK's ILAP program to accelerate its development for Lewy body dementia. Regulatory approval marks a significant step toward addressing this unmet medical need.

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CervoMed releases clinical data supporting neflamapimod for DLB

CervoMed released new analyses from its Phase 2b trial reinforcing neflamapimod's efficacy. The data supports selecting the 50 mg dose for Phase 3, enhancing investor confidence in the company's dementia pipeline.

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CervoMed closes $10M registered direct offering at $4.00 per share

CervoMed Inc. completed a registered direct offering of 2.5 million shares at $4.00 per share, raising $10 million gross proceeds for working capital and general corporate purposes. The funding supports the clinical-stage biotech's development of neflamapimod for age-related brai

View filing at SEC.gov →
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