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The Danish national patient registry: a review of content, data quality, and research potential

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The US FDA approved it on January 6, 2023, through an accelerated approval pathway on the basis of evidence of amyloid removal in a phase 2 trial (NCT01767311) and because it had a likelihood of having clinical benefits [41] A double-blind, placebo-controlled phase 2 trial recruited 856 patients with AD with mild cognitive impairment (MCI) or mild dementia and verified amyloid pathology through amyloid PET or CSF A1-42 [42]

doi: 10.1016/j.jconrel.2025.113670 208 ShinYEChoiJWParkYIKimHK

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Quantification of myocardial blood flow with ultrasound-induced destruction of microbubbles administered as a constant venous infusion