Tauvid FDA Approval History
Tauvid (flortaucipir F 18) is a radioactive diagnostic agent indicated for positron emission tomography (PET) imaging of the brain to estimate the density and distribution of aggregated tau neurofibrillary tangles (NFTs) in adult patients with cognitive impairment who are being evaluated for Alzheimer’s disease (AD).
Development Timeline for Tauvid
|May 28, 2020||Approval FDA Approves Tauvid (flortaucipir F 18 injection) for Use in Patients Being Evaluated for Alzheimer's Disease|
|Sep 5, 2018||Lilly Announces Positive Phase 3 Results in Study of Flortaucipir PET Imaging Agent|
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