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Tauvid Approval History

FDA Approved: Yes (First approved May 28, 2020)
Brand name: Tauvid
Generic name: flortaucipir F 18
Dosage form: Injection
Company: Eli Lilly and Company
Treatment for: Diagnosis and Investigation

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 History and FDA Approval Process for Tauvid

DateArticle
May 28, 2020Approval FDA Approves Tauvid (flortaucipir F 18 injection) for Use in Patients Being Evaluated for Alzheimer's Disease
Sep  5, 2018Lilly Announces Positive Phase 3 Results in Study of Flortaucipir PET Imaging Agent

Further information

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