TAUVID
Details
- Status
- Prescription
- First Approved
- 2020-05-28
- Routes
- INTRAVENOUS
- Dosage Forms
- SOLUTION
TAUVID Approval History
What TAUVID Treats
3 indicationsTAUVID is approved for 3 conditions since its original approval in 2020. These indications span multiple therapeutic areas including oncology, immunology, and more.
- Alzheimer's Disease
- Chronic Traumatic Encephalopathy
- Cognitive Impairment
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Active Pipeline
Ongoing clinical trials by development phase
Key Completed Trials
Completed studies with published results, ranked by significance
Trial Timeline
Full development history with FDA approval milestones
Understanding FDA Approval Types
| Count | Type | What it means |
|---|---|---|
| - | ORIG | Original approval - drug first enters market |
| - | SUPPL - Efficacy | New indication (new disease/condition approved) |
| - | SUPPL - Labeling | Label text changes (warnings, dosing updates) |
| - | SUPPL - Manufacturing | Production changes (new facility) |
| - | SUPPL - Chemistry | Formulation changes (new dosage strength) |
Green lines in the timeline show ORIG and Efficacy approvals - the clinically meaningful milestones.
TAUVID FDA Label Details
ProIndications & Usage
FDA Label (PDF)TAUVID is indicated for use with 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). TAUVID 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). Limitations of Use TAUVI...
TAUVID Patents & Exclusivity
Patents (16 active)
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Data Sources
Data sourced from official FDA and NIH databases. Click links to verify on original sources.