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[18F]Florbetapir for Alzheimer's Disease

Phase 1
Waitlist Available
Led By David Russell
Research Sponsored by Invicro
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
Be older than 65 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 1 year
Awards & highlights

Study Summary

The overall goal of this protocol is to compare amyloid burden assessed by amyloid PET to plasma P-tau217 levels.

Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~1 year
This trial's timeline: 3 weeks for screening, Varies for treatment, and 1 year for reporting.

Treatment Details

Study Objectives

Outcome measures can provide a clearer picture of what you can expect from a treatment.
Primary outcome measures
Creation of a database of brain amyloid deposition by region using PET signal-to-noise ratio, SUVr .
Secondary outcome measures
Creation of a database of blood P-tau217 and other blood biomarkers.

Trial Design

1Treatment groups
Experimental Treatment
Group I: [18F]FlorbetapirExperimental Treatment1 Intervention
Participants will undergo amyloid PET imaging with an approved amyloid radiotracer (ie, [18F]Florbetapir (Amyvid™)) to assess β-amyloid neuritic plaque density.

Find a Location

Logistics

Participation is compensated

You will be compensated for participating in this trial.

Who is running the clinical trial?

InvicroLead Sponsor
16 Previous Clinical Trials
185 Total Patients Enrolled
David RussellPrincipal InvestigatorInvicro

Frequently Asked Questions

These questions and answers are submitted by anonymous patients, and have not been verified by our internal team.
Recent research and studies
clinicaltrials.govStudy
Plasma P-tau2017 and Quantitative Amyloid PET Imaging
2021. "Plasma P-tau2017 and Quantitative Amyloid PET Imaging". ClinicalTrials.gov. https://clinicaltrials.gov/ct2/show/NCT05164536.
~56 spots leftby Apr 2025
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