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Not yet recruiting Phase 2 Interventional

Flutemetamol F 18 Injection Formulation Comparison

ClinicalTrials.gov ID: NCT07873463

Public ClinicalTrials.gov record NCT07873463. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 15, 2026, 11:14 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Multicenter, Phase 2, Open-Label, Randomized, Crossover Comparison of Two Formulations of Flutemetamol F 18 Injection

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

VIZAMYL (flutemetamol F 18 injection) is a drug used during Positron Emission Tomography (PET) brain scans. It helps doctors detect the presence of amyloid protein, which is associated with Alzheimer's disease and other conditions affecting memory or thinking. A new formulation of this drug, called GE-287, has been developed. This new formulation may offer advantages for patient tolerability and can be produced more reliably and efficiently. The aim of the study is to determine whether the new formulation works as well as the current one in identifying amyloid in the brain, how it distributes in the body, and whether it is safe for use. The study will measure how much of the study drug goes to different organs (including the brain, heart, liver, and kidneys) and monitor for any side effects.

Study identification

NCT ID
NCT07873463
Recruitment status
Not yet recruiting
Study type
Interventional
Phase
Phase 2
Lead sponsor
GE Healthcare
Industry
Enrollment
20 participants

Conditions and interventions

Interventions

Drug

Eligibility (public fields only)

Age range
50 Years to 110 Years
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Sep 22, 2026 (Estimated)
Primary completion
Feb 25, 2027 (Estimated)
Completion
Feb 25, 2027 (Estimated)
Last update posted
Oct 14, 2026

2026 – 2027

United States locations

U.S. sites
6
U.S. states
2
U.S. cities
5
Facility City State ZIP Site status
Visionary Investigator Network Aventura Florida 33180 —
Meritt Island Research, LLC dba. Flourish Research Merritt Island Florida 32952 —
Visionary Investigator Network Miami Florida 33133 —
Visionary Investigator Network Miami Florida 33176 —
Clinical Site Partners, LLC dba Flourish Research Winter Park Florida 32789 —
Center for Advanced Research & Education LLC dba Flourish Research Gainesville Gainesville Georgia 30501 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT07873463, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Oct 14, 2026 · Synced Oct 15, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT07873463 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →