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[18F]AV-1451 for Alzheimer's Disease
Phase 2
Waitlist Available
Led By Denise Park, PhD
Research Sponsored by Neil M Rofsky, MD, MHA
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 1-year post study completion
Awards & highlights
Study Summary
This trial will use tau positron emission tomography (PET) scans to study tau deposition in adults of different ages and how it relates to cognition and amyloid deposition.
Eligible Conditions
- Alzheimer's Disease
- Cognitive Decline
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ 1-year post study completion
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~1-year post study completion
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
Standardized Uptake Value Ratios (SUVrs) Calculated From [18F]AV-1451 PET Scans
Secondary outcome measures
Relationship of Amyloid Accumulation to Tau Burden
Relationship of Tau Burden to Cortical Thickness
Relationship of Tau Burden to Episodic Memory Function
+8 moreSide effects data
From 2022 Phase 2 trial • 125 Patients • NCT040805447%
Elevated blood pressure
1%
Black dot in visual field
1%
Muscle soreness in injection arm
1%
Neck rash
1%
Diarrhea, drowsiness, nausea
100%
80%
60%
40%
20%
0%
Study treatment Arm
Follow up DLBS Participants
Trial Design
1Treatment groups
Experimental Treatment
Group I: Follow up DLBS participantsExperimental Treatment2 Interventions
Eight to ten year follow-up DLBS participants who were cognitively normal at the time of enrollment from 2008 to 2014.
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
[18F]AV-1451
2019
Completed Phase 2
~130
Positron Emission Tomography
2008
Completed Phase 2
~2240
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Who is running the clinical trial?
Neil M Rofsky, MD, MHALead Sponsor
1 Previous Clinical Trials
80 Total Patients Enrolled
Denise Park, PhDPrincipal InvestigatorUniversity of Texas at Dallas
1 Previous Clinical Trials
50 Total Patients Enrolled
Frequently Asked Questions
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