Mode
Text Size
Log in / Sign up
Early Phase 1 Completed N=36 Diagnostic

Exploratory Evaluation of Flortaucipir Injection in Healthy Volunteers and Cognitively Impaired Subjects

Alzheimer Disease
Source: ClinicalTrials.gov NCT04474405 ↗
Enrolled (actual)
36
Serious AEs
0.0%
Results posted
Sep 2020
Primary outcomePrimary: Brain Flortaucipir Uptake — 1.780; 1.317; 1.128; 1.107 standardized uptake value ratio (SUVr)

Summary

This early phase 1 study explored the brain uptake, retention, and safety of flortaucipir and obtained preliminary information regarding dosimetry of flortaucipir.

Outcome Measures

OutcomeResultp-value
PRIMARY
Brain Flortaucipir Uptake
1.780; 1.317; 1.128; 1.107
PRIMARY
Flortaucipir Whole Body Effective Dose
0.0241
SECONDARY
Flortaucipir PET Correlations With Cognitive Assessments (Mini-mental State Exam)
-0.404
SECONDARY
Flortaucipir PET Correlations With Cognitive Assessments Cognitive Assessments (Digit Symbol Substitution Test)
-0.273
SECONDARY
Flortaucipir PET Correlations With Cognitive Assessments Cognitive Assessments (Alzheimer's Disease Assessment Scale)
0.220

Eligibility Criteria

Inclusion Criteria

  • Healthy volunteers had an Mini-Mental State Examination (MMSE) score of ≥ 29;
  • MCI due to Alzheimer's disease (AD) consistent with National Institute on Aging (NIA)-Alzheimer's Association working group's on diagnostic guidelines for AD (Alzheimer's Dementia 7:270-9, 2011)
  • Possible or probable AD: Met clinical criteria for possible or probable AD based on the NIA-Alzheimer's Association working group's on diagnostic guidelines for AD (Alzheimer's Dementia 7:263-9, 2011)

Exclusion Criteria

  • Current clinically significant psychiatric disease.
  • Evidence of structural abnormalities such as major stroke or mass on MRI that would have made a diagnosis of impairment due to AD unlikely or was likely to interfere with interpretation of a PET scan on MRI.
  • Claustrophobic or otherwise unable to tolerate the imaging procedure.
  • Current clinically significant cardiovascular disease or clinically significant abnormalities on screening electrocardiogram (including, but not limited to, corrected QT interval >450 msec).
  • Current clinically significant infectious disease, endocrine or metabolic disease, pulmonary, renal or hepatic impairment, or cancer
  • History of alcohol abuse or substance abuse or dependence
  • Female subjects of childbearing potential who were not surgically sterile, not refraining from sexual activity or not using reliable methods of contraception.
  • Required medications with a narrow therapeutic window
  • Received a non-study related radiopharmaceutical imaging or treatment procedure within 7 days prior to imaging session
  • Receiving any investigational medications or had participated in a trial with investigational medications within the last 30 days
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT04474405). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication. Informational only — not medical advice.

Back to search