Early Phase 1
Completed N=36
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
| Outcome | Result | p-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
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.