Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

NCT02167594 · ClinicalTrials.gov registry record · Phase 1

Tau Imaging in Subjects With Progressive Supranuclear Palsy, Corticobasal Degeneration and Healthy Volunteers

A Phase 1 study, sponsored by Avid Radiopharmaceuticals.

Completed
Registry status
Phase 1
Development phase
29
Enrollment target

NCT02167594: Completed Phase 1 study, sponsored by Avid Radiopharmaceuticals.

NCT02167594 is a Phase 1 study that has completed, run by Avid Radiopharmaceuticals. The registered enrollment target is 29 participants, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (52% lower). According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT02167594, a Phase 1 study, has completed, sponsored by Avid Radiopharmaceuticals.

COMPLETED
Registry status
Phase 1
Development phase
29 participants
Enrollment target

Study Summary

This study will evaluate flortaucipir for brain imaging of tau in subjects with progressive supranuclear palsy (PSP), corticobasal degeneration (CBD) and healthy volunteers.

Primary Outcome

A PSP/CBD (PSP = progressive supranuclear palsy; CBD = corticobasal degeneration) targeted composite Standardized Uptake Value ratio (SUVr) was calculated as the voxel-weighted average from the regional SUVr values of the left, right, and total globus pallidus and the dentate nuclei of the cerebellum for both the baseline and 9 month PET scans. Additionally, a global cortical Alzheimer's Disease (AD)-targeted cortical SUVr was calculated. For SUVr, a value of 1 signifies no flortaucipir activity

Interventions

  • DRUG Flortaucipir F18
  • PROCEDURE Brain PET scan

Trial Details

FieldValue
Enrollment Target 29 participants
Start Date 2014-08-12
Est. Completion 2016-07-11
Phase Phase 1
Avid Radiopharmaceuticals

42 total trials

What the finished NCT02167594 record still lists

NCT02167594 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 29 participants, a relatively small participant target, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (52% lower).

The record links to 0 conditions, and to 2 interventions - of which Flortaucipir F18 is the first listed.

NCT02167594 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT02167594 about?

NCT02167594 is a clinical study titled "Tau Imaging in Subjects With Progressive Supranuclear Palsy, Corticobasal Degeneration and Healthy Volunteers". This study will evaluate flortaucipir for brain imaging of tau in subjects with progressive supranuclear palsy (PSP), corticobasal degeneration (CBD) and healthy volunteers.

What is the current status of trial NCT02167594?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 29 participants. The study started on 2014-08-12. Estimated completion is 2016-07-11.

What interventions are being tested in trial NCT02167594?

The interventions under investigation include: Flortaucipir F18 (DRUG), Brain PET scan (PROCEDURE).

Who is sponsoring clinical trial NCT02167594?

This trial is sponsored by Avid Radiopharmaceuticals, which has 42 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT02167594's enrollment target sits among peer trials

29 1440th of 2000 higher than 554 of 2,000 other Phase 1 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 1 trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

Nationwide trials with similar profiles

Cross-condition peers matched on enrollment target and registry start date, not the same-condition list above.

Similar enrollment target

  • NCT02429557 · 29 participants · Phase 1

    Hemodynamic Mechanisms of Abdominal Compression in the Treatment of Orthostatic Hypotension in Autonomic Failure

  • NCT02568878 · 29 participants · Phase 3

    Creatine for Depressed Male and Female Methamphetamine Users

  • NCT03014401 · 29 participants · NA

    The Effect of Adipose-Derived Stem Cells for Knee Osteoarthritis

  • NCT03128996 · 29 participants · Phase 1

    Reduced Intensity Conditioning and Familial HLA-Mismatched BMT for Non-Malignant Disorders

Similar registry start date

  • NCT05962346 · started 2026-12 · NA

    Fetal Endoscopic Tracheal Occlusion for Congenital Diaphragmatic Hernia

  • NCT07125183 · started 2026-12 · Phase 2

    Study on Efficacy and Tolerability of Weekly Doxorubicin in Elderly Patients With Advanced or Metastatic Leiomyosarcoma

  • NCT07292298 · started 2026-11 · Phase 2

    Phase 2 Single-Arm Rectal Cancer Brachytherapy for Patients With Low-Lying Residual Adenocarcinoma After Total Neoadjuvant Therapy to Improve Organ Preservation Rates

  • NCT04263285 · started 2026-10 · NA

    Treatment of Depression Post-SCI

Source: ClinicalTrials.gov NCT02167594, the US trial registry maintained by the National Library of Medicine. NCT02167594 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.