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New PET tracers aim to spot tau tangles in rare brain disease

NCT ID NCT07348276

First seen Jan 17, 2026 · Last updated Jun 22, 2026 · Updated 18 times

Summary

This early-phase study tests two new imaging drugs, [18F]ABBV-964i and [18F]ABBV-965i, designed to light up tau protein buildup in the brain during a PET scan. Tau buildup is linked to Progressive Supranuclear Palsy (PSP), a rare movement and thinking disorder. The trial includes up to 24 adults (healthy volunteers and people with PSP) to check safety, radiation exposure, and how well the drugs show tau in the brain. Better imaging could help diagnose PSP earlier and track disease progression.

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This is a summary of the original study . Summaries may miss details or leave out important information. Before applying or accepting participation, make sure you have read and understood the full study. Curemydisease.com takes no responsibility whatsoever for anything missed, misunderstood, or acted upon as a result of our summary — we know it does not capture everything.

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Contacts and locations

Study contacts

  • Contact

    Phone: •••-•••-•••• Email: •••••@•••••

Locations

  • Invicro (dba Perceptive)

    RECRUITING

    New Haven, Connecticut, 06510, United States

    Contact Phone: •••-•••-••••

What this could mean

Our plain-language read of the trial. This is informational only — not medical advice or a prediction.

Active substance

[18F]ABBV-964i and [18F]ABBV-965i (imaging drugs used in PET scans)

What this could lead to

If successful, these imaging drugs could help doctors see tau buildup in the brain, leading to earlier and more accurate diagnosis of PSP and better tools for tracking the disease.

What could go wrong

This is a very early, small study (24 people) focused on safety and imaging quality, not treatment. The drugs may not work as hoped, and results may not apply to larger groups.

Conditions

The condition(s) this trial relates to.

Pick disease progressive supranuclear palsy tauopathy

As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.