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NCT03391765 · ClinicalTrials.gov registry record · Phase 2

An Extension Study of ABBV-8E12 in Progressive Supranuclear Palsy (PSP)

A Phase 2 study, sponsored by AbbVie.

Terminated
Registry status
Phase 2
Development phase
142
Enrollment target

NCT03391765: Clinical Trial Phase 2 study, sponsored by AbbVie.

NCT03391765 is a Phase 2 study that was terminated before completion, run by AbbVie. The registered enrollment target is 142 participants, roughly in line with the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT03391765, a Phase 2 study, was terminated before completion, sponsored by AbbVie.

TERMINATED
Registry status
Phase 2
Development phase
142 participants
Enrollment target

Study Summary

The purpose of this study was to assess the long-term safety and efficacy of ABBV-8E12 (tilavonemab) in participants with progressive supranuclear palsy (PSP).

Primary Outcome

The PSPRS consists of 28 items grouped in six domains: daily activities (by history); behavior; bulbar; ocular motor; limb motor; and gait/midline. Items are scored on a 0 to 4 scale, except for six items that are scored on a 0 to 2 scale, with the total score ranging from 0 to 100. Higher scores indicate more severe disability or movement abnormality. Positive values indicate worsening from baseline.

Interventions

  • DRUG ABBV-8E12
  • DRUG Placebo solution for IV infusion on Day 15

Trial Details

FieldValue
Enrollment Target 142 participants
Start Date 2018-01-24
Est. Completion 2019-12-13
Phase Phase 2
AbbVie

526 total trials

Why NCT03391765 stopped before completion

NCT03391765 is an interventional study that assigns participants to a tested intervention. The registered 142 participants enrollment target is mid-sized for trials with a published cap, roughly in line with the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target.

The record links to 0 conditions, and to 2 interventions - of which ABBV-8E12 is the first listed.

NCT03391765 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT03391765 about?

NCT03391765 is a clinical study titled "An Extension Study of ABBV-8E12 in Progressive Supranuclear Palsy (PSP)". The purpose of this study was to assess the long-term safety and efficacy of ABBV-8E12 (tilavonemab) in participants with progressive supranuclear palsy (PSP).

What is the current status of trial NCT03391765?

This trial is currently terminated. It is a Phase 2 study. The enrollment target is 142 participants. The study started on 2018-01-24. Estimated completion is 2019-12-13.

What interventions are being tested in trial NCT03391765?

The interventions under investigation include: ABBV-8E12 (DRUG), Placebo solution for IV infusion on Day 15 (DRUG).

Who is sponsoring clinical trial NCT03391765?

This trial is sponsored by AbbVie, which has 526 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT03391765's enrollment target sits among peer trials

142 507th of 2000 higher than 1,491 of 2,000 other Phase 2 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 2 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

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Source: ClinicalTrials.gov NCT03391765, the US trial registry maintained by the National Library of Medicine. NCT03391765 (mid enrollment · none site footprint · terminated) retrieved and formatted by PlainTrial, see methodology.