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NCT00651729 · ClinicalTrials.gov registry record · Phase 2

Safety Study of Botulinum Toxin Type A for the Treatment of Focal Upper Limb Poststroke Spasticity

A Phase 2 study, sponsored by Allergan.

Completed
Registry status
Phase 2
Development phase
279
Enrollment target

NCT00651729: Completed Phase 2 study, sponsored by Allergan.

NCT00651729 is a Phase 2 study that has completed, run by Allergan. The registered enrollment target is 279 participants, above the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (110% higher). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT00651729, a Phase 2 study, has completed, sponsored by Allergan.

COMPLETED
Registry status
Phase 2
Development phase
279 participants
Enrollment target

Study Summary

The purpose of this study is to evaluate the safety of repeated doses of Botulinum Toxin Type A for the treatment of focal upper limb poststroke spasticity

Interventions

  • BIOLOGICAL Botulinum Toxin Type A

Trial Details

FieldValue
Enrollment Target 279 participants
Start Date 2003-04
Est. Completion 2004-12
Phase Phase 2
Allergan

314 total trials

What the finished NCT00651729 record still lists

NCT00651729 is an interventional study that assigns participants to a tested intervention. The registered 279 participants enrollment target is mid-sized for trials with a published cap, above the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (110% higher).

The record links to 0 conditions, and to 1 intervention - of which Botulinum Toxin Type A is the first listed.

NCT00651729 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT00651729 about?

NCT00651729 is a clinical study titled "Safety Study of Botulinum Toxin Type A for the Treatment of Focal Upper Limb Poststroke Spasticity". The purpose of this study is to evaluate the safety of repeated doses of Botulinum Toxin Type A for the treatment of focal upper limb poststroke spasticity

What is the current status of trial NCT00651729?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 279 participants. The study started on 2003-04. Estimated completion is 2004-12.

What interventions are being tested in trial NCT00651729?

The interventions under investigation include: Botulinum Toxin Type A (BIOLOGICAL).

Who is sponsoring clinical trial NCT00651729?

This trial is sponsored by Allergan, which has 314 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT00651729's enrollment target sits among peer trials

279 201st of 2000 higher than 1,799 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 NCT00651729, the US trial registry maintained by the National Library of Medicine. NCT00651729 (mid enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.