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CompletedNCT00515944Updated Apr 1, 2009

Evaluate the Migration Potential of Xeomin® Compared to Two Other Botulinum Toxin Type A Products

A Phase 1 interventional study of Botulinum neurotoxin type A, free of complexing proteins in Healthy, sponsored by Merz Pharmaceuticals GmbH. Completed at 1 site in Germany. Open to female participants aged 18 Years to 65 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2009-04-01.

Sponsored by Merz Pharmaceuticals GmbH · Phase 1 and Interventional

Phase
Phase 1
Study type
Interventional
Enrollment
30
Allocation
Randomized
Ages
18 Years to 65 Years
Sex
Female
01

Study summary

Xeomin® is a Botulinum neurotoxin type A preparation free of complexing proteins, i.e. free of bacterial proteins other than the active toxin. Injected into the muscle, Xeomin® causes local weakening. Botulinum toxin type A is used for certain neurological and aesthetic treatments. This study will investigate the migration potential of Xeomin®.

Read the detailed description

Conducted in Europe

02

Conditions studied

  • Healthy

Keywords

  • No condition
  • healthy volunteers
03

In context

Lead sponsor

Merz Pharmaceuticals GmbH is the lead sponsor of 60 studies on the registry; none are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 65 Years
Sexes eligible
Female
Accepts healthy volunteers
Yes

Eligibility criteria

Inclusion Criteria:

  • Healthy females, 18 to 65 years
05

Study design

Phase
Phase 1
Allocation
Randomized
Intervention model
Single group
Masking
Double
Enrollment
30 participants (estimated)

Interventions

  • DrugBotulinum neurotoxin type A, free of complexing proteins
06

What researchers measure

Primary outcomes

  1. Measurement of area

07

Study locations

1 site
  • Merz Pharmaceuticals GmbH
    Frankfurt am Main, 61273, Germany
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Apr 1, 2009, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT00515944
Lead sponsor
Merz Pharmaceuticals GmbH
First posted
Aug 14, 2007
Start date
Aug 2007
Primary completion
Feb 2008
Completion
Jun 2008
Last update
Apr 1, 2009

Study contacts

Merz Pharmaceuticals
study chair · Merz Pharmaceuticals GmbH
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Mar 2009. You cannot join it, but the record below documents what was studied.

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