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Completed Phase 4 Interventional Results available

Open-Label Non-Inferiority Study Evaluating the Efficacy and Safety of Xeomin® in Subjects With Cervical Dystonia Flex

ClinicalTrials.gov ID: NCT01486264

Public ClinicalTrials.gov record NCT01486264. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 29, 2026, 12:17 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

An Open-Label, Non-Inferiority Study Evaluating the Efficacy and Safety of Two Injection Schedules of Xeomin® (incobotulinumtoxinA) [Short Flex Versus Long Flex] in Subjects With Cervical Dystonia With < 10 Weeks of Benefit From OnabotulinumtoxinA Treatment

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

This study will compare Xeomin®, a botulinum toxin medication, in shorter treatment intervals (Short Flex dosing) to the standard interval dosing (Long Flex dosing) to determine if the response to treatment is comparable in both how it works and any side effects. Xeomin® is approved by the United States Food and Drug Administration (FDA) for the treatment of cervical dystonia (CD). The use of Xeomin® is investigational in regards to shorter treatment intervals. An investigational use is one that is not approved by the FDA.

Study identification

NCT ID
NCT01486264
Recruitment status
Completed
Study type
Interventional
Phase
Phase 4
Lead sponsor
Merz Pharmaceuticals GmbH
Industry
Enrollment
283 participants

Conditions and interventions

Interventions

Biological

Eligibility (public fields only)

Age range
18 Years to 81 Years
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Jan 20, 2012 (Actual)
Primary completion
Mar 29, 2016 (Actual)
Completion
Mar 29, 2016 (Actual)
Last update posted
Oct 27, 2022

2012 – 2016

United States locations

U.S. sites
43
U.S. states
22
U.S. cities
37
Facility City State ZIP Site status
Merz Investigative Site #001234 Birmingham Alabama 35294-0017 —
Merz Investigative Site 001017 Fountain Valley California 92708 —
Merz Investigative Site #001225 Loma Linda California 92354-3450 —
Merz Investigative Site #001219 Los Angeles California 90033 —
Merz Investigative Site # 001276 Manchester Connecticut 06040 —
Merz Investigative Site #001231 Washington D.C. District of Columbia 20007 —
Merz Investigative Site #001076 Boca Raton Florida 33486 —
Merz Investigative Site #001019 Gainesville Florida 32610 —
Merz Investigative Site #001046 Jacksonville Florida 32209 —
Merz Investigative Site #001075 Melbourne Florida 32901 —
Merz Investigative Site #001217 Port Charlotte Florida 33980 —
Merz Investigative Site #1253 Tampa Florida 33613 —
Merz Investigative Site #001055 Atlanta Georgia 30329 —
Merz Investigative Site# 01255 Chicago Illinois 60611 —
Merz Investigative Site #001215 Chicago Illinois 60612 —
Merz Investigative Site # 01069 Des Moines Iowa 50309 —
Merz Investigative Site #001110 Overland Park Kansas 66211 —
Merz Investigative Site # 001071 Elkridge Maryland 21075 —
Merz Investigative Site # 001018 Detroit Michigan 48201-2153 —
Merz Investigative Site #001030 Farmington Hills Michigan 48334 —
Merz Investigative Site # 0001275 Eagan Minnesota 55121 —
Merz Investigative Site #1250 St Louis Missouri 63104 —
Merz Investigative Site #001210 St Louis Missouri 63110 —
Merz Investigative Site #001221 Albany New York 12208 —
Merz Investigative Site #001233 New York New York 10003 —
Merz Investigative Site #1256 New York New York 10029-6574 —
Merz Investigative Site# 01252 Charlotte North Carolina 28207 —
Merz Investigative Site #001005 Durham North Carolina 27705 —
Merz Investigative Site# 01260 Raleigh North Carolina 27607 —
Merz Investigative Site #001009 Winston-Salem North Carolina 27157 —
Merz Investigative Site #1265 Cincinnati Ohio 45219 —
Merz Investigative Site #001220 Tulsa Oklahoma 74136 —
Merz Investigative Site #1033 Portland Oregon 97239 —
Merz Investigative Site #1251 Portland Oregon 97239 —
Merz Investigative Site # 0001271 Hershey Pennsylvania 17033 —
Merz Investigative Site #1249 Philadelphia Pennsylvania 19107 —
Merz Investigative Site #001206 Nashville Tennessee 37232-2551 —
Merz Investigative Site #1074 Dallas Texas 75214 —
Merz Investigative Site #001223 Dallas Texas 75231 —
Merz Investigative Site # 001216 Houston Texas 77030 —
Merz Investigative Site# 001266 Houston Texas 77030 —
Merz Investigative Site #001224 Kirkland Washington 98034 —
Merz Investigative Site #1270 Seattle Washington 98122 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT01486264, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Oct 27, 2022 · Synced Oct 29, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT01486264 live on ClinicalTrials.gov.

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