212
Participants
Start Date
April 30, 2014
Primary Completion Date
September 21, 2017
Study Completion Date
September 4, 2018
Botulinum toxin type A
Subjects randomised to receive Dysport 2 U/kg, 8 U/kg or 16 U/kg administered intramuscularly in the study limb.
Aurora
Washington D.C.
New Orleans
Royal Oak
Saint Paul
Omaha
Albuquerque
New York
Columbus
Portland
Austin
Dallas
Brussels
Brno
Prague
Beersheba
Jerusalem
Petah Tikva
Tel Aviv
Tel Litwinsky
La Paz
Celaya
Monterrey
Gdansk
Poznan
Wiązowna
Barcelona
Terrassa
Istanbul
Izmir
Kocaeli
Lead Sponsor
Ipsen
INDUSTRY