42
Participants
Start Date
December 31, 2014
Primary Completion Date
March 31, 2016
Study Completion Date
March 31, 2016
Botulinum toxin type A
Subjects to receive Dysport® 500U administered intramuscularly in the targeted upper limb.
Placebo
Placebo administered intramuscularly in the targeted upper limb.
Center for Neurodiagnostic and Therapeutic Services Metropolitan Medical Center, Manila
Department of rehabilitation Medicine Faculty of medicine Siriraj Hospital, Madihol University Hospital, Bangkok
Neurology Laboratory -University Malaya Medical Centre, Kuala Lumpur
TTSH Rehabilitation Centre Ang Mo Kio Community Hospital, Singapore
Lead Sponsor
Ipsen
INDUSTRY