A Study to Compare the Safety and Efficacy of Dysport® and Botox® in Adults With Upper Limb Spasticity.

Last updated:
2026-07-18
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View trial details

Overview

Official protocol title:

A MULTICENTRE, INTERVENTIONAL, POST-MARKETING, RANDOMISED, DOUBLE-BLIND, CROSSOVER STUDY TO EVALUATE THE CLINICAL SAFETY AND EFFICACY OF ABOBOTULINUMTOXINA (DYSPORT) IN COMPARISON WITH ONABOTULINUMTOXINA (BOTOX) WHEN TREATING ADULTS WITH UPPER LIMB SPASTICITY

Intervention/treatment:
DYSPORT THERAPEUTIC / BOTOX
Medical condition:
LIMB SPASTICITY
Protocol code:
CLIN-52120-452
Control number:
254845
Status:
Closed
Approved:
September 02, 2021
Date Completed:
Trial phase:
Phase 4
For more information:
ClinicalTrials.gov - NCT04936542
This is an external link. The information is not authorized by the Government of Canada.

Eligibility

Sex: ALL
Age
18 Years to 80 Years
Accepts healthy volunteers: No

Contacts and locations

Contact
Name
Medical Director
Organization
Ipsen
Phone:
see email
Sponsor
IPSEN PHARMA

Locations

Genge Partners
Montreal, H3A 2B4
Victoria General Hospital
Victoria, V9A 3P2

Ontario

Lawson Health Research Institute
London, Ontario, N6C 5J1
Moncton Hospital
Moncton, Ontario, E1C 6Z8

Results

See the results from the trial NCT04936542. This is an external link. The information is not authorized by the Government of Canada.

Date posted:
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