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Clinical trial

A Phase III, Multicentre, Randomised, Assessor-blind, Parallel Groups, Reference Drug Controlled Study to Assess the Efficacy and Safety of a Single Administration, by Subcutaneous Injection of Dysport® for the Treatment of Hemifacial Spasm

NCT00276315 is registered in ClinicalTrials.gov with Ipsen as lead sponsor.

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Registry record

As filed in ClinicalTrials.gov.

Title
A Phase III, Multicentre, Randomised, Assessor-blind, Parallel Groups, Reference Drug Controlled Study to Assess the Efficacy and Safety of a Single Administration, by Subcutaneous Injection of Dysport® for the Treatment of Hemifacial Spasm
Lead sponsor
Ipsen
Phase
Phase 3
Overall status
Completed
Start date
December 31, 2005
Completion date
January 31, 2007
Enrollment
332 (actual)
Sites
4

Conditions

As the registry lists them; a condition with its own page is linked.