drugset / Trial / NCT00702754

Open Label Safety/Immunogenicity Study of MYOBLOC (Neurobloc; Botulinum Toxin Type B) in Patients With Cervical Dystonia

NCT00702754

NaSingle-groupOpen-labelTreatment

Summary

Open label study to evaluate the safety and immunogenicity of MYOBLOC (Botulinum Toxin Type B) in adult patients with a clinical diagnosis of Cervical Dystonia (CD).

Timeline

Start
2001-06
Primary completion
2008-05
Completion
2008-09

Drugs

EvaluationDrugModalityDoseRoute
Subject Botulinum Toxin Type B Unknown 5000 iu
Subject Botulinum Toxin Type B Unknown 25000 iu

Indications