Dose-escalating Safety and Preliminary Efficacy of DaxibotulinumtoxinA for Injection in Cervical Dystonia

PHASE2CompletedINTERVENTIONAL
Enrollment

37

Participants

Timeline

Start Date

September 30, 2015

Primary Completion Date

December 7, 2016

Study Completion Date

July 17, 2017

Conditions
Torticollis (Spasmodic)
Interventions
BIOLOGICAL

DaxibotulinumtoxinA

Low, mid, and high dose sequential treatments of daxibotulinumtoxinA in dose-escalation safety and efficacy study

Trial Locations (13)

27157

Wake forest Baptist Health, Winston-Salem

29935

Coastal Neurology, Port Royal

30329

Emory University, Atlanta

32607

University of Florida Center for Movement Disorders & Neurorestoration, Gainesville

33016

Precision Research Organization, Miami Lakes

33613

University of South Florida, Tampa

45212

Riverhills Healthcare, Inc., Cincinnati

60612

Rush University Medical Center, Chicago

66211

Kansas City Bone & Joint Clinic, Overland Park

70810

The NeuroMedical Center Clinic, Baton Rouge

77030

Parkinson's Disease Center and Movement Disorder Clinic, Houston

80907

Colorado Springs Neurological Associates, Colorado Springs

92708

The Parkinson's & Movement Disorder Institute, Fountain Valley

All Listed Sponsors
lead

Revance Therapeutics, Inc.

INDUSTRY

NCT02706795 - Dose-escalating Safety and Preliminary Efficacy of DaxibotulinumtoxinA for Injection in Cervical Dystonia | Biotech Hunter | Biotech Hunter