Safety and Efficacy of NABOTA in Treatment of Essential Blepharospasm
NCT02947815 · Status: COMPLETED · Phase: PHASE2/PHASE3 · Type: INTERVENTIONAL · Enrollment: 234
Last updated 2019-06-26
Summary
The purpose of this study is to evaluate the Efficacy and Safety of NABOTA in treatment of essential blepharospasm
Conditions
- Blepharospasm
Interventions
- DRUG
-
Clostridium Botulinum Toxin Type A
- DRUG
-
Clostridium Botulinum Toxin Type A
Sponsors & Collaborators
-
Daewoong Pharmaceutical Co. LTD.
lead INDUSTRY
Study Design
- Allocation
- RANDOMIZED
- Purpose
- TREATMENT
- Masking
- DOUBLE
- Model
- PARALLEL
Eligibility
- Min Age
- 18 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2016-10-31
- Primary Completion
- 2018-01-31
- Completion
- 2018-01-31
Countries
- South Korea
Study Locations
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