Viewing Study NCT03641950


Ignite Creation Date: 2025-12-24 @ 5:04 PM
Ignite Modification Date: 2026-01-04 @ 2:54 AM
Study NCT ID: NCT03641950
Status: COMPLETED
Last Update Posted: 2018-08-22
First Post: 2018-08-19
Is NOT Gene Therapy: True
Has Adverse Events: False

Brief Title: The Objective of This Study is to Evaluate the Efficacy and Safety of Botulax® in Patients With Essential Blepharospasm.
Sponsor: Hugel
Organization:

Study Overview

Official Title: Multi-center, Single Arm, Open-label, Phase IV Clinical Trial to Evaluate the Efficacy and Safety of Botulax® in Patients With Essential Blepharospasm
Status: COMPLETED
Status Verified Date: 2016-03
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: The purpose of this study is evaluate the efficacy and safety of Botulax® in the treatment of Essential blepharospasm.
Detailed Description: Multi-center, single arm, open-label, Phase IV clinical trial to evaluate the efficacy and safety of Botulax® in Subjects with essential blepharospasm

Study Oversight

Has Oversight DMC: True
Is a FDA Regulated Drug?: None
Is a FDA Regulated Device?: None
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: