Clinical Trials Directory

Trials / Completed

CompletedNCT03014622

Efficacy and Safety of DaxibotulinumtoxinA for Injection to Treat Moderate to Severe Glabellar Lines

A Phase 3, Randomized, Double-Blind, Placebo Controlled, Multi-Center Trial to Evaluate the Efficacy and Safety of DaxibotulinumtoxinA for Injection to Treat Moderate to Severe Glabellar Lines (SAKURA-1)

Status
Completed
Phase
Phase 3
Study type
Interventional
Enrollment
303 (actual)
Sponsor
Revance Therapeutics, Inc. · Industry
Sex
All
Age
18 Years – 75 Years
Healthy volunteers
Not accepted

Summary

This is a safety and efficacy study of DaxibotulinumtoxinA for Injection to treat moderate to severe frown lines.

Conditions

Interventions

TypeNameDescription
BIOLOGICALBotulinum Toxins, Type AIntramuscular injection
BIOLOGICALPlacebosIntramuscular injection

Timeline

Start date
2016-12-08
Primary completion
2017-11-14
Completion
2017-11-14
First posted
2017-01-09
Last updated
2022-07-21
Results posted
2022-07-21

Locations

15 sites across 1 country: United States

Source: ClinicalTrials.gov record NCT03014622. Inclusion in this directory is not an endorsement.

Efficacy and Safety of DaxibotulinumtoxinA for Injection to Treat Moderate to Severe Glabellar Lines (NCT03014622) · Clinical Trials Directory