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Completed Phase 3 Interventional Results available

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

ClinicalTrials.gov ID: NCT03014622

Public ClinicalTrials.gov record NCT03014622. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 31, 2026, 5:11 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

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)

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

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

Study identification

NCT ID
NCT03014622
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Revance Therapeutics, Inc.
Industry
Enrollment
303 participants

Conditions and interventions

Interventions

Biological

Eligibility (public fields only)

Age range
18 Years to 75 Years
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Dec 8, 2016 (Actual)
Primary completion
Nov 14, 2017 (Actual)
Completion
Nov 14, 2017 (Actual)
Last update posted
Jul 21, 2022

2016 – 2017

United States locations

U.S. sites
15
U.S. states
10
U.S. cities
14
Facility City State ZIP Site status
Not listed Birmingham Alabama 35205 —
Not listed Beverly Hills California 90210 —
Not listed Newport Beach California 92663 —
Not listed San Francisco California 94117 —
Not listed Santa Monica California 90404 —
Not listed Greenwood Colorado 80111 —
Not listed Boca Raton Florida 33431 —
Not listed Coral Gables Florida 33146 —
Not listed Chestnut Hill Massachusetts 02467 —
Not listed Birmingham Michigan 48009 —
Not listed Montclair New Jersey 07042 —
Not listed New York New York 10001 —
Not listed New York New York 10022 —
Not listed Chapel Hill North Carolina 27517 —
Not listed Nashville Tennessee 37203 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT03014622, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Jul 21, 2022 · Synced Oct 31, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT03014622 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →