drugset / Trial / NCT03014622

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

NCT03014622 ↗

Phase 3 Completed 303 enrolled Revance Therapeutics, Inc.
RandomizedParallel-groupTriple-blindTreatment

Summary

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

Timeline

Start
2016-12-08
Primary completion
2017-11-14
Completion
2017-11-14

Outcome

Met primary endpoint

paper DAXI was significantly more effective than placebo in achieving the primary efficacy outcome PMID 31609882 ↗

paper 73.6 percent versus 0.0 percent (SAKURA 1), and 74.0 percent versus 1.0 percent (SAKURA 2) (both p < 0.0001). PMID 31609882 ↗

Drugs

EvaluationDrugModalityDoseRoute
Subject Botulinum toxin type A Protein / enzyme biologic 40 iu Intramuscular

Indications

No indication recorded.