drugset / Trial / NCT05277337

Study Comparing Treatment With Alluzience vs Reconstituted Toxin

NCT05277337

Phase 4 Completed 150 enrolled Galderma R&D
RandomizedParallel-groupOpen-labelTreatment

Summary

This is a Phase IV, open-label, randomized, interventional, two-armed, multi-centre study to investigate subject treatment perception and Investigator treatment experience when using Alluzience or vacuum-dried botulinum neurotoxin type A (powder BoNT-A) for treatment of glabellar lines (GL).

Timeline

Start
2022-02-04
Primary completion
2022-10-12
Completion
2022-10-12

Drugs

EvaluationDrugModalityDoseRoute
Subject Alluzience Unknown 50 iu Intramuscular
Comparator Botulinum toxin type A Protein / enzyme biologic 20 iu Intramuscular

Indications

No indication recorded.