drugset / Trial / NCT02568111

Brimonidine Tartrate for the Treatment of Injection Related Erythema

NCT02568111

Phase 4 Withdrawn Biogen
RandomizedParallel-groupTriple-blindSupportive care

Summary

The primary objective of this study is to evaluate the Injection Related Erythema (IRE) mitigation effect of a single administration of brimonidine tartrate in comparison with a vehicle gel (placebo). The secondary study objectives are to evaluate the IRE mitigation effect of a single administration of brimonidine tartrate in comparison with a vehicle gel on a more stringent definition scale, in accordance with the primary endpoint of the original brimonidine pivotal trials and participants' satisfaction with the overall appearance of their skin.

Timeline

Start
2016-02
Primary completion
2016-08
Completion
2016-08

Drugs

EvaluationDrugModalityDoseRoute
Subject Brimonidine Small molecule Topical
Background peginterferon beta-1a Protein / enzyme biologic 125 ug Subcutaneous