drugset / Trial / NCT03485976

Ixekizumab in the Treatment of Pityriasis Rubra Pilaris (PRP)

NCT03485976

NaSingle-groupOpen-labelTreatment

Summary

15 patients with PRP will be treated with ixekizumab for 24 weeks to determine safety and efficacy. Participants are required to travel to Portland, OR only for the first visit and week-24 visit. 5 visits in between these times and one follow up visit may be performed by secure videoconferencing.

Timeline

Start
2018-05-23
Primary completion
2019-10-14
Completion
2020-01-13

Drugs

EvaluationDrugModalityDoseRoute
Subject Ixekizumab Monoclonal antibody 80 mg Subcutaneous