Study Condition(s): Psoriasis

A Study Comparing Different Dosing Regimens of Ixekizumab (LY2439821) in Participants With Moderate to Severe Plaque Psoriasis (IXORA-P)

Study Alias: RHBP

Study Identifier(s): Tool Tip Icon {{ defaultRegistry.registryAnchorText }} NCT02513550 {{ currentLocaleObject.registryAnchorText }}

Completed Completed

Study Purpose

The main purpose of this study is to evaluate the efficacy of ixekizumab dosing regimens in participants with plaque psoriasis

Completed Study

The results of this study are not yet available.

Who Participated? Tool Tip Icon

Here you can find out a bit more about the requirements for volunteers who took part in this study

Gender

Male Female

Age

18+ years

Time Commitment

Your participation could last up to 80 weeks and include approximately 18 visits to the study center
  • Participant must have chronic plaque psoriasis for at least 6 months before the start of the study

  • Participant must not have received phototherapy and/or systemic therapyfor at least 4 weeks prior to enrollment

  • Participant must agree to use reliable method of birth control during the study; women must continue using birth control for at least 12 weeks after stopping study treatment

  • Participant must be willing to avoid excessive sun exposure or use of tanning booths for at least 4 weeks prior to enrollment and during the study

  • Participant must not be currently taking or have recently used any biologic agent

  • Participant must not have evidence of tuberculosis, major surgery within 8 weeks of baseline or require surgery during the study

  • Female participant must not be pregnant or breastfeeding

Where This Study Took Place Tool Tip Icon

138 locations participated
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