Study Condition(s): Psoriasis

A Study of LY3316531 in Healthy Participants and in Participants With Psoriasis

Study Alias: FFAA

Study Identifier(s): Tool Tip Icon {{ defaultRegistry.registryAnchorText }} NCT03418493 {{ currentLocaleObject.registryAnchorText }}

Recruiting Recruiting

Study Purpose

The purpose of this study is to evaluate how well LY3316531 is tolerated and what side effects may occur in healthy participants and participants with psoriasis. The study drug will be administered either subcutaneously (SC) (under the skin) or intravenously (IV) (into a vein in the arm).

Key Participation Requirements Tool Tip Icon

All clinical trials have rules about who can participate. This section outlines some of those rules. Please contact a study center to discuss the full set of criteria

Gender

Male Female

Age

18 years
64 years

Time Commitment

Your participation could last between 16 and 57 weeks.
  • Healthy participants must be between 18 and 64 years old. Participants with psoriasis must be at least 18 years old
  • Participants with psoriasis must have been diagnosed with the disease for at least 6 months and must weigh at least 110 pounds
  • Participants must not have significant uncontrolled disease of a major body organ or system (heart, brain, lungs, blood, liver, kidney, digestive tract, nervous system, etc.)
  • Participants must not have mental health issues
  • Participants must not have had cancer within the last five years, except for certain types of skin cancer
  • Participants must not have had shingles within the last 3 months (participants with psoriasis) or 6 months (healthy participants)
  • Participants with psoriasis must not have taken certain common types of anti-psoriasis medication
  • Female participants must not be pregnant or breastfeeding
  • Participants must be reliable, available and willing to follow study procedures

Where to Participate

2 locations are currently available of 2 planned
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