A Study of LY3041658 in Participants With Skin Diseases
Completed · Phase 1 · Has a placebo group
Conditions studied: Skin Diseases, Psoriasis
In brief
The main purpose of this study is to investigate the safety and tolerability of the study drug known as LY3041658 in participants with certain types of skin diseases. The study will measure how the body absorbs, breaks down and gets rid of LY3041658. It will last about 127 days for each participant, not including screening. This study is for research purposes only, and is not intended to treat any medical condition.
Key facts
- Study ID
- NCT02896868
- Run by
- Eli Lilly and Company
- People needed
- 60
- Starts
- 2016-11-08
- Expected to finish
- 2019-03-19
- Last updated by the study team
- 2019-05-03
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Investigator confirmed diagnosis of certain skin diseases for at least 6 months.
- Active skin lesions that are not responding to standard therapies.
- Willing to undergo pre- and post-treatment skin biopsies of lesions.
You may not qualify if…
- Have other skin diseases that may interfere with evaluation of the specified skin disease being studied.
Where it is running
- Parexel Early Phase Unit at Glendale — Glendale, California, United States
- Dawes Fretzin Clinical Research — Indianapolis, Indiana, United States
- PAREXEL-Phase 1 Baltimore Harbor Hospital Center — Baltimore, Maryland, United States
- Duke University Medical Center — Durham, North Carolina, United States
- Altoona Center for Clinical Research — Duncansville, Pennsylvania, United States
Full record on ClinicalTrials.gov
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