A Multiple-Dose, Dose-Escalation Study to Evaluate the Safety, Tolerability, and Pharmacokinetics of LY3041658 in Patients with Neutrophilic Skin Diseases
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- STATUS
- Recruiting
Summary
A Multiple-Dose, Dose-Escalation Study to Evaluate the Safety, Tolerability, and Pharmacokinetics of LY3041658 in Patients with Neutrophilic Skin Diseases
Description
Volunteers with neutrophilic skin disease are needed to participate in a research study to assess the safety, tolerability, and activity of an investigational drug that is being developed as a potential treatment for plaque psoriasis, palmoplantar pustulosis, or hidradenitis suppurativa.
Eligible participants will be men and women diagnosed with one of these conditions and are not currently using a biologic agent to treat their skin disease. Participation requires 15 outpatient visits over the course of approximately 15 months. Financial compensation is provided to enrolled participants.
Details
| Condition | Skin Infections/Disorders, Psoriasis and Psoriatic Disorders |
|---|---|
| Clinical Study Identifier | TX147610 |
| Last Modified on | 25 March 2021 |
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Additional screening procedures may be conducted by the study team before you can be confirmed eligible to participate.
Learn moreIf you are confirmed eligible after full screening, you will be required to understand and sign the informed consent if you decide to enroll in the study. Once enrolled you may be asked to make scheduled visits over a period of time.
Learn moreComplete your scheduled study participation activities and then you are done. You may receive summary of study results if provided by the sponsor.
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