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A Phase 1, Double-Blind, Randomized, Placebo-Controlled, Multiple-Dose Study to Evaluate the Safety, Tolerability, and Pharmacokinetics of Subcutaneous LY3471851 in Patients With Psoriasis
The main purpose of this study is to learn more about the safety of LY3471851 when given by injection just under the skin to participants with psoriasis. The study will last up to 48 weeks and may include up to 23 visits to the study center.
Age
18 - 70 years
Sex
ALL
Healthy Volunteers
No
Arkansas Research Trials, LLC
North Little Rock, Arkansas, United States
California Dermatology & Clinical Research Institute
Encinitas, California, United States
Center For Dermatology Clinical Research, Inc.
Fremont, California, United States
Therapeutics Clinical Research
San Diego, California, United States
Clinical Science Institute
Santa Monica, California, United States
Florida Academic Centers Research and Education, LLC
Coral Gables, Florida, United States
Miami Dermatology and Laser Research
Miami, Florida, United States
ForCare Clinical Research
Tampa, Florida, United States
Medical Dermatology Specialists
Sandy Springs, Georgia, United States
Dawes Fretzin Clinical Research Group, LLC
Indianapolis, Indiana, United States
Start Date
November 26, 2019
Primary Completion Date
July 21, 2021
Completion Date
July 21, 2021
Last Updated
February 20, 2024
30
ACTUAL participants
Placebo
DRUG
LY3471851
DRUG
Lead Sponsor
Nektar Therapeutics
Collaborators
NCT07449234
NCT07116967
NCT07250802
Data Source & Attribution
This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.
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