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Completed Phase 1 Interventional Accepts healthy volunteers

A Study to Evaluate the Pharmacokinetics, Safety and Tolerability of ABBV-157 in Healthy Volunteers and in Participants With Chronic Plaque Psoriasis

ClinicalTrials.gov ID: NCT03922607

Public ClinicalTrials.gov record NCT03922607. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced May 17, 2026, 3:33 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Randomized, Double-Blind, Placebo-Controlled, Multiple-Dose Study to Evaluate the Pharmacokinetics, Safety and Tolerability of ABBV-157 in Healthy Volunteers and in Subjects With Chronic Plaque Psoriasis

Study identification

NCT ID
NCT03922607
Recruitment status
Completed
Study type
Interventional
Phase
Phase 1
Lead sponsor
AbbVie
Industry
Enrollment
65 participants

Conditions and interventions

Conditions

Interventions

  • ABBV-157 Drug
  • Placebo for ABBV-157 Drug

Drug

Eligibility (public fields only)

Age range
18 Years to 75 Years
Sex
All
Healthy volunteers
Accepts healthy volunteers

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Jun 10, 2019
Primary completion
Apr 12, 2021
Completion
Apr 12, 2021
Last update posted
May 10, 2021

2019 – 2021

United States locations

U.S. sites
10
U.S. states
7
U.S. cities
10
Facility City State ZIP Site status
Total Skin and Beauty Derm Ctr /ID# 222593 Birmingham Alabama 35205
Alliance Dermatology and MOHs /ID# 222622 Phoenix Arizona 85032
Anaheim Clinical Trials LLC /ID# 213645 Anaheim California 92801-2658
Dermatology Res. Assoc., CA /ID# 224980 Los Angeles California 90045
Providence Clinical Research /ID# 213339 North Hollywood California 91606
Advanced Medical Research /ID# 216090 Sandy Springs Georgia 30328-6141
Acpru /Id# 213639 Grayslake Illinois 60030
University of Pittsburgh MC /ID# 224699 Pittsburgh Pennsylvania 15260
PPD PH I Clinical Unit /ID# 213062 Austin Texas 78744
Center for Clinical Studies - Webster TX /ID# 217352 Webster Texas 77598

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT03922607, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted May 10, 2021 · Synced May 17, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT03922607 live on ClinicalTrials.gov.

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