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Completed Phase 2 Interventional Results available

A Study to Evaluate the Efficacy and Safety of Imsidolimab (ANB019) in Adults With Palmoplantar Pustulosis

ClinicalTrials.gov ID: NCT03633396

Public ClinicalTrials.gov record NCT03633396. 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 Sep 2, 2026, 12:58 PM 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 Phase 2, Randomized, Placebo-controlled, Double-blind, Multiple Dose Study to Evaluate the Efficacy and Safety of ANB019 in Subjects With Palmoplantar Pustulosis

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

A study to evaluate the efficacy and safety, and pharmacokinetic (PK) profile of multiple doses of imsidolimab (ANB019) in adults with palmoplantar pustulosis (PPP)

Study identification

NCT ID
NCT03633396
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Vanda Pharmaceuticals
Industry
Enrollment
59 participants

Conditions and interventions

Interventions

Biological · Drug

Eligibility (public fields only)

Age range
18 Years to 75 Years
Sex
All
Healthy volunteers
Healthy volunteers not accepted

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

Study timeline

Start date
May 19, 2019
Primary completion
Apr 22, 2021
Completion
Apr 22, 2021
Last update posted
Sep 14, 2025

2019 – 2021

United States locations

U.S. sites
19
U.S. states
13
U.S. cities
18
Facility City State ZIP Site status
Investigational Site Birmingham Alabama 35233
Investigational Site Phoenix Arizona 85032
Investigational Site Encino California 91436
Investigational Site Santa Monica California 90405
Investigational Site Fort Lauderdale Florida 33316
Investigational Site Miami Florida 33155
Investigational Site Pembroke Pines Florida 33028
Investigational Site Tampa Florida 33607
Investigational Site Indianapolis Indiana 46250
Investigational Site Plainfield Indiana 46168
Investigational Site Overland Park Kansas 66215
Investigational Site Ann Arbor Michigan 48109
Investigational Site St Louis Missouri 63110
Investigational Site St Louis Missouri 63117
Investigational Site Wilmington North Carolina 28405
Investigational Site Columbus Ohio 43230
Investigational Site Norman Oklahoma 73071
Investigational Site Portland Oregon 97239
Investigational Site Dallas Texas 75230

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

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 20 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT03633396, 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 Sep 14, 2025 · Synced Sep 2, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT03633396 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →