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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 Oct 18, 2026, 12:30 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 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 20, 2019 (Actual)
Primary completion
Apr 23, 2021 (Actual)
Completion
Apr 23, 2021 (Actual)
Last update posted
Sep 15, 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 15, 2025 · Synced Oct 18, 2026

Related: full search, browse by condition, browse by drug or therapy, browse by sponsor, browse by U.S. city.

Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT03633396 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →