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Completed Phase 2 Interventional Results available

A Study to Evaluate the Efficacy and Safety of Imsidolimab (ANB019) in the Treatment of Participants With Hidradenitis Suppurativa

ClinicalTrials.gov ID: NCT04856930

Public ClinicalTrials.gov record NCT04856930. 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, 4:59 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, Double-Blind, Placebo Controlled Study to Evaluate the Efficacy and Safety of Imsidolimab (ANB019) in the Treatment of Subjects With Hidradenitis Suppurativa

Brief summary

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

Efficacy and safety of imsidolimab (ANB019) in participants with Hidradenitis Suppurativa

Study identification

NCT ID
NCT04856930
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Vanda Pharmaceuticals
Industry
Enrollment
149 participants

Conditions and interventions

Interventions

Biological

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
Jul 6, 2021
Primary completion
Jul 14, 2022
Completion
Dec 13, 2022
Last update posted
Sep 21, 2025

2021 – 2022

United States locations

U.S. sites
17
U.S. states
11
U.S. cities
17
Facility City State ZIP Site status
Site 10-108 Birmingham Alabama 35224
Site 10-104 Fountain Valley California 92708
Site 10-119 Northridge California 91324
Site 10-102 Sacramento California 95817
Site 10-109 Coral Gables Florida 33134
Site 10-107 Largo Florida 33770
Site 10-111 Tampa Florida 33607
Site 10-110 Sandy Springs Georgia 30328
Site 10-101 Fort Gratiot Michigan 48059
Site 10-103 Portsmouth New Hampshire 03801
Site 10-115 Warwick Rhode Island 02886
Site 10-113 Greenville South Carolina 29615
Site 10-118 Houston Texas 77056
Site 10-112 Pflugerville Texas 78660
Site 10-117 San Antonio Texas 78213
Site 10-105 Norfolk Virginia 23502
Site 10-106 Spokane Washington 99202

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 17 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT04856930, 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 21, 2025 · Synced Sep 2, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT04856930 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →