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Completed Phase 3 Interventional

Study to Evaluate the Efficacy and Safety of Subcutaneous Sonelokimab Compared With Placebo in Adult Participants With Moderate to Severe Hidradenitis Suppurativa

ClinicalTrials.gov ID: NCT06411379

Public ClinicalTrials.gov record NCT06411379. 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 Jul 23, 2026, 4:19 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 3, Randomized, Double-blind, Placebo-controlled, Multicenter Study to Evaluate the Efficacy and Safety of Subcutaneous Sonelokimab in Adult Participants With Moderate to Severe Hidradenitis Suppurativa

Study identification

NCT ID
NCT06411379
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
MoonLake Immunotherapeutics AG
Industry
Enrollment
418 participants

Conditions and interventions

Interventions

  • Sonelokimab Drug
  • Placebo Drug

Drug

Eligibility (public fields only)

Age range
18 Years and older
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 13, 2024
Primary completion
Aug 13, 2025
Completion
May 19, 2026
Last update posted
Jun 7, 2026

2024 – 2026

United States locations

U.S. sites
30
U.S. states
20
U.S. cities
30
Facility City State ZIP Site status
Clinical Site Birmingham Alabama 35244
Clinical Site North Little Rock Arkansas 72117
Clinical Site Fountain Valley California 92708
Clinical Site Santa Monica California 90404
Clinical Site Aventura Florida 33180
Clinical Site Hialeah Florida 33012
Clinical Site Miami Florida 33136
Clinical Site Ocala Florida 34470
Clinical Site Tampa Florida 33613
Clinical Site Skokie Illinois 60077
Clinical Site Plainfield Indiana 46168
Clinical Site Murray Kentucky 42071
Clinical Site Baton Rouge Louisiana 70809
Clinical Site Baltimore Maryland 21287
Clinical Site Ann Arbor Michigan 48109-5314
Clinical Site Canton Michigan 48187
Clinical Site Clarkston Michigan 48346
Clinical Site Waterford Michigan 48328
Clinical Site New Brighton Minnesota 55112
Clinical Site Omaha Nebraska 68144
Clinical Site Las Vegas Nevada 89145
Clinical Site New York New York 10003
Clinical Site Fargo North Dakota 58103
Clinical Site Columbus Ohio 43213
Clinical Site Murfreesboro Tennessee 37130
Clinical Site Dallas Texas 75390-8565
Clinical Site Plano Texas 75025
Clinical Site San Antonio Texas 78213
Clinical Site Morgantown West Virginia 26505
Clinical Site Milwaukee Wisconsin 53226

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 76 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT06411379, 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 Jun 7, 2026 · Synced Jul 23, 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 protocol, eligibility criteria, and contact information for NCT06411379 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →