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Enrolling by invitation Phase 3 Interventional

A Study to Evaluate the Long-term Safety, Tolerability, and Efficacy of Subcutaneous Sonelokimab in Participants With Moderate to Severe Hidradenitis Suppurativa

ClinicalTrials.gov ID: NCT07007637

Public ClinicalTrials.gov record NCT07007637. 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 28, 2026, 6:10 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, Multicenter, Open-label Extension Study to Evaluate the Long-term Safety, Tolerability, and Efficacy of Subcutaneous Sonelokimab in Participants With Moderate to Severe Hidradenitis Suppurativa

Brief summary

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

This is a study to evaluate the long-term safety, tolerability, and efficacy of sonelokimab in participants with moderate to severe hidradenitis suppurativa who were previously enrolled in a parental study.

Study identification

NCT ID
NCT07007637
Recruitment status
Enrolling by invitation
Study type
Interventional
Phase
Phase 3
Lead sponsor
MoonLake Immunotherapeutics AG
Industry
Enrollment
835 participants

Conditions and interventions

Interventions

Drug

Eligibility (public fields only)

Age range
12 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
Jun 27, 2025 (Actual)
Primary completion
Jun 13, 2028 (Estimated)
Completion
Jun 13, 2028 (Estimated)
Last update posted
Jun 8, 2026

2025 – 2028

United States locations

U.S. sites
49
U.S. states
23
U.S. cities
43
Facility City State ZIP Site status
Clinical Site Birmingham Alabama 35244 —
Clinical Site North Little Rock Arkansas 72117 —
Clinical Site Los Angeles California 90404 —
Clinical Site Northridge California 91325 —
Clinical Site Aventura Florida 33180 —
Clinical Site Coral Gables Florida 33134 —
Clinical Site Hialeah Florida 33012 —
Clinical Site Hollywood Florida 33021-6746 —
Clinical Site Miami Florida 33136 —
Clinical Site Miami Florida 33163 —
Clinical Site Ocala Florida 34471 —
Clinical Site Tampa Florida 33607 —
Clinical Site Tampa Florida 33613 —
Clinical Site Macon Georgia 31217 —
Clinical Site Sandy Springs Georgia 30328 —
Clinical Site Skokie Illinois 60077 —
Clinical Site West Dundee Illinois 60118 —
Clinical Site Columbus Indiana 47201 —
Clinical Site New Albany Indiana 47150 —
Clinical Site Plainfield Indiana 46168 —
Clinical Site Louisville Kentucky 40241 —
Clinical Site Murray Kentucky 42071 —
Clinical Site Metairie Louisiana 70006 —
Clinical Site Boston Massachusetts 02116 —
Clinical Site Boston Massachusetts 02215 —
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 89148 —
Clinical Site New York New York 10003 —
Clinical Site New York New York 10012 —
Clinical Site The Bronx New York 10467 —
Clinical Site Fargo North Dakota 58103 —
Clinical Site Boardman Ohio 44512 —
Clinical Site Columbus Ohio 43213 —
Clinical Site Dayton Ohio 45324 —
Clinical Site Oklahoma City Oklahoma 73118 —
Clinical Site Murfreesboro Tennessee 37130 —
Clinical Site Dallas Texas 75235 —
Clinical Site Dallas Texas 75246 —
Clinical Site Houston Texas 77004 —
Clinical Site San Antonio Texas 78213 —
Clinical Site San Antonio Texas 78218 —
Clinical Site South Jordan Utah 84095 —
Clinical Site Mill Creek Washington 98012 —
Clinical Site Morgantown West Virginia 26505 —

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 117 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT07007637, 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 8, 2026 · Synced Oct 28, 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 NCT07007637 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →