ClinicalTrials.gov record
Active, not recruiting Phase 3 Interventional

An Open-label, Single-arm Study to Evaluate Pharmacokinetics and Safety of Subcutaneous Sonelokimab in Adolescents With Moderate to Severe Hidradenitis Suppurativa (VELA-TEEN)

ClinicalTrials.gov ID: NCT06768671

Public ClinicalTrials.gov record NCT06768671. 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 May 7, 2026, 9:03 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

An Open-label, Single-arm Study to Evaluate the Pharmacokinetics and Safety of Subcutaneous Sonelokimab in Adolescents Aged ≥12 to ≤17 Years at the Time of Study Inclusion With Active Moderate to Severe Hidradenitis Suppurativa

Study identification

NCT ID
NCT06768671
Recruitment status
Active, not recruiting
Study type
Interventional
Phase
Phase 3
Lead sponsor
MoonLake Immunotherapeutics AG
Industry
Enrollment
35 participants

Conditions and interventions

Interventions

  • Sonelokimab Drug

Drug

Eligibility (public fields only)

Age range
12 Years to 17 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
Dec 29, 2024
Primary completion
Sep 27, 2026
Completion
Sep 27, 2026
Last update posted
May 5, 2026

2024 – 2026

United States locations

U.S. sites
18
U.S. states
14
U.S. cities
17
Facility City State ZIP Site status
Clinical Site North Little Rock Arkansas 72117
Clinical Site Stanford California 94304
Clinical Site Washington D.C. District of Columbia 20010
Clinical Site Hollywood Florida 33201
Clinical Site Miami Florida 33136
Clinical Site Macon Georgia 31217
Clinical Site Sandy Springs Georgia 30328
Clinical Site Chicago Illinois 60611
Clinical Site Columbus Indiana 47201
Clinical Site Murray Kentucky 42071
Clinical Site Waterford Michigan 48328
Clinical Site Fargo North Dakota 58103
Clinical Site Charleston South Carolina 29425
Clinical Site Dallas Texas 75246
Clinical Site Dallas Texas 75390-8575
Clinical Site San Antonio Texas 78218
Clinical Site Norfolk Virginia 23502
Clinical Site Seattle Washington 98105

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

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT06768671, 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 May 5, 2026 · Synced May 7, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT06768671 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →