Independent directory Public ClinicalTrials.gov records United States
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 Oct 24, 2026, 12:30 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

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

Brief summary

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

This is a study to evaluate the pharmacokinetic (PK) and safety of sonelokimab in adolescent patients with HS.

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

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 30, 2024 (Actual)
Primary completion
Sep 28, 2026 (Estimated)
Completion
Sep 28, 2026 (Estimated)
Last update posted
May 6, 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 6, 2026 · Synced Oct 24, 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 NCT06768671 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →