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Completed Phase 2 Interventional

Evaluation of Sonelokimab for the Treatment of Patients With Active Moderate to Severe Hidradenitis Suppurativa

ClinicalTrials.gov ID: NCT05322473

Public ClinicalTrials.gov record NCT05322473. 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 5, 2026, 9:39 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

Phase 2, Randomized, Parallel-group, Double-blind, Placebo-controlled Study of Sonelokimab in Patients 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 demonstrate the clinical efficacy and safety of the nanobody® sonelokimab administered subcutaneously (sc) compared with placebo in the treatment of adult participants with moderate to severe hidradenitis suppurativa.

Study identification

NCT ID
NCT05322473
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
MoonLake Immunotherapeutics AG
Industry
Enrollment
234 participants

Conditions and interventions

Interventions

Drug · Other

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
Apr 24, 2022
Primary completion
May 8, 2023
Completion
Aug 29, 2023
Last update posted
May 2, 2024

2022 – 2023

United States locations

U.S. sites
15
U.S. states
10
U.S. cities
15
Facility City State ZIP Site status
Clinical Site Fountain Valley California 92708
Clinical Site Los Angeles California 90056
Clinical Site Miami Florida 33136
Clinical Site Ormond Beach Florida 32127
Clinical Site St. Petersburg Florida 33709
Clinical Site Tampa Florida 33613
Clinical Site Indianapolis Indiana 46250
Clinical Site Beverly Massachusetts 01915
Clinical Site Boston Massachusetts 02215
Clinical Site Omaha Nebraska 68144
Clinical Site New York New York 10003
Clinical Site Philadelphia Pennsylvania 19103
Clinical Site Charleston South Carolina 29425
Clinical Site Nashville Tennessee 37215
Clinical Site Bellaire Texas 77401

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 42 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT05322473, 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 2, 2024 · Synced Sep 5, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT05322473 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →