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Completed Phase 2 Interventional Results available

A Study to Evaluate the Efficacy, Safety, and Tolerability of Guselkumab for the Treatment of Participants With Moderate to Severe Hidradenitis Suppurativa (HS)

ClinicalTrials.gov ID: NCT03628924

Public ClinicalTrials.gov record NCT03628924. 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 12, 2026, 2:20 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 2, Multicenter, Randomized, Placebo-Controlled, Double-Blind, Proof-of-Concept Study to Evaluate Guselkumab for the Treatment of Subjects With Moderate to Severe Hidradenitis Suppurativa

Study identification

NCT ID
NCT03628924
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Janssen Research & Development, LLC
Industry
Enrollment
184 participants

Conditions and interventions

Interventions

  • Guselkumab dose 1 Drug
  • Guselkumab dose 2 Drug
  • Guselkumab dose 3 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
Sep 3, 2018
Primary completion
May 21, 2020
Completion
May 21, 2020
Last update posted
Feb 3, 2025

2018 – 2020

United States locations

U.S. sites
20
U.S. states
14
U.S. cities
17
Facility City State ZIP Site status
University of Alabama Birmingham Birmingham Alabama 35233
Olympian Clinical Research Largo Florida 33770
Renstar Medical Research Ocala Florida 34470
Park Avenue Dermatology Orange Park Florida 32073
Olympian Clinical Research Tampa Florida 33614
Forcare Clinical Research Inc Tampa Florida 33624
Great Lakes Clinical Trials Chicago Illinois 60640
Indiana Clinical Trial Center Plainfield Indiana 46168
Tufts Medical Center Boston Massachusetts 02111
Massachusetts General Hospital Boston Massachusetts 02114
Beth Israel Deaconess Medical Center Boston Massachusetts 02215
Hamzavi Dermatology Fort Gratiot Michigan 48059
Central Dermatology St Louis Missouri 63117
Clinical Studies Group Henderson Nevada 89052
Ohio State University Columbus Ohio 43215
Oregon Medical Research Center Portland Oregon 97223
University of Pittsburgh Department of Dermatology Pittsburgh Pennsylvania 15213
Clinical Partners, LLC Johnston Rhode Island 02919
Progressive Clinical Research San Antonio Texas 78213
Dermatology Associates of Seattle Seattle Washington 98101-1498

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 25 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT03628924, 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 Feb 3, 2025 · Synced May 12, 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 NCT03628924 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →