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Terminated Phase 2 Interventional

A Study of the Efficacy and Safety of Brensocatib in Adults With Moderate to Severe Hidradenitis Suppurativa (HS)

ClinicalTrials.gov ID: NCT06685835

Public ClinicalTrials.gov record NCT06685835. 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 2, 2026, 11:10 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

A Phase 2b, Randomized, Double-Blind, Placebo-Controlled, Multicenter Study of the Efficacy and Safety of Brensocatib in Adults With Moderate to Severe Hidradenitis Suppurativa - The CEDAR Study

Brief summary

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

The primary purpose of the study is to evaluate the effect of brensocatib compared with placebo.

Study identification

NCT ID
NCT06685835
Recruitment status
Terminated
Study type
Interventional
Phase
Phase 2
Lead sponsor
Insmed Incorporated
Industry
Enrollment
214 participants

Conditions and interventions

Interventions

Drug

Eligibility (public fields only)

Age range
18 Years to 80 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 15, 2024
Primary completion
Feb 11, 2026
Completion
Jun 7, 2026
Last update posted
Jun 28, 2026

2024 – 2026

United States locations

U.S. sites
26
U.S. states
15
U.S. cities
25
Facility City State ZIP Site status
USA001 Phoenix Arizona 85054-4502
USA007 Sacramento California 95815
USA026 Coral Gables Florida 33134
USA027 Hollywood Florida 33024
USA021 Margate Florida 33063
USA018 Miami Florida 33125
USA025 Ocala Florida 34470
USA004 Tampa Florida 33613
USA010 Weston Florida 33331
USA028 Atlanta Georgia 30329
USA011 Sandy Springs Georgia 30328
USA003 Plainfield Indiana 46168
USA002 Baton Rouge Louisiana 70809-2725
USA017 Boston Massachusetts 02115
USA012 Detroit Michigan 48201
USA024 Fort Gratiot Michigan 48059
USA020 Minneapolis Minnesota 55455
USA015 St Louis Missouri 63104
USA013 Lebanon New Hampshire 03766
USA009 Cleveland Ohio 44106-1716
USA016 Springfield Ohio 45505
USA019 Hershey Pennsylvania 17033-2360
USA022 Philadelphia Pennsylvania 19104-5127
USA005 Dallas Texas 75230
USA023 Dallas Texas 75231-6077
USA008 Spokane Washington 99202

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 46 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT06685835, 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 28, 2026 · Synced Sep 2, 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 NCT06685835 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →