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Completed Phase 2 Interventional

A Study of the Efficacy and Safety of Brensocatib in Participants With Chronic Rhinosinusitis Without Nasal Polyps (CRSsNP)

ClinicalTrials.gov ID: NCT06013241

Public ClinicalTrials.gov record NCT06013241. 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 Nov 2, 2026, 11:50 AM EST

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 Participants With Chronic Rhinosinusitis Without Nasal Polyps - The BiRCh Study

Brief summary

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

The primary purpose of the study is to evaluate the efficacy of brensocatib at 10 and 40 milligrams (mg) once daily (QD) compared with placebo in improving clinical symptoms of CRSsNP.

Study identification

NCT ID
NCT06013241
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Insmed Incorporated
Industry
Enrollment
288 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years to 75 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
Oct 30, 2023 (Actual)
Primary completion
Sep 30, 2025 (Actual)
Completion
Oct 30, 2025 (Actual)
Last update posted
Sep 30, 2026

2023 – 2025

United States locations

U.S. sites
27
U.S. states
14
U.S. cities
24
Facility City State ZIP Site status
USA034 Tucson Arizona 85704 —
USA002 Roseville California 95661 —
USA006 Upland California 91786 —
USA016 Boca Raton Florida 33487 —
USA019 Hollywood Florida 33024 —
USA001 Miami Florida 33135 —
USA009 Tampa Florida 33613 —
USA031 Chicago Illinois 60611 —
USA021 Chicago Illinois 60612 —
USA003 New Albany Indiana 47150 —
USA035 Mandeville Louisiana 70471 —
USA026 Baltimore Maryland 21287 —
USA011 Columbia Missouri 65212 —
USA024 St Louis Missouri 63141 —
USA033 New York New York 10016 —
USA028 Tulsa Oklahoma 74132 —
USA004 Tulsa Oklahoma 74136 —
USA015 Hershey Pennsylvania 17033 —
USA023 Charleston South Carolina 29425 —
USA022 North Charleston South Carolina 29406 —
USA025 Dallas Texas 75231 —
USA037 Fredericksburg Texas 78624 —
USA029 Houston Texas 77022 —
USA018 Houston Texas 77030 —
USA030 San Antonio Texas 78258 —
USA038 Tomball Texas 77375 —
USA005 Norfolk Virginia 23507 —

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 73 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT06013241, 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 Sep 30, 2026 · Synced Nov 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 public registry record, listed eligibility criteria, and available contact information for NCT06013241 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →