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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT05599191
Other study ID # 221850
Secondary ID BUS-P3-01
Status Recruiting
Phase Phase 3
First received
Last updated
Start date October 25, 2022
Est. completion date March 2026

Study information

Verified date February 2024
Source Bellus Health Inc. - a GSK company
Contact US GSK Clinical Trials call Center
Phone 877-379-3718
Email GSKClinicalSupportHD@gsk.com
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This is a randomized, double-blind, placebo-controlled, parallel-arm, Phase 3 study of BLU-5937 in participants with Refractory Chronic Cough (RCC).


Description:

The primary efficacy objective is to assess the effect of BLU-5937 on 24-hour cough frequency in adults with refractory chronic cough (including unexplained chronic cough) at 12 weeks.


Recruitment information / eligibility

Status Recruiting
Enrollment 825
Est. completion date March 2026
Est. primary completion date September 2025
Accepts healthy volunteers No
Gender All
Age group 18 Years to 80 Years
Eligibility Inclusion Criteria: - Capable of giving signed informed consent - Refractory chronic cough (including unexplained chronic cough) for at least one year - Women of child-bearing potential must use a highly effective contraception method during the study and for at least 14 days after the last dose Exclusion Criteria: - Current smoker/vaper (all forms of smoking and inhaled substances, including , cannabis/tobacco smoke and nicotine vapors) or individuals who have given up smoking within the past 6 months, or those with >20 pack-year smoking history - Diagnosis of Chronic Obstructive Pulmonary Disease (COPD), bronchiectasis, idiopathic pulmonary fibrosis or uncontrolled asthma - Respiratory tract infection within 4 weeks before screening - Laboratory confirmed Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2) infection at screening - History of malignancy in the last 5 years - History of alcohol or drug abuse within the last 3 years - Has a positive serologic test for human immunodeficiency virus (HIV), hepatitis B virus surface antigen, or hepatitis C virus. - Previous participation in a BLU-5937 trial

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
BLU-5937
Oral administration of BLU-5937 Tablets
Placebo
Oral administration of matching placebo for BLU-5937 Tablets

Locations

Country Name City State
Argentina Expertia S.A- Mautalen Salud e Investigación Ciudad Autonoma Buenos Aires Buenos Aires
Argentina Hospital Italiano de Buenos Aires Ciudad Autonoma Buenos Aires
Argentina CINME - Centro De Investigaciones Metabolicas Ciudad Autonoma de Buenos Aire Buenos Aires
Argentina APRILLUS Asistencia e Investigacion Ciudad Autonoma de Buenos Aires Ciudad Autonoma Buenos Aires
Argentina Instituto Medico DAMIC Cordoba
Argentina Centro de Investigaciones Medicas Mar del Plata Mar del Plata Buenos Aires
Argentina Fundacion Scherbovsky Mendoza
Argentina Insares S.A. Mendoza
Argentina Instituto de Especialidades de la Salud Rosario Rosario Santa Fe
Argentina Instituto Medico de la Fundacion Estudios Clinicos Rosario Santa Fe
Argentina Instituto Medico Fundación Grupo Colaborativo Rosario Investigación y Prevención Medica Rosario Santa Fe
Argentina Instituto del Buen Aire Santa Fe
Argentina CEMER - Centro Medico de Enfermedades Respiratorias Vicente López Buenos Aires
Belgium Cliniques Universitaires Saint-Luc Bruxelles
Belgium Universitair Ziekenhuis Gent Gent
Belgium C. H. R. de la Citadelle Liège
Belgium AZ Sint-Maarten Mechelen
Canada Dynamic Drug Advancement Ajax Ontario
Canada Burlington Lung Clinic Burlington Ontario
Canada Peak Research Group Calgary Alberta
Canada University of Calgary - Health Sciences Centre Calgary Alberta
Canada CISSS de la Monteregie-Centre Greenfield Park Quebec
Canada Hamilton Medical Research Group Hamilton Ontario
Canada McMaster University Health Sciences Center Hamilton Ontario
Canada Kelowna Respirology and Asthma Research Kelowna British Columbia
Canada Montreal Chest Institute Montréal Quebec
Canada Recherche GCP Research Montréal
Canada Clinique Specialisee en Allergie de la Capitale Québec Quebec
Canada DIEX Recherche Quebec Inc. Québec Quebec
Canada Institut Universitaire de Cardiologie et de Pneumologie de Quebec Québec Quebec
Canada Clinique de pneumologie et du sommeil de Lanaudière Saint-Charles-Borromée Quebec
Canada Inspiration Research Limited Toronto Ontario
Canada CIC Mauricie Inc. Trois-Rivières Quebec
Canada DIEX Recherche Victoriaville Inc. Victoriaville Quebec
Canada Dr. Syed Anees Medicine Professional Corporation Windsor Ontario
Colombia Fundación Cardiovascular de Colombia - Instituto del Corazón Floridablanca Floridablanca
Colombia Asociacion IPS Medicos Internistas de Caldas Manizales
Colombia Clinica SOMER Medellín
Colombia Fundacion Centro de Investigacion Clinica CIC Medellín
Colombia Hospital Pablo Tobón Uribe Medellín
France CHU de Dijon - Hôpital François Mitterand Dijon cedex Côte-d'Or
France Hopital Albert Calmette CHU Lille Lille
France Hopital Européen de Marseille Marseille Bouches-du-Rhône
France Hôpital Nord - CHU Marseille Marseille Bouches-du-Rhône
France Hopital Arnaud de Villeneuve Montpellier cedex 5 Herault
France Hôpital Cochin Paris
France CHU de Strasbourg - Nouvel Hôpital Civil Strasbourg Bas Rhin
France Hopital Larrey Toulouse Haute Garonne
Hungary DRC Gyogyszervizsgalo Kozpont Kft. Balatonfüred
Hungary Clinexpert Kft. Budapest
Hungary Omnimodus Elixir Kft. Csorna
Hungary Erzsebet Gondozohaz Kft. Gödöllo
Hungary Szalay Janos Rendelointezet Hajdunanas
Hungary Da Vinci Maganklinika Pécs
Hungary Puspokladanyi Egeszsegugyi Szolgaltato Nonprofit Kft. Püspökladány
India Shetty Hospital Bengaluru Karnataka
India Institute of Medical Sciences and SUM Hospital Bhubaneswar Orissa
India Indraprastha Apollo Hospitals Delhi
India Asthma Bhavan Jaipur Rajasthan
India Calcutta Medical Research Institute Kolkata West Bengal
India Siddhi Hospital Nashik Maharashtra
India Suyog Multispeciality Hospital Nashik Maharashtra
India ACE Hospital and Research Centre Pune Masharashtra
India Pandit Bhagwat Dayal Sharma Post Graduate Institute of Medical Sciences Rohtak Haryana
India Bhaktivedanta Hospital and Research Institute Thane Maharashtra
India Aashirwad Hospital Ulhasnagar Maharashtra
Israel Hillel Yaffe Medical Center Hadera
Israel The Lady Davis Carmel Medical Center Haifa
Israel Hadassah University Hospital - Ein Kerem Jerusalem
Israel Rabin Medical Center-Beilinson Campus Petach Tikva
Israel Sheba Medical Center Ramat Gan
Israel Tel Aviv Sourasky Medical Center Tel Aviv
Netherlands Noordwest Ziekenhuisgroep Alkmaar
Netherlands Rijnstate Arnhem
Netherlands Amphia Ziekenhuis, Molengracht Breda
Netherlands Bernhoven Uden Uden
Netherlands Gelre Ziekenhuizen, Zutphen Zutphen
Netherlands Isala Klinieken, Weezenlanden Zwolle
Poland Prywatny Gabinet Internistyczno-Alergologiczny Bialystok
Poland Centrum Medyczne Pratia Bydgoszcz Bydgoszcz
Poland Uniwersytecki Szpital Kliniczny nr 1 im. N. Barlickiego w Lodzi Lódz
Poland Uniwersytecki Szpital Kliniczny nr 1 im. Norberta Barlickiego Lódz
Poland Ostrowieckie Centrum Medyczne spólka cywilna Anna Olech-Cudzik, Krzysztof Cudzik Ostrowiec Swietokrzyski
Poland Center of Innovative Therapies Piaseczno
Poland Prywatny Gabinet Lekarski Rzeszów
Poland Alergo-Med Specjalistyczna Przychodnia Lekarska Sp. Z .O.O. Tarnów
Poland Centrum Medyczne Lucyna Andrzej Dymek s.c. Zawadzkie
South Africa Iatros International Bloemfontein Free State
South Africa Dr NK Gounden Medi-Centre Durban KwaZulu-Natal
South Africa TASK Eden George Western Cape
South Africa Smith, C - Morningside Hospital Johannesburg Gauteng
South Africa Worthwhile Clinical Trials Johannesburg Gauteng
South Africa Botho ke Bontle Health Services Pretoria Gauteng
South Africa Global Clinical Trials Pretoria Gauteng
South Africa Dr JM Engelbrecht Trial Site Somerset West Western Cape
Spain Accellacare España SL Alcobendas Madrid
Spain Hospital Clinic de Barcelona Barcelona
Spain Hospital de la Santa Creu i Sant Pau Barcelona
Spain Hospital General Universitario Gregorio Marañon Madrid
Spain Hospital Universitario Clinico San Carlos Madrid
Spain Hospital Universitario de La Princesa Madrid
Spain Hospital Clinico Universitario Virgen de la Victoria Málaga
Spain Hospital Quironsalud Malaga Málaga
Spain Hospital Universitario Quironsalud Madrid Pozuelo De Alarcón Madrid
Spain Complejo Hospitalario Universitario de Santiago Santiago De Compostela La Coruña
Turkey Sureyyapasa Pulmonary Diseases and Cardiothoracic Surgery Education and Research Hospital Istanbul
Turkey Yedikule Pulmonary Dis. and Surgery Edu. and Res. Hosp. Istanbul
Turkey Ege University Medical Faculty Izmir
Turkey Kocaeli Universitesi - Kocaeli Universitesi Tip Fakultesi Izmit
Turkey Mersin University Medical Faculty Mersin
Turkey TC SBU Izmir Dr Suat Seren Gogus Hastaliklari ve Cerrahisi Egitim ve Arastirma Yenisehir
United Kingdom Belfast City Hospital Belfast
United Kingdom West Walk Surgery Bristol
United Kingdom Lakeside Healthcare Corby Northamptonshire
United Kingdom Holderness Health Hull East Riding Of Yorkshire
United Kingdom Royal Brompton Hospital London Greater London
United Kingdom Accellacare North London Northwood Middlesex
United Kingdom Norfolk and Norwich University Hospital Norwich Norfolk
United Kingdom Accellacare South London Orpington Kent
United Kingdom Accellacare Yorkshire Shipley Bedfordshire
United Kingdom Wythenshawe Hospital Wythenshawe Greater Manchester
United States McFarland Clinic P.C. Ames Iowa
United States Michigan Medicine Investigational Drug Services Ann Arbor Michigan
United States Care Access Research Aurora Colorado
United States The Asthma and Allergy Center Bellevue Nebraska
United States Bellingham Asthma, Allergy & Immunology Clinic Bellingham Washington
United States Accellacare Bristol Bristol Tennessee
United States Montefiore Medical Center (MMC) Bronx New York
United States Lowcountry Lung and Critical Care, P.A. Charleston South Carolina
United States American Health Research, Inc. Charlotte North Carolina
United States Innovative Research of West Florida, Inc. Clearwater Florida
United States The Curators of the University of Missouri on behalf of University of Missouri Health Care Columbia Missouri
United States Remington-Davis, Inc. Columbus Ohio
United States Avant Research Associates, LLC Crowley Louisiana
United States Pharmaceutical Research & Consulting, Inc. Dallas Texas
United States Omega Research Consultants DeBary Florida
United States PMG Research of DuPage Medical Group Downers Grove Illinois
United States Clinical Research Associates of Central PA, LLC DuBois Pennsylvania
United States Warren W. Pleskow, MD, 1071572 Encinitas California
United States North Florida Foundation for Research and Education, Inc. Gainesville Florida
United States The Community Research of South Florida Hialeah Florida
United States Clinical Trial Network LLC Houston Texas
United States University of Texas Health Science Center at Houston Houston Texas
United States University of Iowa Hospitals & Clinics Iowa City Iowa
United States Jasper Summit Research, LLC Jasper Alabama
United States University of Kansas Medical Center Research Institute, Inc. Kansas City Kansas
United States PMG Research of Knoxville Knoxville Tennessee
United States Sher Allergy Largo Florida
United States Gwinnett Pulmonary Group P.C. Lawrenceville Georgia
United States Research Solutions of Arizona, PC Litchfield Park Arizona
United States Main Street Physician's Care - Waterway Little River South Carolina
United States Little Rock Allergy & Asthma, P.A. Clinical Research Center Little Rock Arkansas
United States Metroplex Pulmonary and Sleep Center McKinney Texas
United States Velocity Clinical Research Medford Oregon
United States Coral Research Clinic corp Miami Florida
United States Cordova Research Institute, LLC Miami Florida
United States Life Spring Research Foundation Miami Florida
United States Well Pharma Medical Research Corporation Miami Florida
United States Allergy & Asthma Research of Southern California Mission Viejo California
United States Montana Medical Research, Inc. Missoula Montana
United States PMG Research of Charleston, LLC Mount Pleasant South Carolina
United States Eastern Virginia Medical School Norfolk Virginia
United States Sneeze, Wheeze and Itch Associates, LLC Normal Illinois
United States Infinity Medical Research Inc North Dartmouth Massachusetts
United States University of Oklahoma Health Sciences Center Oklahoma City Oklahoma
United States Center for Clinical Trials, LLC Paramount California
United States Temple Lung Center Philadelphia Pennsylvania
United States Allergy Associates Research Center Portland Oregon
United States PMG Research of Raleigh Raleigh North Carolina
United States Clinical Research of Rock Hill Rock Hill South Carolina
United States PMG Research of Rocky Mount, LLC Rocky Mount North Carolina
United States PMG Research of Salisbury, LLC Salisbury North Carolina
United States University of Utah Hospitals & Clinics Salt Lake City Utah
United States Diagnostics Research Group, LLC San Antonio Texas
United States Allergy Associates Medical Group, Inc. San Diego California
United States Medical Research of Arizona Scottsdale Arizona
United States Cotton O'Neil Clinical Research Center Topeka Kansas
United States Vital Prospects Clinical Research Institute, P.C. Tulsa Oklahoma
United States Allergy Asthma Research Institute Waco Texas
United States AAPRI Clinical Research Institute Warwick Rhode Island
United States University of Kansas Medical Center Research Institute, Inc. Wichita Kansas
United States TPMG Clinical Research Williamsburg Williamsburg Virginia
United States Southeastern Research Center LLC Winston-Salem North Carolina

Sponsors (1)

Lead Sponsor Collaborator
Bellus Health Inc. - a GSK company

Countries where clinical trial is conducted

United States,  Argentina,  Belgium,  Canada,  Colombia,  France,  Hungary,  India,  Israel,  Netherlands,  Poland,  South Africa,  Spain,  Turkey,  United Kingdom, 

Outcome

Type Measure Description Time frame Safety issue
Primary 24-Hour Cough Frequency Assessed using an ambulatory cough monitor Week 12
Secondary Change from Baseline in Cough Severity Visual Analogue Scale at Week 12 Assessed by Cough Severity Visual Analogue Scale [VAS] by the participant on a 100 mm visual analog scale where higher scores indicate greater severity. Baseline, Week 12
Secondary Percentage of Participants With = 30mm Reduction, = 20mm Reduction From Baseline in Cough Severity Visual Analog Scale (VAS) at Week 12 Assessed by Cough Severity Visual Analogue Scale [VAS] by the participant on a 100 mm visual analog scale where higher scores indicate greater severity. Baseline, Week 12
Secondary Percentage of Participants With =30%, =50%, and =70% Reduction From Baseline in 24-Hour Cough Frequency at Week 12 Assessed using an ambulatory cough monitor Baseline, Week 12
Secondary Change from Baseline in the Leicester Cough Questionnaire (LCQ) Total Score at Week 12 The LCQ is a patient-reported quality of life (QOL) measure of chronic cough. The questionnaire consists of 19 items to which the patient responds on a 7-point Likert response scale (from 1 to 7). Each item assesses symptoms during cough and the impact of cough on 3 domains: physical, psychological, and social. Domain scores range from 1-7, and the total score ranges from 3 - 21; a higher score indicates a better quality of life. Baseline, Week 12
Secondary Percentage of Participants With a =1.3-point Increase From Baseline in Leicester Cough Questionnaire (LCQ) Total Score at Week 12 The LCQ is a patient-reported quality of life (QOL) measure of chronic cough. The questionnaire consists of 19 items to which the patient responds on a 7-point Likert response scale (from 1 to 7). Each item assesses symptoms during cough and the impact of cough on 3 domains: physical, psychological, and social. Domain scores range from 1-7, and the total score ranges from 3 - 21; a higher score indicates a better quality of life. Baseline, Week 12
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