Overview

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.

Principal investigator

Alejandro Comellas Freymond
Internal Medicine

Eligibility criteria

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
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For Referring Providers

Do you have a patient you think would be a good candidate for this trial? Learn more about enrolling your patient.

Contact the study coordinator

Maria Aguilar Pescozo
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