New pill shows promise for stubborn cough that Won't quit
NCT ID NCT05733533
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study tested an experimental drug called HRS-2261 in 97 adults with refractory chronic cough—a persistent cough that doesn't respond to usual treatments. Participants took the drug or a placebo for 4 weeks to see if it reduced cough severity and improved quality of life. The goal is to find a safe, effective option for people who have suffered from chronic cough for over a year.
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Study facts
What this study's own registry entry says, in plain language.
- Phase
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Phase 2
Tests whether the treatment actually works, and watches for side effects, in a larger group.
- Participants
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97 people
The number who actually took part.
- Started
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Mar 2023
- Finished
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Mar 2024
- Lead sponsor
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A company
The lead sponsor is a pharmaceutical, biotech, or medical-device company.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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18 years and older
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: 1. ≥18 years of age; 2. Diagnosed with refractory chronic cough or chronic cough of unknown cause, with a course of disease lasting more than 1 year; 3. Within 5 years prior to screening and after the onset of chronic cough, chest imaging did not reveal any significant abnormalities that the investigators considered to cause chronic cough or any other clinically significant lung disease; 4. VAS scores of cough severity in screening period and baseline period ≥ 40 mm; 5. Subjects receiving medication for pre-existing underlying conditions prior to the screening period should stabilize the corresponding dose for at least 8 weeks prior to screening; 6. Take effective contraceptive measures; 7. Voluntarily sign informed consent to participate in this study; 8. Willing and able to comply with all protocol requirements, including demonstrating the ability to comply with study procedures prior to random assignment. Exclusion Criteria: 1. Patients diagnosed with chronic obstructive pulmonary disease (COPD), bronchiectasis, idiopathic pulmonary fibrosis (IPF), and endobronchial tuberculosis; 2. Patients with a history of chronic bronchitis; 3. Patients with a history of upper or lower respiratory tract infection, or acute exacerbation of respiratory disease, or significant changes in chest imaging within 4 weeks prior to baseline period; 4. Current smokers, smokers who have quit smoking (within 6 months), or former smokers who consume more than 20 packs of cigarettes per year; 5. Those with abnormal taste within 3 months prior to previous diagnosis or screening; 6. Malignant disease within 5 years or less before signing the informed consent, except for basal cell or squamous cell skin cancer or cervical cancer in situ after appropriate treatment; 7. Currently taking or having taken an angiotensin-converting enzyme inhibitor in the 3 months prior to screening; 8. Those who are currently taking or have used any antitussive medication within the week prior to screening; 9. Patients who had used oral steroids or antiallergy drugs within 1 week prior to screening; 10. Screening or baseline 1 second rate \< 60%; 11. Poorly controlled hypertension; 12. Alanine aminotransferase or aspartate aminotransferase more than 2 times the upper limit of normal in screening period or baseline period; 13. Estimated glomerular filtration rate (eGFR) \< 30mL/min/1.73m2 or eGFR≥30mL/min/1.73m2 and \<50mL/min/1.73m2 with unstable renal function during screening; 14. Use of systemic immunosuppressants or immunomodulators, or biologics or Th2 cytokine inhibitors within 12 weeks prior to randomization or within 5 half-lives of the drug; 15. A recent history of drug or alcohol abuse or dependence (within the past 1 year); 16. Participants enrolled in clinical trials of any drug or medical device within 3 months prior to screening, or within 5 half-lives of test drugs before screening, whichever is longer; 17. Any past or present circumstances, determined by the investigator or sponsor, make the subject unfit for admission to the study.
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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The First Affiliated Hospital of Guangzhou Medical University
Guangzhou, Guangdong, 510120, China
More trials for these conditions
Other studies related to the condition(s) this trial covers.
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