Could a simple magnesium spray quiet a chronic cough?
NCT ID NCT07690059
First seen Jul 08, 2026 · Last updated Sep 09, 2026 · Updated 3 times
Summary
This study tests whether a magnesium salt oral spray, called SC0032, can safely reduce coughing in adults with refractory or unexplained chronic cough—a cough that persists despite treatment or has no clear cause. Participants are randomly assigned to receive either the magnesium spray or a placebo (sodium chloride spray) for about three weeks. The main goal is to measure changes in 24-hour cough frequency using a special monitor.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- magnesium chloride oral spray
- What this could lead to
- If effective, this spray could offer a new, drug-free option to reduce coughing in people with chronic cough that doesn't respond to other treatments.
- What could go wrong
- This is a small, early-phase pilot study. The spray may not reduce cough more than placebo, and individual results may vary. Long-term safety and effectiveness are not yet known.
This is an AI summary of the original study and may miss details. Read our disclaimer.
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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About 60 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Jul 2026
- Expected to finish
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Apr 2027
An estimate. End dates often move.
- 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 to 80 years
- 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. Males and females between 18 and 80 years. 2. Capable of giving signed informed consent. 3. Diagnosed with RCC (including unexplained chronic cough) for at least 6 months. 4. At least 8 coughs per hour, 24-hour cough frequency during the 14-day Run-In Period. 5. Score ≥ 40 mm on cough severity VAS at Screening. 6. Normal FEV1/FVC ratio of greater than 70% at Screening 7. A negative test for COVID-19. 8. Women of child-bearing potential and men must agree to use a highly effective contraception method during the study and for at least 14 days after the last dose. 9. Willing to carry study-related equipment as required for the study (e.g. cough monitor, phone). Exclusion Criteria: 1. Current smoker/vaper (all forms of smoking and inhaled substances, including cannabis/tobacco smoke and nicotine vapours) or individuals who have given up smoking within the past 6 months, or those with \>20 pack-year smoking history. 2. Diagnosis of Chronic Obstructive Pulmonary Disease (COPD), bronchiectasis, idiopathic pulmonary fibrosis, uncontrolled asthma or other serious pulmonary disease. 3. Respiratory tract infection within 4 weeks before screening. 4. History of malignancy in the last 5 years, unless it is a non-serious skin cancer. 5. History of moderate or severe alcohol or drug use disorder within the last 3 years. 6. Opioid use with in the 7 days prior to screening. 7. History of a positive serologic test for hepatitis B virus surface antigen, or hepatitis C virus. 8. Previous participation in a clinical trial in the last 30 days or 6-half half-lives of test drug activity. 9. Current participation in or completion of speech language therapy intervention therapy for chronic cough within 8 weeks prior to screening. 10. Use of Prohibited medications within 4 weeks prior to screening and at any time during the study: anti-tussive therapy, systemic corticosteroids, ACE inhibitors, opioids. 11. Gabapentin and pregabalin are prohibited unless they are being administered for treatment of a condition other than RCC and have been on a stable dose of that medication for at least 6 weeks prior to screening and plan to remain on that dose for the duration of the study. 12. Tricyclic antidepressants are prohibited unless they are being administered for treatment of a condition other than RCC and have been on a stable dose of that medication for at least 12 weeks prior to screening and plan to remain on that dose for the duration of the study. 13. Beta blockers are prohibited unless they are on a stable dose for at least 6 weeks prior to screening. 14. Use of dietary supplements containing magnesium for the duration of the study. 15. History of myocardial infarction or other cardiac disorders as follows: * History of any of the following within 6 months prior to screening, myocardial infarction, stroke or transient ischemic attack, coronary revascularization (PCI or CABG), or heart failure. * History of clinically significant arrhythmias, poorly controlled hypertension. * Any condition that, in the opinion of the investigator, places the participant at high risk for an acute cardiovascular event including but not limited to: angina symptomatic peripheral arterial disease, severe valvular heart disease, planned cardiovascular intervention or surgery during the study period, baseline QTc interval \>450 ms (men) or \>470 ms (women), or any clinically significant ECG abnormality as determined by the Investigator. 16. History of any clinically significant or psychiatric condition that, in the eyes of the Investigator or designee, would not be suitable for this study. Or if, in the eyes of the Investigator or designee may prove non-compliant to study procedures. 17. Spouses or other family members with a chronic cough in the household. 18. Living and working in an excessively loud workplace (e.g. building site).
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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.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
3 sites. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
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Kings College Hospital
RECRUITINGLondon, SE5 9RS, United Kingdom
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Royal Brompton Hospital
RECRUITINGLondon, SW3 6NP, United Kingdom
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The Wellcome Trust-Wolfson Northern Ireland Clinical Research Facility U Floor, Belfast City Hospital
NOT_YET_RECRUITINGBelfast, BT9 7AB, United Kingdom