The Safety, Feasibility, and Repeatability of Inhaled ATP Cough Challenges

NCT ID: NCT07085975

Last Updated: 2025-08-29

Basic Information

• Recruitment Status: RECRUITING
• Clinical Phase: PHASE1
• Total Enrollment: 33 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2025-08-05
• Study Completion Date: 2026-10-01

Brief Summary

The inhalation of adenosine 5'-triphosphate (ATP) to evoke cough (ATP cough challenge) is becoming increasingly used as a tool to measure cough hypersensitivity in patients with chronic cough. However, the safety, feasibility, and repeatability of this procedure is not widely known. In this study, we will perform ATP cough challenges in healthy individuals and in patients with mild asthma and chronic cough to better understand the safety, feasibility, and repeatability of these challenges. Such information will guide the future conduct of ATP cough challenges to measure cough hypersensitivity and identify patients who may better respond to ATP-blocking therapies.

Conditions

Chronic Cough (CC); Asthma

Study Design

• Allocation Method: NA
• Intervention Model: SINGLE_GROUP
• Primary Study Purpose: DIAGNOSTIC
• Blinding Strategy: NONE

Study Groups

Adenosine 5'triphosphate

Group Type: EXPERIMENTAL

Adenosine 5'-triphosphate

Intervention Type: DRUG

Participants will inhale increasing doubling concentrations of adenosine 5'-triphosphate dissolved in 0.9% saline through the Aerogen Solo vibrating mesh nebulizer.

Interventions

Adenosine 5'-triphosphate

Participants will inhale increasing doubling concentrations of adenosine 5'-triphosphate dissolved in 0.9% saline through the Aerogen Solo vibrating mesh nebulizer.

Intervention Type: DRUG

Eligibility Criteria

Inclusion Criteria

Eligible participants in Phase 1 will include healthy adults (≥18 years old) with:

1. Normal spirometry; and

2. No current or past medical history of chronic cough or other respiratory diseases.

Eligible participants will include adults (≥18 years old) with:

1. RCC/UCC for >1 year, demonstrated by a normal chest radiograph and no airflow obstruction (FEV1/FVC>0.7/LLN) with either:

1. Insufficient improvement in cough despite treatment targeting any underlying condition(s) contributing to the cough (RCC); or

2. Cough for which an underlying cause has not been determined despite thorough investigation (UCC).

2. Mild steroid-naïve asthma who demonstrate evidence of a positive screening methacholine (PC20<16 mg/mL); symptoms of cough, shortness of breath, chest tightness, and wheeze, that, in the opinion of the qualified investigator, are well-controlled; and those have not used inhaled or oral corticosteroids for the past month.

Exclusion Criteria

We will exclude healthy individuals meeting the following:

(1) Are a current or former smoker with a >5 pack-year history and abstinence ≤6 months;

1. Unable to perform acceptable and reproducible spirometry;

2. Have unresolved symptoms of upper respiratory tract infection within 6 weeks prior to the first study visit;

3. Have had a lower respiratory tract infection or pneumonia within 6 weeks prior to the first study visit;

4. Presence of other primary pulmonary disorders, including pulmonary embolism, pulmonary hypertension, lung cancer, cystic fibrosis, radiologically-proven emphysema, severe bronchiectasis, or severe interstitial lung disease; or

5. History of psychiatric illness, drug, or alcohol abuse that could interfere with participation in the study.

6. History of clinically-significant cardiovascular disease, including coronary artery disease, aortic aneurysm, or stroke in the last 3 months;

7. Those with serious medical conditions or those who are not on stable medication(s) for their condition(s);

8. Those with immune system disorders, severe allergy, or on allergy-specific immunotherapy;

9. Any other condition, that, in the opinion of the qualified investigator, may adversely affect the participant's ability to complete the study or its measures or pose significant risk to the participant;

10. Pregnant or breastfeeding;

11. Women of child-bearing potential who:

1. Do not agree to use a medically approved method of birth control for the duration of the study. All hormonal birth control must have been in use for a minimum of 3 months. Acceptable methods of birth control include oral contraceptives, hormone birth control patch, vaginal contraceptive ring, injectable contraceptives, or hormone implant, double-barrier method, intrauterine devices, non-heterosexual lifestyle or agrees to use contraception if planning on changing to heterosexual partner(s), vasectomy of partner at least 6 months prior to screening. Females who are not of child-bearing potential will be defined as females who have undergone a sterilization procedure (e.g., hysterectomy, bilateral oophorectomy, bilateral tubal ligation, complete endometrial ablation) or have been post-menopausal for at least 1 year prior to screening.

Phase 2: Patients with RCC/UCC and mild-steroid naïve asthma

For the RCC/UCC cohort:

(1) Current smoker or ex-smoker with ≥20 pack-year history and abstinence ≤6 months;

For the mild steroid-naïve asthma cohort:

1. Current smoker or ex-smoker with ≥20 pack-year history and abstinence ≤6 months;

2. History or exacerbation or uncontrolled symptoms within the last month prior to the first study visit; and

3. Use of inhaled or oral corticosteroids within the last month prior to the first study visit.

We will exclude participants meeting any of the following criteria from the study:

1. Unable to perform acceptable and reproducible spirometry;

2. Unresolved symptoms of upper respiratory tract infection within 6 weeks prior to the first study visit;

3. Lower respiratory tract infection or pneumonia within 6 weeks prior to the first study visit;

4. Presence of other primary pulmonary disorders, including pulmonary embolism, pulmonary hypertension, lung cancer, cystic fibrosis, radiologically-proven emphysema, severe bronchiectasis, or severe interstitial lung disease;

5. History of psychiatric illness, drug, or alcohol abuse that could interfere with participation in the study;

6. History of clinically-significant cardiovascular disease, including coronary artery disease, aortic aneurysm, or stroke in the last 3 months;

7. Those with serious medical conditions or those who are not on stable medication(s) for their condition(s);

8. Those with immune system disorders, severe allergy, or on allergy-specific immunotherapy;

9. Any other condition, that, in the opinion of the qualified investigator, may adversely affect the participant's ability to complete the study or its measures or pose significant risk to the participant;

10. Pregnant or breastfeeding;

11. Female participants of child-bearing potential who:

1. Do not agree to use a medically approved method of birth control for the duration of the study;

2. Have not been using hormonal birth control for a minimum of 3 months prior to screening.

• Minimum Eligible Age: 18 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: Yes

Sponsors

McMaster University

OTHER

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Locations

Respiratory Research Lab

Hamilton, Ontario, Canada

Site Status: RECRUITING

Countries

Canada

Central Contacts

Imran Satia, MD PhD

Role: CONTACT

satiai@mcmaster.ca

905-525-2100 ext. 76228

Facility Contacts

Imran Satia, MD PhD

Role: primary

satiai@mcmaster.ca

905-521-2100 ext. 76645

Other Identifiers

ATP-17839

Identifier Type: -

Identifier Source: org_study_id