A Phase 3 interventional study of HFA MDI and HFO MDI in Asthma, sponsored by AstraZeneca. Completed at 4 sites in United States. Open to participants aged 18 Years to 45 Years. Per ClinicalTrials.gov, last updated 2026-02-06.
Sponsored by AstraZeneca · Phase 3, Interventional, and Treatment
A study to assess bronchospasm potentially induced by HFO MDI as compared with HFA MDI in participants with well controlled or partially controlled asthma
This is a phase 3b, multicentre, randomized, double-blind, single-dose crossover study comparing the safety and tolerability of HFO MDI with HFA MDI delivered in participants with well controlled or partially controlled asthma defined as an ACQ-5 score \< 1.5.Eligible participants are at least 18 years of age and no older than 45 years of age and are required to have asthma as defined by GINA guidelines (GINA 2022). Participants are required to be well controlled or partially controlled on their current treatment for asthma, including, low-dose ICS daily or low-dose ICS/formoterol as needed (not approved in the US), or SABA as needed, or low-dose ICS whenever SABA as needed is used. The primary objective is to assess the potential change in FEV1 induced by HFO MDI as compared with HFA MDI in participants with asthma.
This study will be conducted at approximately 5 sites in the US and will randomize approximately 52 adult participants to achieve 46 completers.
The study will be conducted for a maximal 37 days and will comprise:
Single dose study treatment will be administered via MDI device as 4 inhalations:
Age
Male and female participant must be 18 to 45 years of age inclusive, at the time of signing the informed consent form (ICF).
Type of Participant and Disease Characteristics
Participants who have a documented history of physician-diagnosed asthma
≥ 12 months prior to Visit 1, according to GINA guidelines (GINA 2022).
Demonstrate acceptable MDI administration technique.
Sex and Contraceptive/Barrier Requirements
Periodic abstinence (calendar, symptothermal, post-ovulation methods), withdrawal (coitus interruptus), spermicides only, and lactational amenorrhoea method are not acceptable methods of contraception. Female condom and male condom should not be used together. All women of childbearing potential must have a negative serum pregnancy test result at Visit 1.
Exclusion Criteria:
Medical Conditions
Known history of drug or alcohol abuse within 12 months of Visit 1.
Prior/Concomitant Therapy
Prior/Concurrent Clinical Study Experience 10 Participation in another clinical study with an investigational product administered within 30 days or 5 half-lives (whichever is longer). 11 Participants with a known hypersensitivity to HFO or HFA or any of the excipients of the product. 12 Previously randomized into a study with an HFO-containing MDI.
Diagnostic Assessments 13 Any clinically relevant abnormal findings in physical examination, clinical chemistry, hematology, urinalysis, vital signs, or electrocardiogram (ECG), which in the opinion of the investigator, may put the participant at risk because of his/her participation in the study. Note: Participants with ECG QT interval corrected for heart rate using Fridericia's formula (QTcF) > 480 msec will be excluded. Participants with high degree atrioventricular block II or III, or with sinus node dysfunction with clinically significant pauses who are not treated with pacemaker will also be excluded.
Other Exclusions 14 Involvement in the planning and/or conduct of the study (applies to both AstraZeneca staff and/or staff at the study site). 15 Judgment by the investigator that the participant should not participate in the study if the participant is unlikely to comply with study procedures, restrictions, and requirements.
16 Previous enrolment or randomisation in the present study. 17 For women only - currently pregnant (confirmed with positive pregnancy test), breast feeding, or planned pregnancy during the study or women of childbearing potential not using acceptable contraception measures. 18 Study investigators, sub-investigators, coordinators, and their employees or immediate family members.
Test arm, 4 inhalations per dose
Drug: HFO MDI
Reference arm, 4 inhalations per dose
Drug: HFA MDI
* Dose formulation: MDI * Unit dose strength(s): Reference (propellant only) * Dosage Level: 4 inhalations, single dose * Route of administration: Oral inhalation * Participants will receive treatment A in 1 or 2 possible sequences AB or BA
Also known as: Propellant in MDI
* Dose formulation: MDI * Unit dose strength(s): Experimental (propellant only) * Dosage Level: 4 inhalations, single dose * Route of administration: Oral inhalation * Participants will receive treatment A in 1 or 2 possible sequences AB or BA
Also known as: Propellant in MDI
Change From Baseline in Normalized Forced Expiratory Volume in 1 Second (FEV1) Area Under the Curve From 0 to 15 Minutes (AUC0-15 Min) Post-dose
The change from baseline (30 minutes pre-dose) in normalized FEV1 AUC0-15 min postdose induced by Treatment HFO was compared with Treatment HFA.
Time frame: 30 minutes prior to dosing and at 5, 15, and 30 minutes post-dose
Number of Participants With Bronchospasm Events
The potential of Treatment HFO to induce bronchospasm was compared with Treatment HFA. The number of participants with bronchospasm events post-dose (5 or 15 minutes post-dose) from baseline (30 minutes pre-dose) for each treatment is presented. An event of bronchospasm is defined as a reduction in FEV1 of \>15% from baseline (i.e. the FEV1 value obtained within 30 minutes prior to study intervention administration) at 5 or 15 minutes post-dose, with associated symptoms of wheezing, shortness of breath, or cough.
Time frame: 30 minutes prior to dosing and at 5 and 15 minutes post-dose
Safety and Tolerability Evaluated in Terms of Adverse Events (AEs)
The number of AEs, SAEs, and AESIs for Treatment HFO and Treatment HFA are presented.
Time frame: From screening (Day - 14) to the last dose (day 8) + 7 days
| Milestone | Sequence HFA-HFO | Sequence HFO-HFA |
|---|---|---|
| Started | 26 | 26 |
| Completed | 26 | 26 |
| Not completed | 0 | 0 |
The change from baseline (30 minutes pre-dose) in normalized FEV1 AUC0-15 min postdose induced by Treatment HFO was compared with Treatment HFA.
| Litres | Treatment HFO | Treatment HFA |
|---|---|---|
| Baseline FEV1 (30 minutes pre-dose) | 2.969 ± 0.6660 | 2.970 ± 0.6463 |
| Normalized FEV1 AUC0-15 min | 2.955 ± 0.6577 | 2.965 ± 0.6474 |
| Change from baseline in normalized FEV1 AUC0-15 min post-dose | -0.014 ± 0.0794 | -0.004 ± 0.0565 |
The potential of Treatment HFO to induce bronchospasm was compared with Treatment HFA. The number of participants with bronchospasm events post-dose (5 or 15 minutes post-dose) from baseline (30 minutes pre-dose) for each treatment is presented. An event of bronchospasm is defined as a reduction in FEV1 of \>15% from baseline (i.e. the FEV1 value obtained within 30 minutes prior to study intervention administration) at 5 or 15 minutes post-dose, with associated symptoms of wheezing, shortness of breath, or cough.
| Participants | Treatment HFO | Treatment HFA |
|---|---|---|
| Number of Participants With Bronchospasm Events | 0 (NC to NC) | 0 (NC to NC) |
The number of AEs, SAEs, and AESIs for Treatment HFO and Treatment HFA are presented.
| Events | Treatment HFO | Treatment HFA |
|---|---|---|
| Any AE | 2 | 4 |
| Serious AE (SAE) | 0 | 0 |
| Any SAE with outcome death | 0 | 0 |
| Any AE leading to discontinuation of investigational product | 0 | 0 |
| Any possibly related AE | 1 | 0 |
| Any possibly related SAE | 0 | 0 |
| Any AE of special interest | 0 | 0 |
Collected over The adverse events with start date on or after the date of treatment during treatment period 1 up to (and including) 7 days after the last dose date were included, up to 20 days.. Non-serious events are listed at a 0% frequency threshold.
| Group | Deaths | Serious | Other |
|---|---|---|---|
| Treatment HFO | 0/52 (0%) | 0/52 (0%) | 2/52 (3.8%) |
| Treatment HFA | 0/52 (0%) | 0/52 (0%) | 2/52 (3.8%) |
| Event | Treatment HFO | Treatment HFA |
|---|---|---|
| FatigueGeneral disorders | 0/52 | 1/52 |
| PyrexiaGeneral disorders | 1/52 | 0/52 |
| Urinary tract infectionInfections and infestations | 0/52 | 1/52 |
| DysgeusiaNervous system disorders | 1/52 | 0/52 |
| NephrolithiasisRenal and urinary disorders | 0/52 | 1/52 |
| Ovarian cystReproductive system and breast disorders | 0/52 | 1/52 |
| Age, Continuous(Years) | Sequence HFO-HFA | Sequence HFA-HFO | Total |
|---|---|---|---|
| Mean | 33.8 ± 9.78 | 30.9 ± 7.86 | 32.4 ± 8.90 |
| Age, Customized(Participants) | Sequence HFO-HFA | Sequence HFA-HFO | Total |
|---|---|---|---|
| 18-45 | 26 | 26 | 52 |
| Missing | 0 | 0 | 0 |
| Sex: Female, Male(Participants) | Sequence HFO-HFA | Sequence HFA-HFO | Total |
|---|---|---|---|
| Female | 17 | 19 | 36 |
| Male | 9 | 7 | 16 |
| Ethnicity (NIH/OMB)(Participants) | Sequence HFO-HFA | Sequence HFA-HFO | Total |
|---|---|---|---|
| Hispanic or Latino | 8 | 7 | 15 |
| Not Hispanic or Latino | 18 | 19 | 37 |
| Unknown or Not Reported | 0 | 0 | 0 |
| Race (NIH/OMB)(Participants) | Sequence HFO-HFA | Sequence HFA-HFO | Total |
|---|---|---|---|
| American Indian or Alaska Native | 1 | 0 | 1 |
| Asian | 0 | 1 | 1 |
| Native Hawaiian or Other Pacific Islander | 0 | 0 | 0 |
| Black or African American | 3 | 4 | 7 |
| White | 22 | 21 | 43 |
| More than one race | 0 | 0 | 0 |
| Unknown or Not Reported | 0 | 0 | 0 |
| Country(Participants) | Sequence HFO-HFA | Sequence HFA-HFO | Total |
|---|---|---|---|
| USA | 26 | 26 | 52 |
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