A Study Evaluating the Effect of Inhaled PT007(AS MDI) Versus Placebo MDI and Ventolin Evohaler on Lung Function in Adult Participants With Asthma

Completed · Phase 2 · Has a placebo group

Conditions studied: Asthma

In brief

Phase II study, to investigate the therapeutic efficacy and safety of inhaled PT007 (referred to as AS MDI) compared with placebo MDI and open-label Ventolin Evohaler in male and female participants aged 18 to 65 years (inclusive) with asthma. This study consists of a screening/run-in period, a treatment period, and a follow-up phone call.

Key facts

Study ID

NCT06644924

Run by

AstraZeneca

People needed

118

Starts

2025-02-10

Expected to finish

2025-06-04

Last updated by the study team

2025-09-03

Who can join

Age: 18 and older, up to 65. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Age
• Participant must be aged 18 to 65 years (inclusive), at the time of signing the informed consent.
• Type of Participant and Disease Characteristics
• Participants should have a documented history of physician-diagnosed asthma ≥ 6 months prior to Visit 1.
• Must be receiving one of the following required inhaled asthma therapies listed below for at least the last 30 days:
• Only SABA, which is used as needed for rescue.
• Low to medium doses of ICS (alone or in combination with LABA), used regularly as maintenance asthma therapy.
• Pre-BD FEV1 of ≥ 40% of the PN value at Visit 1, after withholding SABA for ≥ 6 hours (and Visit 1a and/or Visit 1b, if applicable).
• Confirmed FEV1 reversibility to 4 actuations of Ventolin HFA, defined as a post-Ventolin HFA increase in FEV1 at 30 minutes of ≥ 12% and ≥ 200 mL at either Visit 1, Visit 1a, or Visit 1b; only 2 reversibility testing attempts are allowed.
• Demonstrate acceptable spirometry performance (ie, meet ATS/ERS acceptability/repeatability criteria).
• Willing and, in the opinion of the investigator, able to adjust current asthma therapy, as required by the protocol.
• Demonstrate acceptable MDI administration technique. Note: Use of a spacer device during the screening and randomized treatment periods is not permitted.
• Weight
• Body mass index < 40 kg/m2. Sex and Contraceptive/Barrier Requirements
• Contraceptive use by females should be consistent with local regulations regarding the methods of contraception for those participating in clinical studies.
• Female participants: A participant of childbearing potential, must have a negative urine pregnancy test at Visit 1 (to be read locally).
• Participants not of childbearing potential are defined as those who are physiologically incapable of becoming pregnant, including any participant who is 2 years postmenopausal, or surgically sterile (defined as having a bilateral oophorectomy, hysterectomy, tubal ligation, or other permanent birth control measures).
• Participants aged ≥ 50 years will be considered postmenopausal if they have been amenorrheic for 12 consecutive months or more following cessation of all exogenous hormonal treatment.
• Participants aged < 50 years will be considered postmenopausal if they have been amenorrheic for 12 consecutive months or more following cessation of exogenous hormonal treatment and in the absence of any alternative medical cause, as judged by the investigator.
• Participants of childbearing potential must use a highly effective form of contraception from signing of the ICF to 14 days after the last study intervention. Highly effective birth control methods are listed below:
• Total sexual abstinence is an acceptable method provided it is the usual lifestyle of the participant (defined as refraining from heterosexual intercourse during the entire period of risk associated with the study treatments).
• Combined (estrogen and progestogen containing) hormonal contraception associated with inhibition of ovulation):
• Oral
• Intravaginal (eg, NuvaRing®)
• Transdermal (eg, Evra Patch™, Xulane™)

You may not qualify if…

• 2 Exclusion Criteria
• Participants are excluded from the study if any of the following criteria apply:
• Medical Conditions and History
• Any evidence of chronic obstructive pulmonary disease or other significant lung disease (eg, chronic bronchitis, emphysema, bronchiectasis with the need of treatment, cystic fibrosis, or bronchopulmonary dysplasia). Significant is defined as any disease that, in the opinion of the investigator, would put the safety of the participant at risk through participation, or that could affect the efficacy or safety analysis.
• Life-threatening asthma defined as any history of significant asthma episode(s) requiring intubation associated with hypercapnia, respiratory arrest, hypoxic seizures, or asthma-related syncopal episode(s) within the last 5 years.
• Upper respiratory infection not resolved within 7 days of Visit 1 and throughout the screening period.
• Hospitalizations for asthma exacerbation within the last 3 months prior to Visit 1.
• Historical or current evidence of a clinically significant disease including, but not limited to: cardiovascular (eg, congestive heart failure, known aortic aneurysm, clinically significant cardiac arrhythmia, participants with known QTcF ≥ 480 ms, coronary heart disease), hepatic, renal, hematological, neuropsychological, endocrine (eg, uncontrolled diabetes mellitus, uncontrolled thyroid disorder, Addison's disease, Cushing's syndrome), or gastrointestinal (eg, poorly controlled peptic ulcer, gastroesophageal reflux disease). Significant is defined as any disease that, in the opinion of the investigator, would put the safety of the participant at risk through study participation, or that could affect the efficacy or safety analysis if the disease/condition exacerbated during the study.
• Cancer not in complete remission for at least 5 years prior to Visit 1. Note: Participants with squamous cell carcinoma of the skin or basal cell carcinoma of the skin or cervical carcinoma in situ are eligible, if in the opinion of the investigator, the condition has been adequately worked up and clinically controlled, and the participant's participation in the study would not represent a safety concern.
• Hospitalized for psychiatric disorder or attempted suicide within one year prior to Visit 1.
• History of psychiatric disease, intellectual deficiency, poor motivation, or other conditions limiting informed consent validity.
• Received a live attenuated vaccination within 7 days of Visit 1. Prior/Concomitant Therapy
• Oral/systemic corticosteroid use (any dose) within 6 weeks of Visit 1.
• Chronic use of oral corticosteroids (≥ 3 weeks use in the 3 months prior to Visit 1).
• Received any marketed (eg, omalizumab, mepolizumab, reslizumab) or investigational biologic within 3 months or 5 half-lives, whichever is longer, or any other medication specifically prohibited by the protocol within the indicated exclusionary time periods.
• Received tiotropium within 2 weeks of Visit 1.
• Received treatment for lower respiratory infection or asthma exacerbation within 6 weeks of Visit 1.
• Unable to abstain from protocol-defined prohibited medications during screening and the study.
• Using any herbal products by inhalation or nebulizer within 2 weeks of Visit 1 and does not agree to stop during the study duration.
• Prior/Concurrent Clinical Study Experience
• Treatment with investigational study intervention (or device) in another clinical study within the last 30 days or 5 half-lives, whichever is longer, prior to Visit 1.
• Hypersensitivity to β2-agonists or any component of the investigational MDI or any component of Ventolin Evohaler or HFA (or Pulmicort Flexhaler, if applicable).
• Other Exclusions
• Significant abuse of alcohol or drugs in the opinion of the investigator.
• Current smokers, former smokers with > 10 pack-years history, or former smokers who stopped smoking < 6 months (including all forms of tobacco, e-cigarettes [vaping], and marijuana).

Where it is running

• Research Site — Encinitas, California, United States
• Research Site — Lancaster, California, United States
• Research Site — Los Angeles, California, United States
• Research Site — Newport Beach, California, United States
• Research Site — San Diego, California, United States
• Research Site — San Jose, California, United States
• Research Site — Stockton, California, United States
• Research Site — Clearwater, Florida, United States
• Research Site — Miami, Florida, United States
• Research Site — Tallahassee, Florida, United States
• Research Site — Tampa, Florida, United States
• Research Site — White Marsh, Maryland, United States
• Research Site — Columbia, Missouri, United States
• Research Site — Saint Charles, Missouri, United States
• Research Site — St Louis, Missouri, United States
• Research Site — Raleigh, North Carolina, United States
• Research Site — Medford, Oregon, United States
• Research Site — Portland, Oregon, United States
• Research Site — Austin, Texas, United States
• Research Site — El Paso, Texas, United States
• Research Site — Victoria, Texas, United States
• Research Site — Milwaukee, Wisconsin, United States

Full record on ClinicalTrials.gov

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