Compares two inhalers taken as needed by teens with asthma
Tests budesonide/albuterol inhaler against albuterol inhaler in teens with asthma.
Plain-language title generated from the registry record
Registry title: Evaluating the Efficacy and Safety of PT027 Compared With PT007 Administered As Needed in Participants 12 to < 18 Years of Age With Asthma
Key facts
- Where
- Chihuahua City, Guadalajara, and Monterrey, MexicoSee the 3 sites
- Phase
- Phase 3
Could this be for you?
Answer for yourself. This is not a decision: only the study team can say whether you can take part.
- Are you between 12 and 17 years old?
Source: NCT06307665, who can take part
Where in Mexico
- Chihuahua CityChihuahua City, MexicoTaking people
- GuadalajaraGuadalajara, MexicoTaking people
- MonterreyMonterrey, MexicoTaking people
Questions to ask the study team
- How often do I need to come in, and for how long each time?
- Are travel costs paid?
- Can I keep my own doctor?
- What happens if I want to stop?
Trial details
- Who runs it
- AstraZeneca
- Trial code
- NCT06307665
- Record updated
- 10 November 2026
- Original description
The purpose of this study is to compare the effect of budesonide/albuterol metered-dose inhaler (BDA MDI) with albuterol sulfate metered-dose inhaler (AS MDI), both administered as needed, on the annualized rate of severe asthma exacerbations in adolescents with a documented clinical diagnosis of asthma and at least one severe exacerbation in the prior year.Read full original descriptionShow less
A Randomized, Double-blind, Multicenter, Parallel-group, Phase IIIb 52 Week Study Evaluating the Efficacy and Safety of PT027 Compared With PT007 Administered as Needed in Participants 12 to < 18 Years of Age With Asthma (ACADIA)
The purpose of this study is to compare the effect of budesonide/albuterol metered-dose inhaler (BDA MDI) with albuterol sulfate metered-dose inhaler (AS MDI), both administered as needed, on the annualized rate of severe asthma exacerbations in adolescents with a documented clinical diagnosis of asthma and at least one severe exacerbation in the prior year.
Inclusion: Confirmed clinical diagnosis of asthma at least 12 months; Receiving one of the following scheduled asthma maintenance therapies for at least 3 months with stable dosing for at least the last one month; Low-to-high-dose Inhaled corticosteroid(s) (ICS); Low-to-high-dose ICS or ICS/long-acting β2-agonist (LABA) with or without one additional maintenance therapy from the following: leukotriene receptor antagonist (LTRA), long-acting muscarinic antagonist (LAMA), or theophylline; Receiving inhaled short-acting β2-agonist (SABA) as needed; A documented history of at least one severe asthma exacerbation within 12 months; Use of Sponsor-provided albuterol sulfate inhalation aerosol medication; Demonstrate acceptable MDI administration technique as assessed by the investigator; use of spacers is prohibited; Able to perform acceptable and reproducible peak expiratory flow (PEF) measurements as assessed by the investigator; Participants must adhere to protocol specific contraception methods; Negative urine pregnancy test for participants of childbearing potential; Have a BMI < 40 kg/ m\^2; Capable of giving assent (signing the assent form) to participate in the study which includes compliance with the requirements and restrictions. The caregiver of the patient must be capable of giving written informed consent for the patient's participation in the study. Consent and assent forms must be completed prior to any study-specific procedures.
Exclusion: Experienced > 3 severe asthma exacerbations within 12 months before screening; Significant abuse of alcohol or drugs, in the opinion of the investigator; Oral corticosteroid(s) (OCS)/SCS use (any dose and any indication) within 4 weeks before Visit 1 or chronic use of OCS/SCS (≥ 3 weeks use in 3 months prior to Visit 1); 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); Completed treatment for lower respiratory infection and severe asthma exacerbation with SCS within 4 weeks of screening; Upper respiratory infection involving antibiotic treatment not resolved; Other significant lung disease, including regular or occasional use of oxygen; Historical or current evidence of a clinically significant disease including, but not limited to: cardiovascular, hepatic, renal, hematological, neuropsychological, endocrine, or gastrointestinal disorders; Cancer not in complete remission for at least 5 years; History or hospitalization for psychiatric disorder or attempted suicide within one year; Having a known or suspected hypersensitivity to albuterol/salbutamol, or budesonide and/or their excipients; 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); Use of any oral SABAs within one month.