Mild-Moderate Asthma

Elegibility:
  • Are 12 years old or older
  • Have a diagnosis of asthma
  • Are capable of giving signed informed consent if ≥18 years of age. [Participants aged 12 to 17 years can provide assent, but a parent/legally acceptable representative must provide written consent before any trial procedures are performed.]
Descriptions:
This Phase 3 study is designed to evaluate the effectiveness and safety of an investigational asthma medication that combines two types of treatments: a fast-acting rescue medicine that works quickly during asthma symptoms and a long-acting medicine that helps reduce inflammation and swelling in the lungs over time. The investigational combination will be compared with three other study treatments: the fast-acting rescue medication alone (albuterol), the long-acting medication alone (a corticosteroid), and a placebo that looks like the study drug but contains no active ingredients. During the double-blind treatment period, participants will be randomly assigned, in equal numbers, to one of these four treatment groups. Neither participants nor study staff will know which treatment is assigned, helping to prevent bias. Participants will take two puffs of their assigned study treatment four times a day—early morning, midday, early evening, and at bedtime—as consistently as possible.

Join Study

Interested in participating in this study? Complete the form below to find out if you qualify. Once we receive your information, a member of our research team will contact you to review your eligibility and provide more details about the study. All information is kept confidential and protected under HIPAA regulations.

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