Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
BDA MDI HFO is a fixed-dose combination drug-device product containing budesonide (an inhaled corticosteroid) and albuterol (a short-acting β2-adrenergic receptor agonist) delivered via a metered dose inhaler (MDI) that uses hydrofluoroolefin (HFO) as the propellant. This formulation is being developed as an as-needed rescue therapy for asthma, aiming to provide rapid symptom relief through albuterol while simultaneously reducing airway inflammation with budesonide. The use of HFO represents an environmentally friendlier alternative to traditional hydrofluoroalkane (HFA) propellants. The primary indication under investigation is asthma, where the combination seeks to reduce severe exacerbations by addressing both bronchoconstriction and underlying inflammation in response to worsening symptoms[1][2][3][4].
Beyond the preview
Explore the evidence, development activity, and competitive landscape with Gosset’s full data platform.
Follow clinical development from study design and recruitment through results.
Explore development by indication, patient population, and geography.
Trace asset ownership, licensing agreements, and commercial partnerships.
Explore the patent landscape and regulatory exclusivity around an asset.
Compare development programs by target, modality, and indication.
Connect source evidence and development news to your research questions.
See how Gosset can support your research on BDA MDI HFO.