Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
NextFlo is a fixed-dose combination therapy delivered via a proprietary dry powder inhaler (DPI), primarily indicated for the maintenance treatment of asthma and chronic obstructive pulmonary disease (COPD). It consists of fluticasone propionate, a synthetic corticosteroid, and salmeterol xinafoate, a long-acting beta2-adrenergic agonist (LABA). Fluticasone propionate reduces airway inflammation by binding to glucocorticoid receptors, thereby inhibiting the production of multiple inflammatory cytokines and mediators. Salmeterol induces bronchodilation by selectively stimulating beta-2 adrenergic receptors on bronchial smooth muscle, leading to increased intracellular cyclic AMP and subsequent muscle relaxation. The NextFlo device itself is a multi-dose dry powder inhaler designed to provide consistent and accurate dose delivery across a wide range of patient inspiratory flow rates, ensuring effective deposition of the medication in the lungs.
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 NextFlo.