Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
This combination therapy consists of an intranasal corticosteroid (INCS) and an oral antihistamine (OAH). Specifically, it involves the concurrent use of **fluticasone propionate** nasal spray and **azelastine hydrochloride** tablets. Fluticasone propionate is a synthetic glucocorticoid that acts as a potent anti-inflammatory agent by binding to the glucocorticoid receptor, thereby reducing the production of inflammatory mediators in the nasal mucosa. Azelastine hydrochloride is a second-generation H1-receptor antagonist that systemically blocks the action of histamine, a primary mediator of allergic responses. This specific regimen was evaluated in a Phase 4 clinical trial conducted by the **China-Japan Union Hospital** to compare its efficacy against a fixed-dose intranasal combination (INCS + INAH) in patients with moderate to severe allergic rhinitis.
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 fluticasone propionate + azelastine hydrochloride (oral).