Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
Xiangtong is a fully bioabsorbable drug-eluting sinus stent developed by Puyi (Shanghai) Biotechnology. Approved by the CFDA in 2017, it was the first product of its kind to be approved in China. The device is specifically designed for use in patients with chronic sinusitis who have undergone functional endoscopic sinus surgery (FESS). It consists of a biodegradable polymer scaffold that provides mechanical support to maintain the patency of the sinus ostia while locally eluting an anti-inflammatory corticosteroid. This localized drug delivery reduces mucosal inflammation and edema, thereby preventing the formation of postoperative adhesions and synechiae. Because the stent is fully biodegradable, it is naturally absorbed by the body over time, eliminating the need for a secondary surgical procedure for removal.
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 Xiangtong.