Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
LN2222 is an investigational small molecule prokinetic agent being developed by Shandong New Era Pharmaceutical, a subsidiary of Lunan Pharmaceutical Group. It is currently in Phase I clinical development in China for the treatment of postoperative gastrointestinal dysfunction (PGD). The drug is administered intravenously and is being evaluated for its safety, tolerability, and pharmacokinetics in comparison to oral prucalopride succinate. Based on this clinical comparison, LN2222 likely acts as a selective 5-hydroxytryptamine receptor 4 (5-HT4) agonist, a mechanism known to stimulate gastrointestinal motility and accelerate gastric emptying, which is critical for managing ileus and other forms of gastrointestinal dysfunction following surgery.
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 LN2222.