Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
L-745,337 is a potent and highly selective inhibitor of cyclooxygenase-2 (COX-2), originally developed by Merck Frosst. It was designed as a non-steroidal anti-inflammatory drug (NSAID) candidate that could provide therapeutic benefits for inflammation and pain while avoiding the gastrointestinal toxicity typically associated with non-selective COX inhibitors like indomethacin. Research has demonstrated that L-745,337 effectively inhibits the production of pro-inflammatory prostanoids, such as PGE2 and PGI2, in human colonic mucosal biopsies from patients with inflammatory bowel disease (IBD). Although it served as a significant research tool in the development of the coxib class of drugs, it was not commercialized, as Merck ultimately prioritized other candidates such as rofecoxib (Vioxx).
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 L-745,337.