Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
**Sulopenem etzadroxil + probenecid** is an oral fixed-dose antibacterial combination marketed in the United States as **Orlynvah**. Sulopenem etzadroxil is an orally absorbed penem prodrug that is converted to sulopenem, a beta-lactam antibacterial that binds bacterial penicillin-binding proteins and inhibits cell-wall synthesis. Probenecid inhibits renal organic anion transporter-mediated clearance of sulopenem, increasing systemic sulopenem exposure. The product is FDA-approved for uncomplicated urinary tract infections caused by susceptible *Escherichia coli*, *Klebsiella pneumoniae*, or *Proteus mirabilis* in adult women with limited or no alternative oral antibacterial options. ([accessdata.fda.gov](https://www.accessdata.fda.gov/drugsatfda_docs/label/2024/213972s000lbl.pdf))
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 sulopenem etzadroxil + probenecid.