Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
Cefepime + zidebactam is a fixed-dose intravenous antibacterial combination marketed as **Zaynich**. It combines cefepime, a fourth-generation cephalosporin, with zidebactam, a beta-lactamase inhibitor and non-beta-lactam antibacterial beta-lactam enhancer. The agents act synergistically through complementary inhibition of bacterial penicillin-binding proteins, principally cefepime activity at PBP3 and high-affinity zidebactam activity at PBP2, with zidebactam also inhibiting susceptible serine beta-lactamases. In the United States, Zaynich was approved in 2026 for adult patients with complicated urinary tract infection, including pyelonephritis, caused by designated susceptible microorganisms. ([accessdata.fda.gov](https://www.accessdata.fda.gov/drugsatfda_docs/label/2026/220787Orig1s000lbl.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 cefepime + zidebactam.