Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
This antibiotic regimen consists of a combination of cefazolin and cephalexin administered as prophylaxis to prevent postoperative infections following cardiac implantable electronic device (CIED) implantation. Developed and studied by National Cheng-Kung University Hospital in the ABxFREE trial, the protocol involves standard pre-procedural prophylaxis followed by a one-day intravenous course of cefazolin and a subsequent three-day oral course of cephalexin. Both agents are first-generation cephalosporins that inhibit bacterial cell wall synthesis by binding to penicillin-binding proteins (PBPs), providing coverage against common surgical site pathogens such as *Staphylococcus aureus*. The regimen is specifically designed to evaluate whether extended post-procedural prophylaxis reduces infection rates compared to standard pre-procedural dosing alone.
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 cefazolin + cephalexin.