Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
Placebo + ceftriaxone refers to a specific control arm in the INFUSE-Ceftriaxone Phase I clinical trial (NCT01290705) conducted by Baxter Healthcare Corporation. In this study arm, healthy volunteers received a subcutaneous injection of a placebo (0.9% sodium chloride) followed by a subcutaneous dose of ceftriaxone. This regimen served as a comparator to evaluate the safety and pharmacokinetics of subcutaneous ceftriaxone when administered with or without recombinant human hyaluronidase (Hylenex). Ceftriaxone is a broad-spectrum third-generation cephalosporin antibiotic that exerts its bactericidal effect by inhibiting bacterial cell wall synthesis through binding to penicillin-binding proteins (PBPs). The study aimed to establish the feasibility and maximum tolerated concentration of subcutaneous ceftriaxone administration.
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 placebo + ceftriaxone.