Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
Longacef suspensión is an oral antibiotic formulation containing cefixime, a third-generation cephalosporin. Developed and marketed by Megat Pharmaceutical in Ecuador, it is provided as a powder for oral suspension (100 mg/5 ml) primarily intended for pediatric use. Cefixime is a small molecule drug that exerts its bactericidal effect by binding to penicillin-binding proteins (PBPs) located in the bacterial cell wall. This binding inhibits the final transpeptidation step of peptidoglycan synthesis, leading to cell wall lysis and bacterial death. Longacef is indicated for the treatment of various bacterial infections, including acute bronchitis, pneumonia, otitis media, pharyngitis, tonsillitis, and uncomplicated urinary tract infections, and is noted for its stability against many beta-lactamase enzymes.
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 Longacef suspensión.