Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
zanamivir placebo + moxifloxacin placebo is a double-placebo control arm used in a Phase I clinical trial conducted by GSK. The study was a randomized, four-way crossover trial designed to evaluate the effect of intravenous (IV) zanamivir on cardiac conduction (specifically the QT interval) in healthy volunteers. In this specific treatment arm, participants received a single dose of an intravenous placebo (matching the IV zanamivir formulation) and a single dose of an oral placebo (matching the moxifloxacin positive control). This arm serves as the negative control to establish a baseline for cardiac conduction measurements and to validate the sensitivity of the study using moxifloxacin as a positive control. Zanamivir is a neuraminidase inhibitor developed for influenza, while moxifloxacin is a fluoroquinolone antibiotic commonly used as a positive control in Thorough QT (TQT) studies.
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 zanamivir placebo + moxifloxacin placebo.