Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
AID351 is a **human anti-dengue virus monoclonal antibody** engineered for broad neutralizing activity against all four dengue virus serotypes (DENV-1 to DENV-4). Originally discovered by A*STAR SIgN and NUS, it was optimized by Chugai Pharmaceutical using proprietary antibody engineering technologies, including affinity maturation of the Fab region and Fc modifications (LALA/KAES) to abrogate Fcγ receptor binding—reducing antibody-dependent enhancement (ADE) risk—while preserving or enhancing C1q binding for complement-mediated antiviral efficacy. It demonstrates therapeutic potential in mouse models by reducing viremia, mitigating thrombocytopenia, and improving survival post-DENV-2 infection, with favorable pharmacokinetics including extended half-life and good subcutaneous bioavailability in cynomolgus monkeys. Primarily developed for **prevention and treatment of dengue fever**, an infectious disease affecting nearly 400 million annually, AID351 is in **preclinical development** with a recent collaboration between Chugai and GSK's Global Health Unit to advance toward clinical studies.[1][2][3]
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 AID351.