Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
GLA-AF (glucopyranosyl lipid adjuvant-aqueous formulation) is a synthetic vaccine adjuvant designed to enhance immune responses to vaccines, particularly for intradermal and mucosal administration. It is an emulsion-free aqueous formulation of the synthetic Toll-like receptor 4 (TLR4) agonist known as glucopyranosyl lipid adjuvant (GLA). GLA-AF has been shown in preclinical and clinical studies to safely boost both humoral and cellular immune responses when co-administered with various antigens, including influenza and HIV vaccine candidates. Its mechanism of action involves activation of TLR4 on antigen-presenting cells, leading to enhanced Th1-type immunity and increased antibody titers. The development of GLA-AF addresses the need for potent, safe intradermal or mucosal vaccine adjuvants that can be self-administered or used in pandemic scenarios[1][2][8].
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 glucopyranosyl lipid adjuvant-aqueous formulation.