Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
Anifrolumab is a fully human IgG1κ monoclonal antibody used as an add-on treatment for adults with moderate to severe systemic lupus erythematosus (SLE) who are receiving standard therapy. It works by selectively binding to subunit 1 of the type I interferon receptor (IFNAR1), thereby blocking the activity of all type I interferons, including IFN-α, IFN-β, and IFN-ω. This blockade inhibits downstream inflammatory signaling and gene expression associated with SLE pathogenesis. Anifrolumab also induces internalization of IFNAR1, further reducing receptor availability on cell surfaces. The Fc region contains three mutations (L234F/L235E/P331S) to reduce effector functions such as antibody-dependent cellular cytotoxicity. Developed by MedImmune/AstraZeneca, it was first approved in the US in July 2021 and is considered a first-in-class medication for SLE[2][3][5][6].
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 anifrolumab.