Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
LY900021 is a subcutaneous co-formulation developed by Eli Lilly and Company, consisting of the interleukin-23 (IL-23) inhibitor mirikizumab (LY3074828) and recombinant human hyaluronidase (rHuPH20). Mirikizumab is a humanized IgG4 monoclonal antibody that selectively targets the p19 subunit of IL-23, thereby blocking the IL-23/IL-17 inflammatory axis which is central to the pathogenesis of several autoimmune conditions. The inclusion of rHuPH20, a Halozyme ENHANZE technology component, serves to transiently degrade hyaluronan in the extracellular matrix of the subcutaneous tissue. This action increases tissue permeability, allowing for the administration of larger volumes of the therapeutic antibody and potentially improving patient comfort and absorption. LY900021 is primarily being investigated for the treatment of ulcerative colitis, Crohn's disease, and plaque psoriasis.
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 LY900021 (Eli Lilly and Company).