Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
Equine immunoglobulin anti SARS-CoV‑2 is a passive immunotherapy product consisting of polyclonal antibodies derived from the plasma of horses that have been hyperimmunized with inactivated or recombinant antigens from the SARS-CoV‑2 virus, including spike protein (S1), receptor binding domain (RBD), nucleocapsid, and other viral proteins. The preparation typically involves enzymatic digestion to produce F(ab')₂ fragments, removing the Fc region to reduce adverse reactions while retaining strong neutralizing activity. These antibodies exhibit high titers and broad neutralization capacity against multiple variants of concern and interest, including Delta and Omicron lineages. The therapy is designed for intravenous administration as a treatment for moderate to severe COVID‑19 cases, especially where monoclonal antibody therapies may be less accessible or effective due to variant escape. Clinical studies indicate good tolerability and potential efficacy in reducing disease severity[[1]][[3]][[5]].
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 equine immunoglobulin anti SARS-CoV-2.