Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
Regdanvimab is a recombinant human IgG1 monoclonal antibody developed for the treatment of COVID-19. It specifically targets the receptor binding domain (RBD) of the spike protein of SARS-CoV-2, blocking its interaction with the angiotensin-converting enzyme 2 (ACE2) receptor on host cells. By preventing this interaction, regdanvimab neutralizes SARS-CoV-2 and inhibits viral entry and replication within human cells. The drug is administered as a single intravenous infusion, typically within seven days of symptom onset in patients at risk for severe disease progression. Regdanvimab has been approved in South Korea and authorized in the European Union for adults with COVID-19 who do not require supplemental oxygen but are at increased risk of developing severe disease[1][3][4][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 regdanvimab.