Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
Hyperimmune intravenous immunoglobulin G specific to SARS-CoV-2, marketed as Covimmune™, is a polyclonal hyperimmune intravenous immunoglobulin (HIVIG) developed by the Australian company Aegros Ltd. It is produced from pooled human plasma collected from donors who have recovered from COVID-19 (convalescent plasma). The manufacturing process utilizes Aegros' proprietary HaemaFrac™ technology, a high-volume electrophoresis-based plasma fractionation method that achieves high purity and protein yield. The drug contains a concentrated solution of purified IgG antibodies with high titers of neutralizing antibodies against the SARS-CoV-2 virus. It is designed to provide immediate passive immunity for the prevention and treatment of COVID-19, particularly in vulnerable populations such as the immunocompromised or frontline workers. In the Phase 1/2 CHAT clinical trial, Covimmune™ demonstrated a fourfold increase in peak antibody levels compared to convalescent plasma and maintained a favorable safety profile.
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 hyperimmune intravenous immunoglobulin G specific to SARS-CoV-2.