Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
Inactivated convalescent plasma (National Blood Center Foundation/Hemolife) is a biologic therapy consisting of plasma collected from recovered COVID-19 patients. The plasma is treated with riboflavin (vitamin B2) and ultraviolet (UV) light using the Mirasol Pathogen Reduction Technology system to inactivate potential viral particles, including SARS-CoV-2, while preserving the functional integrity of neutralizing antibodies. These antibodies target the SARS-CoV-2 spike protein and its receptor-binding domain (RBD), thereby providing passive immunity and inhibiting viral attachment to host cells. This therapeutic approach has been evaluated in Phase 2 clinical trials for hospitalized COVID-19 patients presenting with severe conditions such as pneumonia, acute respiratory distress syndrome (ARDS), or sepsis.
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 inactivated convalescent plasma.