Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
CCP2-University of North Carolina, Chapel Hill-COVID-19 refers to standard-titer COVID-19 convalescent plasma (CCP) evaluated in the CoronaVirus Inactivating Plasma (CoVIP) study (NCT04524507) at the University of North Carolina at Chapel Hill. This biologic therapy consists of plasma collected from individuals who have recovered from SARS-CoV-2 infection, containing polyclonal neutralizing antibodies. In the context of the IGHID 12021 phase 2 trial, CCP2 specifically designated the standard-titer arm, where the plasma units had neutralizing antibody titers between 1:160 and 1:640. The therapy works by providing passive immunity; the antibodies bind to the SARS-CoV-2 spike protein, preventing viral entry into host cells and facilitating viral clearance. The study was designed to compare the efficacy and safety of these standard-titer units against high-titer units in hospitalized adults with early COVID-19 symptoms.
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 standard-titer COVID-19 convalescent plasma.