Clinical Trials Directory

Trials / Unknown

UnknownNCT04769245

The Effectiveness of ACB-IP 1.0 Convalescent Plasma in COVID-19 Infection

The Effectiveness of ACB-IP 1.0 Universal Pathogen Free Concentrated Cocktail Convalescent Plasma in COVID-19 Infection

Status
Unknown
Phase
Study type
Observational
Enrollment
40 (estimated)
Sponsor
Acibadem University · Academic / Other
Sex
All
Age
18 Years – 75 Years
Healthy volunteers

Summary

Pathogen-free, concentrated, pooled convalescent plasma has higher SARS-CoV2 antibody titers and neutralizing antibody activities, without requiring blood group compatibility that allows patient accessibility in a shorter time and has safe plasma characteristic.

Detailed description

The efficacy of SARS-CoV2 standard single donor convalescent plasma varied according to the application time and most importantly the amount of antibody that is administered. Single donor plasma has some drawbacks; such as the insufficient levels of neutralizing antibody activities, the requirements of blood group compatibility, and the risk of infection transmission. In this study, the efficacy and safety of pathogen inactivated, isohemagglutinin-depleted (concentrated) and pooled convalescent plasma was investigated.

Conditions

Timeline

Start date
2021-02-18
Primary completion
2021-04-01
Completion
2021-06-01
First posted
2021-02-24
Last updated
2021-02-24

Locations

2 sites across 1 country: Turkey (Türkiye)

Source: ClinicalTrials.gov record NCT04769245. Inclusion in this directory is not an endorsement.

The Effectiveness of ACB-IP 1.0 Convalescent Plasma in COVID-19 Infection (NCT04769245) · Clinical Trials Directory