Convalescent Plasma To Limit COVID-19 Associated Complications

Status Not yet recruiting

Clinical Trial Summary

This is a randomized, blinded phase 2 trial to assess the efficacy and safety of anti-SARS-CoV-2 convalescent plasma in hospitalized patients with a symptom onset between 3 and 7 days OR within 72 hours of hospitalization.

Clinical Trial Description

Yale University is conducting this trial as a single site in collaboration with the New York University protocol. That trial is registered separately in ClinicalTrials.gov (NCT04364737), with Einstein College of medicine listed as a collaborator. Yale has applied for its own IND, which is pending at the time of this registration. Yale will be using the same data capture system and central COVID specific-data safety monitoring board (DSMB) as the other sites. ;

Study Design

Related Conditions & MeSH terms

Corona Virus Infection
Coronavirus Infections
Severe Acute Respiratory Syndrome

Clinical Trial Details

NCT number	NCT04404634
Study type	Interventional
Source	Yale University
Contact	Mahalia Desruisseaux, MD
Phone	203-737-4057
Email	mahalia.desruisseaux@yale.edu
Status	Not yet recruiting
Phase	Phase 2
Start date	May 2020
Completion date	January 2023

View Details

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