drugset / Trial / NCT04513470

Allocetra-OTS in COVID-19

NCT04513470

Phase 1 Unknown 5 enrolled Hadassah Medical Organization
NaSingle-groupOpen-labelPrevention

Summary

This is a multi-center, open-label study evaluating the safety of Allocetra-OTS, in 5 subjects with severe COVID-19 and respiratory dysfunction. Subjects, who will be identified as suffering from COVID-19, will be recruited. After signing an informed consent by the patient and, within 24+6 hours following the time of eligibility (time 0), on Day 1, eligible recipient subjects will receive single intravenous (IV) administration of investigational product as described below. Subjects will be hospitalized for COVID-19, and later as medically indicated. Following investigational product (IP) administration (Day 1), subjects will be followed for efficacy and safety assessments through 28 days.

Timeline

Start
2020-08-01
Primary completion
2021-01
Completion
2021-02

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Allocetra-OTS Cell therapy 1.4e+08 cells/kg Intravenous

Indications