Overview

Study of FT516 for the Treatment of COVID-19 in Hospitalized Patients With Hypoxia

Status:
Active, not recruiting
Trial end date:
2022-01-01
Target enrollment:
Participant gender:
Summary
This is a Phase I study with the primary objective of identifying the maximum tolerated dose (MTD) of FT516 using 3 dose-escalation strategies (number of doses and cell dose) for the treatment of coronavirus disease 2019 (COVID-19). This study provides initial estimates of safety and efficacy based on stable respiratory function, as well as, determining the feasibility for full-scale studies designed both for efficacy and safety.
Phase:
Phase 1
Details
Lead Sponsor:
Masonic Cancer Center, University of Minnesota