Viewing Study NCT05682560


Ignite Creation Date: 2025-12-25 @ 2:04 AM
Ignite Modification Date: 2025-12-27 @ 11:37 PM
Study NCT ID: NCT05682560
Status: COMPLETED
Last Update Posted: 2025-03-24
First Post: 2023-01-11
Is NOT Gene Therapy: True
Has Adverse Events: False

Brief Title: Human Umbilical Cord Blood (RegeneCyte) Infusion in Patients with Post-COVID Syndrome
Sponsor: StemCyte, Inc.
Organization:

Study Overview

Official Title: A Randomized Controlled Phase IIa, Two-arm Study to Assess the Safety and Efficacy of Human Umbilical Cord Blood (RegeneCyte) Infusion in Patients with Post-COVID Syndrome
Status: COMPLETED
Status Verified Date: 2025-03
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: REGENECYTE (HPC, Cord Blood, hUCB) for treatment in patients with post-COVID.
Detailed Description: This is a two-arm, single-center, single-blind, randomized, placebo-controlled phase IIa study. A total of 30 subjects with post-COVID will be enrolled.

Study Oversight

Has Oversight DMC: True
Is a FDA Regulated Drug?: True
Is a FDA Regulated Device?: False
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: False
Is an FDA AA801 Violation?: