Clinical Trials Directory

Trials / Completed

CompletedNCT03257098

Allogeneic ABCB5-positive Stem Cells for Treatment of CVU

An Interventional, Single Arm, Multicenter, Phase I/IIa Clinical Trial to Investigate the Efficacy and Safety of Allo-APZ2-CVU on Wound Healing of Chronic Venous Ulcer (CVU)

Status
Completed
Phase
Phase 1 / Phase 2
Study type
Interventional
Enrollment
31 (actual)
Sponsor
RHEACELL GmbH & Co. KG · Industry
Sex
All
Age
35 Years – 85 Years
Healthy volunteers
Not accepted

Summary

The aim of this clinical trial is to investigate the efficacy (by monitoring the wound size reduction of Chronic Venous Ulcers) and safety (by monitoring adverse events) of the medicinal product to be studied after two applications on the wound surface in patients with Chronic Venous Ulcers.

Detailed description

This is an interventional, single arm, phase I/IIa clinical trial to investigate the efficacy and safety of allogeneic ABCB5-positive mesenchymal stem cells (MSCs) on wound healing in patients with chronic venous ulcer (CVU). Allogeneic MSCs will be isolated ex vivo and will be expanded in vitro. The IMP incorporating the ABCB5-positive MSCs will then be applied on the wound surface of CVU under local anesthesia (on Day 0 and Week 6.1). Wound measurements from Visit (V) 2 and V9 will be used to determine the cell amount for the IMP treatments on V3 and V10, respectively. Patients are followed up for efficacy for 3 months which allows to distinguish actual wound healing from transient wound coverage. The wound healing process will be documented by standardized photography. The wound size evaluation will start on the day of the first change of wound dressing. The quality of the wound healing process will be assessed on the basis of formation of granulation tissue, epithelialization and wound exudation. Pain will be assessed using a numerical rating scale and quality of life will be investigated with standardized and validated questionnaires. To assess long-term safety of allo-APZ2-CVU three follow-up visits at Months 6, 9 and 12 after the first IMP applications are included.

Conditions

Interventions

TypeNameDescription
BIOLOGICALallo-APZ2-CVUSuspension of ABCB5-positive mesenchymal stem cells

Timeline

Start date
2017-11-16
Primary completion
2020-06-25
Completion
2020-06-25
First posted
2017-08-22
Last updated
2020-09-10

Locations

9 sites across 1 country: Germany

Source: ClinicalTrials.gov record NCT03257098. Inclusion in this directory is not an endorsement.