Trial | NCT03847844  Report issue

Title

UCMSCs as Front-line Approach of Treatment for Patients With aGVHD
Cytopeutics® Umbilical Cord Mesenchymal Stem Cells (Cyto-MSC) for Patients With Grade II -IV Acute Graft-Versus-Host Disease: A Phase I/II Clinical Study

  • Phase

    Phase 1/Phase 2

  • Study Type

    Interventional

  • Status

    Unknown status

  • Study Participants

    40
Background: Graft-versus-host disease (GVHD) is a devastating complication following allogeneic hematopoietic stem cell transplantation (HSCT) mediated by stimulation of antigen presenting cells (APCs) which leads to donor T-lymphocytes activation and target tissue destruction, particularly affecting the skin, gastrointestinal tract, and liver in acute setting. In recent years, researchers have discovered that the application of mesenchymal stromal cells (MSCs) as salvage treatment among steroid refractory GVHD patients improves outcomes without long-term risk association. On the other hand, the use of MSCs concurrently with steroids as front-line treatment for acute GVHD has yet to be researched on. The investigators hypothesize that this approach, as the MSCs will be administered at earlier stage of the disease, will increase survival rate and reduce mortality among aGVHD patients.

Objective: In this study, the investigators aim to determine the efficacy and safety of allogeneic infusion of Cytopeutics® umbilical cord-derived mesenchymal stromal cells (Cyto-MSC) in combination of standard corticosteroid therapy as front-line approach for treatment of grade II-IV acute GVHD patients.

Study design: This is a phase I/II clinical study involving patients who underwent an allogeneic HSCT for malignant or non malignant haematological disorders and developed grade II-IV acute GVHD. A total of 40 eligible patients will be recruited in this study.

For Phase I open labelled study, 5 eligible patients will be recruited to receive Cyto-MSC (5 million UC-MSCs per kg bodyweight) and standard treatment. Meanwhile, for Phase II double blinded placebo controlled study, another 35 eligible patients will be recruited and randomized into 2 study groups where 15 patients will be assigned into Group A to receive Cyto-MSC (5 million UCMSCs per kg bodyweight) and standard treatment, meanwhile another 20 patients will be assigned into Group B to receive Placebo and standard treatment.

Cyto-MSC or Placebo will be administered at Day 1 and Day 4. Another infusion of Cyto-MSC or Placebo will be given at Day 7 if the patient shows no or partial response based on GvHD grading criteria. All patients will be assessed up until 6 months follow-up which include medical history, clinical and physical evaluations, pathology investigations, biomarkers and immune cell subsets analysis, as well as quality of life questionnaires.
Study Started
Feb 01
2019
Primary Completion
Oct 31
2021
Anticipated
Study Completion
Dec 31
2021
Anticipated
Last Update
Jul 15
2020

Biological Umbilical cord derived mesenchymal stem cell

Umbilical cord derived mesenchymal stem cell

  • Other names: Cyto-MSC

Other Placebo

Normal saline

Group A Experimental

Cyto-MSC (5 million UCMSCs per kg bodyweight) and standard treatment

Group B Placebo Comparator

Placebo (normal saline) and standard treatment

Criteria 

Inclusion Criteria:

Patient age 16 and above
Patient who has undergone an allogeneic haematopoietic stem cell transplantation (HSCT) receiving allograft either from HLA-matched related donor (MRD), HLA-matched unrelated donor (MUD), Unrelated Cord Blood (UCB) or Haploidentical donor and developed grade II-IV acute graft versus host disease (acute GVHD) involving the skin, GI tract and/or liver based on 1994 Consensus Conference on Acute GVHD Grading
Patient and/or parent(s) or legal guardian(s) and assent form signed informed consent. Assent form will be obtained for patients aged less than 18 years. Investigators will obtain the permission of the parents or guardians for the participation of the minor in the research, and to solicit assent from the minor

Exclusion Criteria:

Patient who has enrolled in another investigational drug trial or stem cell related trial or has completed the aforesaid within (3) months
Patient with HIV or syphilis (Patient should be screened for HIV and VDRL up to 6 months prior to study start)
Patient with Hepatitis B (HBV) or Hepatitis C (HCV). All patients must be screened for HBV and HCV up to 6 months prior to study start using the routine hepatitis virus laboratory. Patients who are positive for HBsAg or HBcAb will be eligible if they are negative for HBV-DNA, these patients should receive prophylactic antiviral therapy. Patients who are positive for anti-HCV antibody will be eligible if they are negative for HCV-RNA
Patient has creatinine clearance of ≤50mL/min or creatinine is ≥200 µmol/L
Patient had undergone or on other immune-modulatory treatments such as interferon or Thalidomide over the last 12 months
Patient with progressive underlying disease or not in complete remission (CR) at the time of transplant
Any other severe co-morbidities which the doctor deems as a contraindication to cell therapy
Adults under law protection or without ability to consent
The patient has previous history or on-going psychiatric illness
Patient has received an HSCT transplant for a solid tumor disease
Patient has a known hypersensitivity to dimethyl sulfoxide (DMSO)
Patient is a female who is pregnant, lactating, or is planning a pregnancy during study participation, or in the follow-up period
No Results Posted