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Clinical Trials/NCT01297972
NCT01297972CompletedPhase 1

Bone Marrow Mesenchymal Stem Cells in the Treatment of Refractory Severe Acquired Aplastic Anemia

University of Sao Paulo1 site in 1 country9 target enrollmentStarted: February 1, 2011Last updated:
Conditions

Trial Snapshot

Phase
Phase 1
Status
Completed
Enrollment
9
Locations
1
Primary Endpoint
Number of Participants with Adverse Events as a Measure of Safety and Tolerability of intravenous allogeneic unrelated mesenchymal stem cells infusion in patients with severe acquired aplastic anemia.

Study Overview

Brief Summary

Mesenchymal stem cells have been tested in many autoimmune disorders with encouraging results and may be an alternative to the treatment of immune-mediated severe acquired aplastic anemia.

Detailed Description

Acquired aplastic anemia is a bone marrow failure syndrome characterized by and empty bone marrow and low blood counts. Most of the cases are immune-mediated. Allogeneic bone marrow transplant is the preferable treatment modality for patients younger than 40 years with a matched sibling donor. Patients not eligible for transplant are treated with intensive immunosuppressive therapy often based on anti-thymocyte globulin and cyclosporine.

However, up to one third of patients treated with immunosuppression are refractory and one third of those who response eventually relapse. Refractory and relapsed cases may be the result of insufficient immunosuppression and these cases may benefit from additional immunosuppression. Mesenchymal stem cells infusion may be a potential treatment option, considering its properties to modulate the immune system.

Refractory or relapsed patients with aplastic anemia will be treated with conventional immunosuppressive regimen (anti-thymocyte globulin plus cyclosporine) combined with intravenous infusion of allogeneic unrelated bone marrow mesenchymal stem cells.

Study Design

Study Type
Interventional
Allocation
Na
Intervention Model
Single Group
Primary Purpose
Treatment
Masking
None

Eligibility Criteria

Ages
18 Years to 65 Years (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • •Diagnosis of Acquired Aplastic Anemia
  • •Relapse/refractory to at least 1 immunosuppressive first line treatment
  • •Not eligible to allogeneic bone marrow transplantation

Exclusion Criteria

  • •Previous or current malignancy
  • •Active or latent infectious disease
  • •Positive serologic tests for HIV, HCV, HBV, HTLV-1 and 2, Syphilis or Chagas disease
  • •Previous drug reaction for antithymocyte globulin, cyclosporin or corticosteroids
  • •Severe organic impairment (renal, hepatic, cardiac, pulmonary)
  • •Uncontrolled hypertension or diabetes
  • •Pregnancy
  • •Previous history of allergic reaction to penicillin or streptomycin
  • •Severe psychiatric disorder

Outcomes

Primary Outcomes

Number of Participants with Adverse Events as a Measure of Safety and Tolerability of intravenous allogeneic unrelated mesenchymal stem cells infusion in patients with severe acquired aplastic anemia.

Time Frame: After the mesenchymal stem cells infusion up to 6 mounth after

Adverse events like allergic reactions,infectious diseases,organ dysfunction or other related to mesenchymal stem cells infusion will be assessed.

Secondary Outcomes

  • Level of cytopenias(weekly until 6 months)
  • Transfusional requirements(weekly until 6 months)
  • Incidence of infections and febrile neutropenia(weekly until 6 months)

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Diego Villa Clé

MD

University of Sao Paulo

Study Sites (1)

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