Overview
Clinical Trial With MSC for Graft Versus Host Disease Treatment
Status:
Active, not recruiting
Active, not recruiting
Trial end date:
2022-06-01
2022-06-01
Target enrollment:
0
0
Participant gender:
All
All
Summary
Sequential administration of MSCs obtained from adipose tissue is an effective and safe treatment for acute graft versus host disease refractory to first-line treatment. Furthermore the infusion of these cells produces a biological pattern in patients that relates to the clinical response.Phase:
Phase 1/Phase 2Accepts Healthy Volunteers?
NoDetails
Lead Sponsor:
Andalusian Initiative for Advanced Therapies - Fundación Pública Andaluza Progreso y SaludCollaborator:
Andalusian Initiative for Advanced Therapies
Criteria
Inclusion Criteria:1. Diagnosis of ≥ grade II Graft Versus Host Disease refractory to first-line treatment.
2. Having been subjected to hematopoietic Stem Cell Transplantation as treatment for
malignant blood disorder has been controlled by the transplantation. The source may
have been bone marrow cells or peripheral blood (PB) and coming from a family member
or unrelated donor.
3. Having been transplanted with myeloablative or non-myeloablative conditioning.
4. normal cardiac function (EF ≥ 40%) without evidence of uncontrolled hypertension,
congestive heart failure, angina pectoris or myocardial infarction within 6 months
prior to the process
5. Lung function without evidence of severe obstructive or restrictive lung disease.
6. Age between 18 and 65 years.
7. Women of childbearing age considered until one year after the last menstrual period
and which have not undergone a surgical sterilization must obtain a negative pregnancy
test at the time of inclusion in the study and commit to use a medically approved
birth control while on study.
8. normal cardiac function (EF ≥ 40%) without evidence of uncontrolled hypertension,
congestive heart failure, angina pectoris or myocardial infarction within 6 months
prior to the process.
9. Signature of informed consent -
Exclusion Criteria:
1. uncontrolled blood disorder by transplantation or progression at the time of
inclusion.
2. bacterial, viral, fungal or is not being controlled.
3. Any circumstance that the proposed trial dissuade medical treatment. Pregnancy,
lactation or refusal to use safe contraceptive measures.
4. Patients who are currently participating or have completed their participation in a
clinical trial in less than 3 months or who have participated in a clinical trial of
Advanced Therapies at any previous time period.
5. Patients who are currently participating or have completed their participation in a
clinical trial in a period shorter than 3 months or who have participated in a
clinical trial of Advanced Therapies at any previous time.
6. positive serology for Hepatitis B , Hepatitis C and AIDS Virus. -