Autologous Adipose Derived Mesenchymal Stem Cells for Spinal Cord Injury Patients

Launched by MAYO CLINIC · Aug 18, 2020

Keywords

ClinConnect Summary

This clinical trial is exploring a new treatment for people with spinal cord injuries. Specifically, the study is looking at the safety and potential benefits of using stem cells taken from the patient’s own fat. These stem cells will be injected into the spinal space to see if they can help improve function and recovery after a spinal cord injury.

To be eligible for this trial, participants must be at least 18 years old and have a specific type of spinal cord injury. They should have a grade A or B injury, meaning they have severe impairment, but may have seen some improvement within a year. Participants will need to go through several procedures, including fat harvesting and follow-up visits, and will be monitored closely throughout the study. It’s essential for potential participants to understand the requirements and risks, and they will need to give their written consent before joining the trial. This study is currently recruiting participants of all genders aged 18 and older.

Gender

ALL

Eligibility criteria

• Inclusion Criteria:
• • Male or female aged 18 years and older
• • Females of childbearing potential must have a negative pregnancy test prior to receiving the study drug and will agree to use adequate contraception (hormonal/barrier method or abstinence) from the time of screening to a period of 1 year following completion of the drug treatment cycle. Females of childbearing potential are defined as premenopausal and not surgically sterilized, or post-menopausal for fewer than 2 years. If the urine pregnancy test is positive, the study drug will not be administered and the result will be confirmed by a serum pregnancy test. Serum pregnancy tests will be performed at a central clinical laboratory, whereas urine pregnancy tests will be performed by qualified personnel using kit.
• • Females becoming pregnant during the study will continue to be monitored for the duration of the study or completion of the pregnancy, whichever is longer. Monitoring will include perinatal and neonatal outcome. Any SAEs associated with pregnancy will be recorded.
• • AIS grade A or B of SCI at the time of injury with or without subsequent improvement within 1 year of injury that has progressed to a higher AIS grade with a plateau in functional improvement
• • SCI must be traumatic, blunt/non-penetrating in nature and not degenerative
• • Full understanding of the requirements of the study and willingness to comply with the treatment plan, including fat harvesting, laboratory tests, diagnostic imaging, complete physical and neurologic examination and follow-up visits and assessments
• • Full understanding of the requirements of home exercise program prescribed by physical and occupational therapists.
• • Once the nature of the study is fully explained and prior to any study-related procedure is initiated the subject is willing to provide written, informed consent and complete HIPAA documentation
• Exclusion Criteria:
• • Pregnant or nursing, or planning on becoming pregnant during the study period
• • AIS grade of SCI other than A or B at the time of injury
• • Non-traumatic SCI
• • History of receiving mesenchymal stem cell, gene or exosome therapy for any indications
• • History of intra-spinal infection
• • History of superficial infection in the index spinal level within 6 months of study
• • Evidence of current superficial infection affecting the index spinal level at the time of enrollment
• • On chronic, immunosuppressive transplant therapy or having a chronic, immunosuppressive state, including use of systemic steroids/corticosteroids
• • Taking anti-rheumatic disease medication (including methotrexate or other antimetabolites) within 3 months prior to study enrollment
• • Ongoing infectious disease, including but not limited to tuberculosis, HIV, hepatitis, and syphilis
• • Fever, defined as temperature above 100.4 F/38.0 Celsius, or mental confusion at baseline
• • Significant improvement between the time of adipose tissue harvest and the time of injection, defined as improvement from AIS grade A or B to AIS grade C or greater.
• • Clinically significant cardiovascular (e.g. history of myocardial infarction, congestive heart failure or uncontrolled hypertension \> 90 mmHg diastolic and/or 180 mmHg systolic), neurological (e.g. stroke, TIA) renal, hepatic or endocrine disease (e.g. diabetes, osteoporosis).
• • History of malignancy including melanoma with the exception of localized skin cancers (with no evidence of metastasis, significant invasion, or re-occurrence within three years of baseline). Any other malignancy will not be allowed.
• • History of blood dyscrasia, including but not limited to anemia, thrombocytopenia, and monoclonal gammopathy
• • Participation in a study of an experimental drug or medical device within 3 months of study enrollment
• • Known allergy to local anesthetics of other components of the study drug
• • Any contraindication to MRI scan according to MRI guidelines, or unwillingness to undergo MRI procedures
• • History of or current evidence of alcohol or drug abuse or dependence, recreational use of illicit drug or prescription medications, or use of medical marijuana within 30 days of study entry
• • Diagnosis of schizophrenia or bipolar disorder
• • Patients with baseline depression, diagnosed by the Beck Depression Inventory Assessment
• • Currently taking riluzole for treatment of amyotrophic lateral sclerosis (ALS)