Allogeneic Human Mesenchymal Stem Cell Injection in PAtieNts With FaceTogenic Back Pain (VALIANT)

This is an interventional treatment trial for Facetogenic Back Pain focused on measuring stem cells, back pain Read More

Inclusion Criteria:

In order to participate in this study, a subject must:

1. Provide written informed consent.
2. Subjects age >18 and <75 years at the time of signing the Informed Consent Form.

3. Facetogenic back pain diagnosed using the following diagnostic criteria:

   • The facet joint may be affected by systemic disease, as rheumatoid arthritis and ankylosing spondylitis, or be site of micro traumatic fractures, osteoarthritis, meniscoid entrapment, synovial impingement, joint subluxation, synovial inflammation, loss of cartilage, and mechanical injury.
   • Pain onset at dorsal extension and release at flexion is often considered suggestive for facet pain, even if non-specific, such as maximal tenderness upon deep palpation of posterior elements
   • History of temporary improvement with a medial branch block anesthetic injection of the targeted joints
   • Axial lumbar pain without radicular symptoms
   • Pain on hyperextension, rotation, and lateral bending with physical exam
4. Chronic facetogenic pain (≥ 6 months) in patients that have failed conservative management. (This includes but is not limited to a trial of oral medications, 6 weeks of physical therapy, intra-articular injection of the facet joints, and/or facet joint medial branch neurotomy.)
5. Diagnosis of lumbar facet joint pain confirmed by analgesic injections.
6. Have spinal level L3-4, L4-5 and L5-S1 bilaterally for bilateral pain and same side only for unilateral pain.

Exclusion Criteria:

In order to participate in this study, a subject must not:

1. Previous surgical intervention for back pain
2. Previous mesenchymal stem cell (MSC) injection(s) in to facet joints
3. Use of anticoagulation or NSAIDs within 5 days of the injection
4. MRI finding of severe high grade lumbar stenosis
5. Leg pain exceeding back pain
6. Pain worse with flexion maneuvers
7. Fracture of lumbar vertebrae
8. Be a female who is pregnant, nursing, or of childbearing potential while not practicing effective contraceptive methods. Female subjects must undergo a blood or urine pregnancy test at screening and within 36 hours prior to injection.
9. Inability to perform any of the assessments required for endpoint analysis.
10. Clinically abnormal screening laboratory values.
11. Serious comorbid illness or any other condition that, in the opinion of the investigator, may compromise the safety or compliance of the subject or preclude successful completion of the study.
12. Hypersensitivity to dimethyl sulfoxide (DMSO).
13. Be an organ transplant recipient.
14. Have a clinical history of malignancy within 5 years (i.e., subjects with prior malignancy must be disease free for 5 years), except curatively-treated basal cell carcinoma, squamous cell carcinoma, melanoma in situ or cervical carcinoma, if recurrence occurs.
15. Have a non-pulmonary condition that limits lifespan to < 1 year.
16. Have a history of drug or alcohol abuse within the past 24 months.
17. Be serum positive for HIV, hepatitis BsAg or Viremic hepatitis C.
18. Be currently participating (or participated within the previous 30 days) in an investigational therapeutic or device trial.