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Treatment of Knee Osteoarthritis With Autologous Mesenchymal Stromal Cell Product (RegStem)

Phase I Clinical Trial - Treatment of Knee Osteoarthritis With Autologous Mesenchymal Stromal Cell Product (RegStem)

Status
Completed
Phases
Phase 1
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03007576
Enrollment
12
Registered
2017-01-02
Start date
2017-08-01
Completion date
2019-08-31
Last updated
2019-11-13

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Osteoarthritis,Knee

Brief summary

Osteoarthritis (OA) is a common and incurable disease for the elderly in Taiwan, so it is an important mission to develop a new treatment for OA. Recently, cellular therapy is a new and popular medical treatment around the world, one of them is Mesenchymal Stromal Cells (MSCs). MSCs are found in many tissues of human body and play an important role for repairing, regeneration, anti-inflammatory and chondrogenesis. So, MSC product, RegStem, for osteoarthritis treatment becomes a developing target for new generation drugs. This study is to isolate and expand MSCs(RegStem) from infrapatellar fat pad of subject. When the number of MSCs expands to 1×10\^8, cell will be cryopreserved in the liquid nitrogen tank until all release tests passed. On the distribution day, cell will be thawed and injected into joint cavity of patient (5×10\^7). Subjects will be monitored after MSC product infusion of seven days, one month, six months and one year. The monitoring items include the changes of knee (by appearance, X-ray and MRI of knee) and pain improvement (by questionnaire).

Interventions

BIOLOGICALRegStem

RegStem, 1.5 ml, one injection

Sponsors

Far Eastern Memorial Hospital
CollaboratorOTHER
EMO Biomedicine Corporation
Lead SponsorINDUSTRY

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
50 Years to 75 Years
Healthy volunteers
No

Inclusion criteria

1. Subjects who understand and sign the informed consent form for this study 2. Grade 2\ 3 osteoarthritis according to the Kellgren-Lawrence grading scale with one-month X-ray 3. Age is 50\ 75 years old 4. Postmenopausal women 5. VAS scores in 50 to 90 mm

Exclusion criteria

1. Abnormal of liver and kidney: GOT and GPT \> 100 IU/L, BUN \>22 mg/dl and creatinine \> 1.2 mg/dl. 2. Positive serology for HIV, HTLV-1/2 and syphilis 3. Women who are pregnant or breast feeding 4. Serious pre-existing medical conditions: coagulation disorders, cardiovascular diseases (arrhythmias, myocardial infarction and surgery), renal diseases (chronic renal failure), liver diseases (cirrhosis), diabetes mellitus type I, cancer history. 5. Other joint diseases: knee deformity (knee varus greater than 10 degree or valgus greater than 20 degree), rheumatic arthritis, gouty arthritis, septic arthritis, serious meniscal tear, other autoimmune arthritis. 6. Skin inflammatory of knee 7. Knee pain caused by referred pain from spine disease or hip joint disease. Knee pain combined with pain from spine disease or hip disease. 8. Immunosuppressive state 9. Subjects who were injected with hyaluronic acid and PRP in the past 6 months 10. Body mass index (BMI) greater than 30 11. Have a history of allergic reaction of any medication 12. Participation in another clinical trial or treatment within 3 months 13. Other pathologic conditions or circumstances that difficult participation in this study according to PI's evaluations

Design outcomes

Primary

MeasureTime frameDescription
Safety of RegStem by incidence of adverse events and changes in physical examinations, vital signs and the results of clinical lab tests.48 weeks
Clinical assessment of International Knee Documentation Committee (IKDC) score48 weeksAssess symptoms of knee, sport activity and function of knee

Secondary

MeasureTime frame
Clinical assessment of Knee injury and Osteoarthritis Outcome Score (KOOS)48 weeks
Clinical assessment of visual analogue scale (VAS)48 weeks
Clinical assessment of knee X-ray48 weeks
Clinical assessment of knee MRI48 weeks

Countries

Taiwan

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026