Umbilical Cord Mesenchymal Stem Cells Therapy (19#iSCLife®-SA) for Patients With Spinocerebellar Ataxia
Starting soon · Phase 2
Conditions studied: Spinocerebellar Ataxia Type 1, Spinocerebellar Ataxia Type 2, Spinocerebellar Ataxia Type 3, Spinocerebellar Ataxia Type 6
In brief
The purpose of this study is verify the safety and efficacy of Human Umbilical Cord Mesenchymal Stem Cells (UC-MSC) therapy for patients with Spinocerebellar Ataxia, and in addition, explore the possible mechanisms of UC-MSC therapy in Spinocerebellar Ataxia.
Key facts
- Study ID
- NCT03378414
- Run by
- Sclnow Biotechnology Co., Ltd.
- People needed
- 45
- Starts
- 2026-12-31
- Expected to finish
- 2027-12-31
- Last updated by the study team
- 2026-04-23
Who can join
Age: 16 and older, up to 60. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Clinical and genomic test diagnoses as spinocerebellar ataxias (SCA) (include SCA 1, SCA 2, SCA 3, SCA 6), SARA (Scale for Assessment and Rating of Ataxia) score is 2-5, can complete 8-meter walking test(8MW)
- Do not receive stem cells treatment in 6 months
- Participants sign the consent form based on the experiment process and statement
You may not qualify if…
- Cardiac, renal, hepatic insufficiency; total bilirubin is 1.5 times higher than normal value, aspartate transaminase(AST)or alanine aminotransferase(ALT)is 2.5 times higher than normal value
- Hemogram: total white blood cells <3.0 * 10\^9 cells/L, blood platelet <75 * 10\^9/L, hemoglobin <100g/L
- pneumonia, or severe infection
- With severe allergic history
- Brain organic disorder, like brain tumor
- Serum with HIV, syphilis antibody positive
- Severe mental disease, cognitive disorder patients
- Other severe system or organ organic disease
- Pregnant, breast feeding, or planning pregnant women
- Participate other clinical experiments in 3 months
- With some other conditions that doctor propose not to participate
Full record on ClinicalTrials.gov
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