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NEALS Clinical Poster #23, entitled “MicroRNA Changes in the NurOwn® Phase 2 ALS Randomized Clinical Trial: Relationship to Neuroprotection and Innate Immunity.”
- Presenter:
James Berry M.D ., MHSc,Massachussetts General Hospital - Key Academic Collaborators:
Massachusetts General Hospital :James Berry , M.D. and Merit Cudkowicz, M.D.University of Massachusetts :Robert Brown , M.D. and Margaret Ayo Owegi, D.O.Mayo Clinic :Anthony Windebank , M.D. andNathan Staff , M.D., Ph.D.
- Objective:
- To relate CSF miRNA changes to CSF biomarkers of apoptosis and innate immune activation in pre- and 2-weeks post-intrathecal (IT) transplantation of MSC-NTF cells in a NurOwn® Phase 2 trial (NCT02017912).
- Conclusions
- The biomarker data demonstrated increases in miRNA 132 and miRNA 146a and statistically significant decreases in MCP-1, SDF-1, CHIT-1 and Caspase-3 levels in CSF following a single MSC-NTF cell transplantation in the NurOwn® Phase 2 trial.
- The data presented suggests that miRNA secreted by MSC-NTF cells may contribute to CSF biomarker evidence of neuroprotection and immunomodulation.
- Additional miRNA evaluation and biomarker correlations will be examined in the ongoing NurOwn® Phase 3 pivotal trial in ALS (NCT03280056).
- For more information: https://goo.gl/zikHA2
About
About NurOwn® Phase 3 Clinical Program in ALS
BrainStorm is currently enrolling a Phase 3 pivotal trial investigating repeat-administration of NurOwn® in ALS at six clinical sites in the U.S., supported by a grant from the
About U.S. Sites for NurOwn® Phase 3 Trial in ALS
University of California Irvine ; Principal Investigator:Namita Goyal , M.D.Cedars-Sinai Medical Center ; Principal Investigator:Robert Baloh , M.D.California Pacific Medical Center ; Principal Investigator:Robert Miller , M.D.Massachusetts General Hospital ; Principal Investigator:James Berry , M.D.University of Massachusetts Medical School ; Principal Investigator:Robert Brown , M.D.Mayo Clinic ; Principal Investigator:Anthony Windebank , M.D.
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uri@brainstorm-cell.com
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