Long-Term Follow-Up Study of Human Stem Cells Transplanted in Subjects With Connatal Pelizaeus-Merzbacher Disease (PMD)
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Purpose
The purpose of this study is to determine the long term safety and preliminary effect of HuCNS-SC cells transplanted in subjects with Connatal Pelizaeus-Merzbacher Disease (PMD).
| Condition | Intervention | Phase |
|---|---|---|
|
Pelizaeus-Merzbacher Disease PMD |
Biological: HuCNS-SC transplanted under protocol CL-N01-PMD |
Phase 1 |
| Study Type: | Observational |
| Study Design: | Observational Model: Cohort Time Perspective: Prospective |
| Official Title: | Long-Term Follow-Up Safety and Preliminary Efficacy Study of Human Central Nervous System Stem Cell (HuCNS-SC®) Transplantation in Subjects With Connatal Pelizaeus-Merzbacher Disease (PMD) |
- Incidence of serious adverse events (SAEs), results of physical and neurological examination, laboratory tests and vital signs. [ Time Frame: 4 years ] [ Designated as safety issue: Yes ]
- Preliminary efficacy using Bayley-III and Callier-Azusa Scale. [ Time Frame: 4 years ] [ Designated as safety issue: No ]Changes compared to baseline
- Changes in brain magnetic resonance imaging (MRI), electroencephalogram (EEG), seizure frequency and somato-sensory evoked potentials (SSEP). [ Time Frame: 4 years ] [ Designated as safety issue: No ]Changes compared to baseline
| Estimated Enrollment: | 4 |
| Study Start Date: | June 2011 |
| Estimated Study Completion Date: | June 2016 |
| Estimated Primary Completion Date: | February 2016 (Final data collection date for primary outcome measure) |
| Groups/Cohorts | Assigned Interventions |
|---|---|
| Observation |
Biological: HuCNS-SC transplanted under protocol CL-N01-PMD
Long term follow-up observation of subjects who received transplant during the initial pahse of the study.
Other Name: Follow-up
|
Detailed Description:
Only subjects who underwent HuCNS-SC transplantation under Protocol CL-N01-PMD will be enrolled in this long term follow-up study.
Subjects will return to the site six months and one year after completion of the Phase I study and then annually for a total study duration of four years. Phone calls will also be made by the Investigator to the subject's parent/legal guardian bi-annually to conduct a phone visit through the four-year duration of the study.
Eligibility| Genders Eligible for Study: | Male |
| Accepts Healthy Volunteers: | No |
| Sampling Method: | Non-Probability Sample |
PMD Subjects who underwent transplantation of HuCNS-SC cells under CL-N01-PMD study
Inclusion Criteria:
- Subjects who received HuCNS-SC cells under Protocol CL-N01-PMD
Exclusion Criteria:
- Subjects who received off-protocol immunosuppressive medications.
- Subjects who are concurrently enrolled in another investigational study.
Contacts and Locations
More Information
No publications provided
| Responsible Party: | StemCells, Inc. |
| ClinicalTrials.gov Identifier: | NCT01391637 History of Changes |
| Other Study ID Numbers: | CL-N02-PMD |
| Study First Received: | July 6, 2011 |
| Last Updated: | November 7, 2012 |
| Health Authority: | United States: Food and Drug Administration |
Keywords provided by StemCells, Inc.:
|
Long term follow-up HuCNS-SC cells human central nervous system stem cells |
Additional relevant MeSH terms:
|
Pelizaeus-Merzbacher Disease Hereditary Central Nervous System Demyelinating Diseases Brain Diseases, Metabolic, Inborn Brain Diseases, Metabolic Brain Diseases Central Nervous System Diseases Nervous System Diseases |
Leukoencephalopathies Demyelinating Diseases Genetic Diseases, X-Linked Genetic Diseases, Inborn Metabolism, Inborn Errors Metabolic Diseases |
ClinicalTrials.gov processed this record on May 16, 2013