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Clinical Trial Summary

This is a multicenter, open-label study to assess the safety and tolerability of VGL101 in subjects with documentation of a gene mutation in the CSF1R gene for the treatment of adult-onset leukoencephalopathy with axonal spheroids and pigmented glia (ALSP) and to evaluate the effects of VGL101 on imaging and biomarkers of disease progression in subjects with ALSP. Participants will receive infusions of VGL101 approximately every 4 weeks for 1 year. The study includes a 52-week, open-label Core Study, followed by a Long-Term Extension (LTE), which provides subjects who complete the original 52-week study (Core Study) with the option to continue treatment for up to an additional 2 years.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT05677659
Study type Interventional
Source Vigil Neuroscience, Inc.
Contact
Status Active, not recruiting
Phase Phase 2
Start date December 14, 2022
Completion date March 31, 2027

See also
  Status Clinical Trial Phase
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Enrolling by invitation NCT04503213 - A Study to Assess CSF1R-related Leukoencephalopathy After Stem Cell Transplantation
Active, not recruiting NCT02699190 - LeukoSEQ: Whole Genome Sequencing as a First-Line Diagnostic Tool for Leukodystrophies
Recruiting NCT03047369 - The Myelin Disorders Biorepository Project