D-Cycloserine for Serine Palmitoyltransferase Inhibition
Part of paid clinical trials in Boston, Massachusetts.
- Sponsor
- Massachusetts General Hospital
- Study ID
- NCT07542548
- Phase
- PHASE4
- Status
- Completed
Conditions
- Hereditary Spastic Paraplegia
Eligibility Criteria
- Sex
- FEMALE
- Age
- 6 Years - 6 Years
- Healthy Volunteers
- Not accepted
Interventions
- D-cycloserine — DRUGPyridoxine also prescribed to help prevent neurologic adverse events related to D-Cycloserine.
Study Details
The overarching objective of this study is to mitigate the neurological decline associated with SPTSSA related Complex Hereditary Spastic Paraplegia
Key Dates
- Start date
- Jul 10, 2024
- Status verified
- Apr 2026
- Primary completion
- Mar 17, 2026
- Completion
- Mar 17, 2026
Study Design
- Enrollment
- 1 participants (actual)
- Allocation
- NA
- Intervention model
- SINGLE_GROUP
- Primary purpose
- TREATMENT
Arms
- Experimental: D-CycloserineD-Cycloserine Administered for Complex Hereditary Spastic Paraplegia
Primary Outcome Measure
Frequency of treatment related serious adverse event [ Time Frame: From baseline to the end of treatment at 1 year ]
Locations (1)
| Facility | City | State | ZIP | Site coordinators |
|---|---|---|---|---|
| Massachusetts General Hospital | Boston | Massachusetts | 02114 | - |
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