Personalized Antisense Oligonucleotide Therapy for A Single Participant With CHCHD10 ALS
NCT ID: NCT06392126
Last Updated: 2025-08-05
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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ACTIVE_NOT_RECRUITING
PHASE1/PHASE2
1 participants
INTERVENTIONAL
2024-04-16
2026-04-30
Brief Summary
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Detailed Description
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Conditions
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Study Design
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NA
SINGLE_GROUP
TREATMENT
NONE
Study Groups
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Open Label
nL-CHCHD-001
Personalized antisense oligonucleotide
Interventions
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nL-CHCHD-001
Personalized antisense oligonucleotide
Eligibility Criteria
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Inclusion Criteria
* Ability to travel to the study site and adhere to study-related follow-up examinations and/or procedures and provide access to participant's medical records.
* Genetically confirmed neurological disorder.
Exclusion Criteria
* Use of an investigational medication within less than 5 half-lives of the drug at enrollment
48 Years
MALE
No
Sponsors
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Mayo Clinic
OTHER
n-Lorem Foundation
OTHER
Responsible Party
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Principal Investigators
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Björn E. Oskarsson, M.D.
Role: PRINCIPAL_INVESTIGATOR
Mayo Clinic
Locations
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Mayo Clinic
Jacksonville, Florida, United States
Countries
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Other Identifiers
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23-011476
Identifier Type: -
Identifier Source: org_study_id
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