Long Term Follow-up Study of Type-1 Gaucher Subjects Post FLT201 Dose (GALILEO-2)
Phase 1
Recruiting
- Conditions
- Gaucher Disease, Type 1
- Registration Number
- NCT06545136
- Lead Sponsor
- Freeline Therapeutics
- Brief Summary
This is a multicenter, long-term, follow-up trial of participants with Gaucher disease type 1 who received FLT201 treatment in a preceding clinical trial. Participants will be followed for 5 years post-treatment.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- RECRUITING
- Sex
- All
- Target Recruitment
- 75
Inclusion Criteria
-
- Participants who have previously received FLT201 (including those who may have required recommencement or initiation of ERT/substrate reduction therapy [SRT]).
-
- Participants able to give full informed consent and able to comply with all requirements of the trial.
Exclusion Criteria
- n/a
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- SINGLE_GROUP
- Primary Outcome Measures
Name Time Method Incidence of treatment-emergent adverse events (TEAEs) (including DLTs) Week 38 to Month 60 Treatment-emergent adverse events (including dose-limiting toxicities), with AEs graded per CTCAE version 5.0 (or later)
- Secondary Outcome Measures
Name Time Method
Trial Locations
- Locations (4)
Lysosomal Rare Disorders Research and Treatment Center
🇺🇸Fairfax, Virginia, United States
Hospital de Clinicas de Porto Alegre (HCPA)
🇧🇷Porto Alegre, Brazil
Hospital Quironsalud Zaragoza
🇪🇸Zaragoza, Spain
Salford Royal Hospital
🇬🇧Salford, United Kingdom
Lysosomal Rare Disorders Research and Treatment Center🇺🇸Fairfax, Virginia, United StatesLauren NollContact703-261-6220lnoll@ldrtc.orgOzlem Goker-AlpanPrincipal Investigator