MedPath

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
    1. Participants who have previously received FLT201 (including those who may have required recommencement or initiation of ERT/substrate reduction therapy [SRT]).
    1. 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
NameTimeMethod
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
NameTimeMethod

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 States
Lauren Noll
Contact
703-261-6220
lnoll@ldrtc.org
Ozlem Goker-Alpan
Principal Investigator

MedPath

Empowering clinical research with data-driven insights and AI-powered tools.

© 2025 MedPath, Inc. All rights reserved.