This is a prospective multicenter, open-label, dose-escalation trial to assess the safety, tolerability, and pharmacodynamics of 4D-310 following a single IV administration. The study population is comprised of adult males and females with Fabry Disease and cardiac involvement
This is a prospective multicenter, open-label, dose-escalation trial to assess the safety, tolerability, and pharmacodynamics of 4D-310 following a single IV administration. The study population is comprised of adult males and females with Fabry Disease and cardiac involvement
Study Type
INTERVENTIONAL
Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
18
Single IV administration of 4D-310
Royal Melbourne Hospital
Melbourne, Australia
ACTIVE_NOT_RECRUITINGRoyal Perth Hospital
Perth, Australia
ACTIVE_NOT_RECRUITINGWestmead Hospital
Westmead, Australia
NOT_YET_RECRUITINGTaipei Veterans General Hospital
Incidence and severity of adverse events
Incidence and severity of adverse events following a single IV dose of 4D-310intravenous (IV) dose
Time frame: 1 year
This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.
Taipei, Taiwan