Saves the questions and what to expect into your notes, next to the visit they belong to.
Keep this study
Lead
Sanofi
Randomized period: the total duration will be up to approximately of 20 months (1 month screening 18 months of treatment and a possible follow-up period of 1 month if no participation in the long-term extension period)
Long-term extension period: the total duration will be from minimum 19 months (18 months of treatment and 1 month of follow-up period) to maximum 46 months (45 months of treatment and 1 month of follow-up period). The maximum total study duration is approximately 5.3 years
Age
18–65
Sex
ALL
Healthy volunteers
Not accepted
You may be eligible if
Male and female participants aged 18 to 65 with previously confirmed diagnosis of Fabry disease and a history of clinical symptoms of Fabry disease.
Participants may be receiving treatment with agalsidase alfa, agalsidase beta, or migalastat, or may be untreated.
Left ventricular hypertrophy.
Contraception for male or female participants: not pregnant or breastfeeding; no sperm donating for male participant.
A signed informed consent must be provided prior to any study-related procedures.
You may not be if
History of transient ischemic attack, stroke, myocardial infarction, heart failure, major cardiovascular surgery or kidney transplantation.
History of seizures currently requiring treatment.
Underlying medical condition that may cause or contribute to left ventricular hypertrophy.
Asymmetric hypertrophy by cardiac MRI at screening if considered by central reader to be not related to Fabry disease.
Advanced cardiac fibrosis, defined as significant late gadolinium enhancement affecting 3 or more segments involving \>50% of myocardial thickness on screening cardiac MRI.
History of clinically significant cardiac arrhythmia. Atrial fibrillation that is well controlled on a stable medical regimen for at least 12 months is not an exclusion if the CHA2DS2-VASc score is 0 for males or 1 for females.
Presence of severe depression as measured by Beck's Depression Inventory (BDI)-II \>28 and/or a history of an untreated, unstable major affective disorder within 1 year of the screening visit.
Patients with hepatitis C, HIV, or hepatitis B infection.
Positive SARS-CoV-2 virus test within 2 weeks of enrollment, or COVID-19 requiring hospitalization within 6 months of enrollment.
History of drug and/or alcohol abuse.
Moderate to severe hepatic impairment.
History of or active hepatobiliary disease.
Liver enzymes (alanine aminotransferase/aspartate aminotransferase) or total bilirubin \>2 times the upper limit of normal.
Strong or moderate inducers or inhibitors of cytochrome P450 CYP3A4 within 14 days or 5 half-lives, whichever is longer, prior to randomization.
Known contraindication to undergoing MRI or known hypersensitivity to gadolinium-based contrast agents.
The above information is not intended to contain all considerations relevant to a potential participation in a clinical trial.
Clareo Health | A Study to Evaluate the Effect of Venglustat Tablets on Left Ventricular Mass Index in Male and Female Adult Participants With Fabry Disease
