Acid sphingomyelinase deficiency
Conditions
Interventions
Drug: Olipudase alfa (GZ402665)
Pharmaceutical form: lyophilized powder, Route of administration: Intravenous (IV) infusion.
Sponsors
Tanaka Tomoyuki
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: The patient is eligible to be included in the study only if the following criteria apply: 1) Adult patient who has been enrolled in, and has completed, Study DFI12712 (ASCEND), a Phase 2/3, multicenter, randomized, double-blind, placebo-controlled, repeat dose study to evaluate the efficacy, safety, pharmacodynamics, and pharmacokinetics of olipudase alfa in patients with ASMD. 2) Patient who is willing and able to provide signed written informed consent. 3) If female and of childbearing potential, patient with a negative urine pregnancy test (beta-HCG) result. 4) If female and of childbearing potential or male and sexually active, patient who is willing to abstain from heterosexual intercourse in accordance with her or his preferred and usual life style, or to use 2 acceptable, effective contraceptive methods, while participating in this study and for 15 days after the last infusion of olipudase alfa.
Exclusion criteria
Exclusion criteria: A patient is excluded from the study if any of the following criteria apply: 1) Any patient with a diagnosis of ASMD who has not participated in Study DFI12712. 2) Any new condition or worsening of an existing condition that, in the opinion of the Investigator, would make the patient unsuitable for enrollment, or could interfere with the patient's participation in or completion of the study. 3) Any systemic hypersensitivity reaction to olipudase alfa in Study DFI12712 that, in the opinion of the Investigator, could indicate that continued treatment with olipudase alfa may present an unreasonable risk. 4) Any patient who, in the opinion of the Investigator, is unable to comply with study requirements. 5) Unwillingness or inability to abstain from alcohol for 1 day prior to and 3 days after each olipudase alfa infusion, for the duration of the study period. 6) Any of the following medical conditions: - Active, serious intercurrent illness which will preclude enrollment until recovery is complete. - Any other serious medical or psychiatric condition that may preclude participation, or circumstances that may interfere with compliance in this study. - Requirement for recurrent dose adjustment of anticoagulation treatment over the last 6 months. - Pregnancy or breastfeeding.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Adverse event | — |
Contacts
Public ContactUnit Clinical
Sanofi K.K.
Outcome results
None listed