A Study to Evaluate Safety and Tolerability of Olipudase Alfa in Pediatric and Adult Participants With Acid Sphingomyelinase Deficiency (ASMD) Who Completed the DFI12712 or the LTS13632 Study in France

Exclusion Criteria

• •Participants are excluded from the study if any of the following criteria apply:
• •Any participant who has not participated in the Study DFI12712 or the Study LTS13632
• •A participant who experienced any systemic hypersensitivity reactions to olipudase alfa in Study DFI12712 or Study LTS13632 which, in the opinion of the Investigator, could indicate that treatment continuation may present an unreasonable risk.
• •The participant, in the opinion of the Investigator, is unable to adhere to the requirements of the study.
• •The participant was unwilling or unable to abstain from alcohol for 1 day prior to and 3 days after each olipudase alfa infusion for the duration of the treatment period.
• •Individuals accommodated in an institution because of regulatory or legal order; prisoners or participants who were legally institutionalized.
• •The participant was concurrently participating in another clinical study of investigational treatment.
• •Any of the following medical conditions:
• •The participant has had any new condition or worsening of an existing condition which, in the opinion of the Investigator, would make the participant unsuitable for enrollment or could interfere with the participant's participating in or completing the study.
• •Requirement for recurrent dose adjustment of anticoagulation treatment over the last 6 months.
• •Pregnancy or breastfeeding.
• •The above information is not intended to contain all considerations relevant to a participant's potential participation in a clinical trial.