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Study identifier: NCT04933552 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

Post-Authorization Safety Study for Assessment of Pregnancy Outcomes in Patients Treated With Mayzent

Condition: Multiple Sclerosis  ·  Sponsor: Novartis Pharmaceuticals

PhaseN/A
Planned participants867
Who can joinFemale, N/A to no upper limit
Healthy volunteersYes

About this study

This study will utilize a prospective, observational, exposure cohort design to examine pregnancy and infant outcomes in women and infants who are exposed to siponimod during pregnancy to treat MS.

This description comes directly from the study's public registry record.

Talk to the study team

Novartis Pharmaceuticals  ·  1-888-669-6682  ·  novartis.email@novartis.com

Diana Johnson  ·  1-877-311-8972  ·  mothertobaby@health.ucsd.edu

Always discuss trial participation with your own doctor first.

Locations (1)

Novartis Investigative SiteLa Jolla, California, United StatesRecruiting

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Source record: clinicaltrials.gov/study/NCT04933552