OptumInsight Life Sciences Inc
Eden Prairie, Minnesota, 55344, United States
NCT Number: NCT06133049
The purpose of this retrospective observational cohort study is to assess pregnancy and infant outcomes in three groups: the first is women with multiple sclerosis (MS) who were exposed to ozanimod during pregnancy; the second is women with MS exposed to select other disease-modifying therapies (DMTs) during pregnancy; the third is women with MS not exposed to any DMTs during pregnancy. This study will use data from a large US healthcare claims database.
This study is active but is not currently recruiting participants.
18 year–49 year
Female
Observational
Eden Prairie, Minnesota, 55344, United States
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Women with MS who were exposed to ozanimod during pregnancy
Women with MS exposed to select DMTs other than ozanimod during pregnancy
Women with MS not exposed to any DMTs during pregnancy
Time frame: Up to 11 years
Prevalence of major congenital malformations among infants born to women with MS exposed to ozanimod during the first trimester, and to compare this to the prevalence among each of the two comparator groups of pregnant women (other DMT exposed or NO DMT exposed)
Time frame: Up to 11 years
Time frame: Up to 11 years
Time frame: Up to 11 years
Time frame: Up to 11 years
Time frame: Up to 11 years
Time frame: Up to 11 years
Time frame: Up to 11 years
Time frame: Up to 11 years
Time frame: Up to 11 years
Time frame: Up to 11 years
Time frame: Up to 11 years
Time frame: Up to 11 years
Time frame: Up to 11 years
Bristol-Myers Squibb
Industry
Zeposia (Ozanimod) Pregnancy Study: A Retrospective Observational Study on the Safety of Ozanimod Exposure in Pregnant Women and Their Offspring
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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