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Study identifier: NCT06259669 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

Study to Compare Maternal, Fetal, and Infant Outcomes of Women With Mild to Moderate Atopic Dermatitis Exposed to Ruxolitinib Cream During Pregnancy With an Unexposed Control Population

Condition: Pregnancy Related · Atopic Dermatitis  ·  Sponsor: Incyte Corporation

PhaseN/A
Planned participants958
Who can joinFemale, 15 Years to 50 Years
Healthy volunteersNo

About this study

This observational (enrollment into the registry while the pregnancy is ongoing) study is being conducted to compare the frequency of major congenital malformation (MCM)s among infants of women exposed to ruxolitinib cream during pregnancy with infants of women not exposed to ruxolitinib cream during pregnancy.

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

Talk to the study team

Syneos Health  ·  1.833.917.8791  ·  opzeluracreampregnancyregistry@syneoshealth.com

Incyte Corporation Call Center (US)  ·  1.855.463.3463  ·  medinfo@incyte.com

Always discuss trial participation with your own doctor first.

Locations (1)

Syneos Health (remote site)Morrisville, North Carolina, United StatesRecruiting

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Source record: clinicaltrials.gov/study/NCT06259669