Observational Safety Study in Women With Neuromyelitis Optica Spectrum Disorder (NMOSD) Exposed to UPLIZNA® During Pregnancy
Eligible age
15+ yrs
Accepts
Women
Locations
1 state
Healthy volunteers
No
See if you qualify for this study
Answer a few quick questions about your location and health. Takes about a minute.
About this study
This is an observational study to monitor female participants exposed to UPLIZNA during pregnancy. This study requires voluntary reporting of pregnancies in female participants with NMOSD exposed to UPLIZNA during pregnancy or within 6 months preceding conception. Pregnancy-related data, potential confounding factors and information related to pregnancy outcome will be collected. The schedule of office visits and all treatment regimens will be determined by the treating healthcare provider. Duration of the study is 10 years, at minimum.
Sponsor: Amgen
You may qualify if…
- ✓ Provide informed consent
- ✓ Are a female of reproductive potential with a confirmed or suspected diagnosis of NMOSD
- ✓ Have been exposed to UPLIZNA during pregnancy as defined by receipt of any dose during pregnancy or within 6 months preceding conception
- ✓ Note: Other Protocol Defined Inclusion/Exclusion Criteria Apply
Where it's recruiting
Aurora
Source: ClinicalTrials.gov · NCT05909761 · last updated 2026-08-31